PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
23333909-1	2013	A water-soluble polysaccharide (MHP-1) isolated from cultured Mortierella hepiali was obtained by hot-water extraction, DEAE-cellulose 52 anion-exchange, and Sephadex G-25 gel permeation chromatography.	DEAE-Cellulose	120-134	calcium channel, voltage-dependent, P/Q type, alpha 1A subunit	Mus musculus	32-37
21673682-4	2011	METHODS: Proteolysis-inducing factor was purified from the MAC16 tumour using an initial pronase digestion, followed by binding on DEAE cellulose, and the pronase was inactivated by heating to 80 C, before purification of the PIF using affinity chromatography.	DEAE-Cellulose	131-145	Pif	Mus musculus	9-36
20934396-7	2011	NAG molecular forms were determined by DEAE-cellulose chromatography.	DEAE-Cellulose	39-53	O-GlcNAcase	Rattus norvegicus	0-3
20706623-2	2010	A novel sperm motility inhibiting factor (MIF-II) has been purified from caprine epididymal plasma (EP) by Hydroxylapatite gel adsorption chromatography, DEAE-Cellulose ion-exchange chromatography and chromatofocusing.	DEAE-Cellulose	154-168	macrophage migration inhibitory factor	Homo sapiens	42-45
19782660-3	2009	Prolidase isoenzymes (PD I and PD II) were isolated from the rat brain using DEAE cellulose column chromatography.	DEAE-Cellulose	77-91	peptidase D	Rattus norvegicus	0-9
20496344-4	2010	Elution behavior on DEAE-cellulose chromatography and cellulose acetate membrane electrophoresis indicated that the purified GO was highly basic (pI>10.0).	DEAE-Cellulose	20-34	hydroxyacid oxidase 2	Homo sapiens	125-127
19782660-3	2009	Prolidase isoenzymes (PD I and PD II) were isolated from the rat brain using DEAE cellulose column chromatography.	DEAE-Cellulose	77-91	prolyl 4-hydroxylase subunit beta	Rattus norvegicus	22-36
16890468-5	2006	Goat chymosin resolved into three major active peaks, indicating possible heterogeneity when passed through DEAE-cellulose ion exchange column.	DEAE-Cellulose	108-122	chymosin	Bos taurus	5-13
19195858-1	2009	A homodimeric, fructose-binding lectin was isolated from Del Monte bananas by using a protocol that involved ion-exchange chromatography on DEAE-cellulose and SP-Sepharose, and gel filtration by fast protein liquid chromatography on Superdex 75.	DEAE-Cellulose	140-154	lectin	Musa acuminata	32-38
17954255-5	2007	The DPP1-encoded enzyme, commonly referred to as diacylglycerol pyrophosphate phosphatase, is purified from wild-type S. cerevisiae membranes by detergent solubilization with Triton X-100 followed by chromatography with DEAE-cellulose (DE53), Affi-Gel blue, hydroxylapatite, and Mono Q.	DEAE-Cellulose	220-234	bifunctional diacylglycerol diphosphate phosphatase/phosphatidate phosphatase	Saccharomyces cerevisiae S288C	4-8
19874043-3	2009	In the present study, two new water-soluble polysaccharides, named LSP1 and LSP2, were isolated from the active crude polysaccharides by DEAE-cellulose 52 and AB-8 macroporous resin chromatography and tested for their hypoglycemic effects.	DEAE-Cellulose	137-151	lymphocyte specific 1	Mus musculus	67-71
19806892-1	2009	The polysaccharide B3-PS2 was extracted and purified from Herba Scutellariae Barbatae through chromatography of DEAE-cellulose and Sephacryl S-300 column.	DEAE-Cellulose	112-126	taste 2 receptor member 64 pseudogene	Homo sapiens	22-25
16777425-3	2006	The lectin was unadsorbed on DEAE-cellulose but adsorbed on Affi-gel blue gel and CM-cellulose.	DEAE-Cellulose	29-43	LTL	Solanum lycopersicum	4-10
16483546-1	2006	A simple purification protocol, involving ion exchange chromatography on DEAE-cellulose and CM-cellulose and fast protein liquid chromatography-gel filtration on Superdex 75, was employed to isolate a Kunitz-type trypsin inhibitor with antifungal activity and a novel lectin from Pseudostellaria heterophylla roots.	DEAE-Cellulose	73-87	kunitz trypsin protease inhibitor	Glycine max	213-230
16186621-2	2005	The results showed that the highest immobilization efficiencies of LOX, 30.6 and 29.3%, were obtained with DEAE-cellulose and modified Eupergit C250L supports, respectively.	DEAE-Cellulose	107-121	linoleate 9S-lipoxygenase-4	Glycine max	67-70
16272685-8	2005	By purification of the high molecular weight fraction using DEAE-cellulose and Phenyl Sepharose column chromatography, two fractions, designated as proteins A and B, were separated and required for the activity.	DEAE-Cellulose	60-74	prolyl 3-hydroxylase 3	Homo sapiens	148-164
12826576-9	2003	Immunoreactive PP1gamma2 and sds22 from both caudal and caput spermatozoa were found in the flow-through fraction of a DEAE-cellulose column.	DEAE-Cellulose	119-133	protein phosphatase 1 regulatory subunit 7	Homo sapiens	29-34
15377270-1	2004	A procedure for isolation and purification of aspartate aminotransferase from wheat grain includes chromatography on DEAE cellulose, acidification-alkalization, precipitation with protamine sulfate, fractionation with ammonium sulfate, and chromatography on hydroxyapatite.	DEAE-Cellulose	117-131	aspartate aminotransferase, cytoplasmic	Triticum aestivum	46-72
14680963-8	2004	An improved purification procedure for the expressed CYP2E1 involving chromatography on diethylaminoethyl cellulose (DE52), Reactive Red-agarose (type 1000-CL), and hydroxyapatite is also reported.	DEAE-Cellulose	88-115	cytochrome P450 2E1	Oryctolagus cuniculus	53-59
15766740-2	2005	DESIGN AND METHODS: After ultrafiltration and dialysis of the acidic and alkaline urines, the B, A, and A2 forms of NAG were separated by ion-exchange chromatography on DEAE cellulose.	DEAE-Cellulose	169-183	O-GlcNAcase	Homo sapiens	116-119
15766740-5	2005	CONCLUSIONS: The determination of the denoted isoenzymes of urinary NAG after ultrafiltration, dialysis, and chromatographic separation on DEAE cellulose is reliable in a wide range of alkaline pH values of urine.	DEAE-Cellulose	139-153	O-GlcNAcase	Homo sapiens	68-71
12946270-9	2003	PON3 has been purified 177-fold to apparent homogeneity with a final specific activity of 461 units/mg using a method consisting of seven steps: solubilization of the microsomal fraction, hydroxyapatite adsorption, chromatography on DEAE-Sepharose CL-6B, non-specific affinity chromatography on Cibacron Blue 3GA, two DEAE-cellulose steps and a final affinity chromatography on concanavalin A-Sepharose.	DEAE-Cellulose	318-332	paraoxonase 3	Rattus norvegicus	0-4
12729599-2	2003	Diethylaminoethyl cellulose or glass fiber filters impregnated with polyethyleneimine were used to capture the [3H]AAG-Hsp90 complex, and conditions which washed >98% of free [3H]AAG from the filters were developed.	DEAE-Cellulose	0-27	heat shock protein 90 alpha family class A member 1	Homo sapiens	119-124
14971310-1	2003	Lipoxygenase was extracted from African oil bean seed and purified by ammonium sulphate precipitation, gel filtration on Sephadex G-25 and ion-exchange chromatography on DEAE--cellulose column.	DEAE-Cellulose	170-185	linoleate 9S-lipoxygenase-4	Glycine max	0-12
14569304-1	2003	Cathepsin B (EC 3.4.22.1) has been highly purified (14,225 fold) from bovine kidney by a rapid procedure that included the preparation of an enriched lysosomal extract, a selective fractionation with ammonium sulphate, size-exclusion chromatography, two cation-exchange chromatographies, and anion-exchange chromatography on diethylaminoethyl-Sephacel.	DEAE-Cellulose	325-351	cathepsin B	Bos taurus	0-11
12700345-10	2003	Human apoC-IV, isolated from apo VLDL by DEAE-cellulose chromatography and two-dimensional electrophoresis, was identified by microsequencing four tryptic peptides.	DEAE-Cellulose	41-55	apolipoprotein C4	Homo sapiens	6-13
10567247-11	1999	PO ovaries contained increased levels of AKAP80 (AKAP of 80 kDa) bound selectively to R subunits in DEAE-cellulose peak 2 (comprising PKAIIbeta and RIalpha), but not to R subunits in DEAE-cellulose peak 3 (comprising PKAIIalpha, PKAIIbeta and RIIbeta).	DEAE-Cellulose	100-114	A-kinase anchoring protein 1	Homo sapiens	41-45
12054614-1	2002	Two forms of poly(A) polymerase (PAPI and PAPII) from germinated wheat embryos have been resolved on DEAE-cellulose ion-exchange chromatography by a linear gradient of 0-500 mM (NH(4))(2)SO(4).	DEAE-Cellulose	101-115	LTP1	Triticum aestivum	33-37
11515546-1	2001	Alpha-glucosidase III, which was different in substrate specificity from honeybee alpha-glucosidases I and II, was purified as an electrophoretically homogeneous protein from honeybees, by salting-out chromatography, DEAE-cellulose, DEAE-Sepharose CL-6B, Bio-Gel P-150, and CM-Toyopearl 650M column chromatographies.	DEAE-Cellulose	217-231	alpha-glucosidase	Apis mellifera	0-17
12411747-5	2003	A 100-kD protein reactive with antibody against muscle alpha-actinin was purified from the Triton-insoluble cytoskeleton of porcine kidney, by MgCl2 treatment, ammonium sulfate fractionation, and subsequent DEAE-cellulose chromatography and hydroxyapatite chromatography.	DEAE-Cellulose	207-221	actinin alpha 1	Homo sapiens	55-68
11533066-3	2001	The aminopeptidase was partially purified by DEAE-cellulose chromatography and found to be heat stable.	DEAE-Cellulose	45-59	aminopeptidase	Saccharomyces cerevisiae S288C	4-18
11792016-4	2001	Enzyme activity was measured by fluorimetric assay while beta-N-acetylhexosaminidase isoenzymes were separated using DEAE-cellulose chromatography.	DEAE-Cellulose	117-131	O-GlcNAcase	Rattus norvegicus	57-84
11583852-1	2001	Fractionation of Saccharomyces cerevisiae postribosomal extract on DEAE-cellulose revealed two fractions of cAMP-dependent protein kinase (PKA-1 and PKA-2).	DEAE-Cellulose	67-81	cAMP-dependent protein kinase catalytic subunit TPK1	Saccharomyces cerevisiae S288C	139-144
11583852-1	2001	Fractionation of Saccharomyces cerevisiae postribosomal extract on DEAE-cellulose revealed two fractions of cAMP-dependent protein kinase (PKA-1 and PKA-2).	DEAE-Cellulose	67-81	cAMP-dependent protein kinase catalytic subunit TPK2	Saccharomyces cerevisiae S288C	149-154
11137456-1	2000	A prolyl endopeptidase (PE) was purified 83 times from human urine by DEAE-cellulose and Sepharose Mercurial chromatographies.	DEAE-Cellulose	70-84	prolyl endopeptidase	Homo sapiens	2-22
11137456-1	2000	A prolyl endopeptidase (PE) was purified 83 times from human urine by DEAE-cellulose and Sepharose Mercurial chromatographies.	DEAE-Cellulose	70-84	prolyl endopeptidase	Homo sapiens	24-26
10567247-11	1999	PO ovaries contained increased levels of AKAP80 (AKAP of 80 kDa) bound selectively to R subunits in DEAE-cellulose peak 2 (comprising PKAIIbeta and RIalpha), but not to R subunits in DEAE-cellulose peak 3 (comprising PKAIIalpha, PKAIIbeta and RIIbeta).	DEAE-Cellulose	100-114	PEAK1 related, kinase-activating pseudokinase 1	Homo sapiens	115-121
10509629-6	1999	PKA was eluted from DEAE-cellulose column with a linear NaCl gradient.	DEAE-Cellulose	20-34	protein kinase cAMP-activated catalytic subunit alpha	Rattus norvegicus	0-3
10604879-1	1999	A unique enzyme, MMA(V) reductase, has been partially purified from rabbit liver by using DEAE-cellulose, carboxymethylcellulose, and red dye ligand chromatography.	DEAE-Cellulose	90-104	glutathione S-transferase omega 2	Homo sapiens	17-33
9886885-2	1998	METHODS: Soluble urinary NEP was purified from human urine using a DEAE-cellulose Cellex D column and gel filtration on an AcA-44 column.	DEAE-Cellulose	67-81	membrane metalloendopeptidase	Homo sapiens	25-28
10434065-2	1999	They were referred to as HXM-A and HXM-B based on their order of elution from a DEAE-cellulose column.	DEAE-Cellulose	80-94	acyl-CoA synthetase medium chain family member 2B	Homo sapiens	25-30
10510735-3	1999	An additional minor enzyme form was found in some premature newborns, which eluted from the DEAE-cellulose column at a higher concentration of NaCl than Hex A and, like this isoenzyme, is able to hydrolyse 4-methylumbellipheryl-2-acetamido-2-deoxy-beta-D-glucopyranoside-6 -sulphate, which would suggest that it has alpha subunits in its molecule.	DEAE-Cellulose	92-106	hexosaminidase subunit alpha	Homo sapiens	153-158
10216966-1	1999	Cytochrome b5 was purified from detergent solubilized sheep liver microsomes by using three successive DEAE-cellulose, and Sephadex G-100 column chromatographies.	DEAE-Cellulose	103-117	cytochrome b5	Ovis aries	0-13
10216966-9	1999	NADH-cytochrome b5 reductase was also partially purified from the same source, detergent solubilized sheep liver microsomes, by using two successive DEAE-cellulose, and 5"-ADP-agarose affinity column chromatographies.	DEAE-Cellulose	149-163	cytochrome b5	Ovis aries	5-18
10643050-7	1999	NF1-rich nuclear protein fraction was purified from the rat liver nuclear extract by DEAE-cellulose and heparin-sepharose chromatography.	DEAE-Cellulose	85-99	neurofibromin 1	Rattus norvegicus	0-3
10355743-5	1999	PP2A multiple forms (2A0, 2A1, 2A2), separated by DEAE-cellulose chromatography and immunoblot analysis of PP2A catalytic subunit, also showed similar differences in these two HBC cell types.	DEAE-Cellulose	50-64	protein phosphatase 2 phosphatase activator	Homo sapiens	0-4
10036768-3	1999	The hSOD1 was purified from the cultured yeast by ammonium sulfate-methanol extraction and DEAE-cellulose column chromatography.	DEAE-Cellulose	91-105	superoxide dismutase 1	Homo sapiens	4-9
9359408-2	1997	Recombinant glycine N-methyltransferase was purified to homogeneity by DEAE-cellulose and gel-filtration chromatography, with a yield of more than 80 mg of pure enzyme from a 1 litre culture.	DEAE-Cellulose	71-85	glycine N-methyltransferase	Rattus norvegicus	12-39
9405398-2	1997	p37 was expressed as a glutathione S-transferase fusion protein and was purified to homogeneity by silver staining using glutathione-agarose, Sephacryl S-200, and DEAE-cellulose chromatography.	DEAE-Cellulose	163-177	nucleoporin 37	Homo sapiens	0-3
9463896-1	1997	The effect of in-place regeneration on equilibrium and kinetic characteristics of the adsorption of bovine serum albumin to a DEAE-cellulose anion exchanger has been determined.	DEAE-Cellulose	126-140	albumin	Homo sapiens	107-120
9695028-1	1998	Two forms of cytochrome b5 were purified from detergent solubilized sheep lung microsomes by three successive DEAE-cellulose, Sephadex G-100 and Sephadex G-200 column chromatographies.	DEAE-Cellulose	110-124	cytochrome b5	Ovis aries	13-26
11063004-2	1998	When the tissues were cultured in the presence of [35-S]methionine/cysteine, metabolically labeled COMP was purified from the culture media and from tissue extracts by DEAE-cellulose gel chromatography.	DEAE-Cellulose	168-182	cartilage oligomeric matrix protein	Homo sapiens	99-103
9367184-6	1997	As a result, it was revealed that the Tg fraction eluted at higher ionic strength from a DEAE-cellulose column is apt to contain more of each iodoamino acid, as well as total content of iodine, larger negative zeta-potential, conforming to sialic acid content in the Tg molecule and to a higher content of di-sialo-bi-antennary complex and to high mannose type oligosaccharides.	DEAE-Cellulose	89-103	thyroglobulin	Homo sapiens	38-40
9399577-2	1997	The method for m-calpain measurement was modified: washing of the DEAE-cellulose column with 0.18 M NaCl instead of 0.15 M NaCl increased the m-calpain activity 12.5-fold.	DEAE-Cellulose	66-80	calpain 2	Rattus norvegicus	15-24
9399577-2	1997	The method for m-calpain measurement was modified: washing of the DEAE-cellulose column with 0.18 M NaCl instead of 0.15 M NaCl increased the m-calpain activity 12.5-fold.	DEAE-Cellulose	66-80	calpain 2	Rattus norvegicus	142-151
9299285-5	1997	Cardiac PKA was extracted and partially purified by acid precipitation, ammonium sulfate fractionation, and DEAE-cellulose chromatography.	DEAE-Cellulose	108-122	protein kinase cAMP-activated catalytic subunit alpha	Rattus norvegicus	8-11
9299285-6	1997	PKA was eluted from DEAE-cellulose column with a linear NaCl gradient.	DEAE-Cellulose	20-34	protein kinase cAMP-activated catalytic subunit alpha	Rattus norvegicus	0-3
8974082-4	1996	The lower molecular weight band corresponded with a component of constitutive PKC activity eluting from DEAE cellulose that was defined by inhibition of basal activity with GF 109203X or H7.	DEAE-Cellulose	104-118	protein kinase C, alpha	Mus musculus	78-81
9095576-3	1997	Isolated NC from mammalian urine, revealed at least 4 isoforms of NC (we call these isoforms NC-A, NC-B, NC-C, and NC-D in the order of elution) during DEAE cellulose column chromatography with a linear gradient of NaCl elution step.	DEAE-Cellulose	152-166	CEA cell adhesion molecule 6	Homo sapiens	93-97
9249915-5	1997	Cardiac PKA was extracted and partially purified by acid precipitation, ammonium sulfate fractionation, and DEAE-cellulose chromatography.	DEAE-Cellulose	108-122	protein kinase cAMP-activated catalytic subunit alpha	Rattus norvegicus	8-11
9249915-6	1997	PKA was eluted from DEAE-cellulose column with a linear NaCl gradient.	DEAE-Cellulose	20-34	protein kinase cAMP-activated catalytic subunit alpha	Rattus norvegicus	0-3
8995217-4	1997	To further understand the signaling pathway of MAPKAP kinase 2, we have purified p60 from a heat-treated neutrophil lysate by DEAE-cellulose chromatography and SDS-polyacrylamide gel electrophoresis.	DEAE-Cellulose	126-140	sequestosome 1	Homo sapiens	81-84
8665801-1	1996	Retinol-binding protein (RBP) was purified from Day 60 porcine allantoic fluid by a combination of diethylaminoethyl cellulose, G-100 Sephadex, G-50 Sephadex, Phenyl-Sepharose, and Reactive Green 19-dye-agarose chromatography.	DEAE-Cellulose	99-126	retinol binding protein 4	Homo sapiens	25-28
8756701-4	1996	When fibrinogen is purified from plasma, the factor XIII zymogen (A2B2) copurifies with it and is found only in the peak 2 fibrinogen when this fraction is separated from peak 1 fibrinogen by ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	223-237	fibrinogen beta chain	Homo sapiens	5-15
8984897-8	1996	DAO of pea seedlings and pig liver is prepared by way of tissue disruption with homogenization, centrifugation, fractionation with ammonium sulfate, precipitation of inert components, column electrophoresis, and DEAE-cellulose column chromatography.	DEAE-Cellulose	212-226	amine oxidase copper containing 1	Sus scrofa	0-3
7599175-1	1995	Phospholipase A2 (PLA2) activity in the soluble fraction of rat kidney yielded three peaks on DEAE cellulose column chromatography.	DEAE-Cellulose	94-108	phospholipase A2 group IB	Rattus norvegicus	18-22
8624849-3	1996	Two phosvitin phosphatase activities, termed Phosvitin Phosphatase 1 and 2 (PvP1, PvP2), which show acidic pH optima were resolved from the 33,000g supernatant fraction from rat brain by a procedure employing successive DEAE-cellulose, Sepharose 6B, second DEAE-cellulose and FPLC/Superose 6 chromatography steps.	DEAE-Cellulose	220-234	casein kinase 2 beta	Rattus norvegicus	4-13
8624849-3	1996	Two phosvitin phosphatase activities, termed Phosvitin Phosphatase 1 and 2 (PvP1, PvP2), which show acidic pH optima were resolved from the 33,000g supernatant fraction from rat brain by a procedure employing successive DEAE-cellulose, Sepharose 6B, second DEAE-cellulose and FPLC/Superose 6 chromatography steps.	DEAE-Cellulose	220-234	casein kinase 2 beta	Rattus norvegicus	45-54
8624849-3	1996	Two phosvitin phosphatase activities, termed Phosvitin Phosphatase 1 and 2 (PvP1, PvP2), which show acidic pH optima were resolved from the 33,000g supernatant fraction from rat brain by a procedure employing successive DEAE-cellulose, Sepharose 6B, second DEAE-cellulose and FPLC/Superose 6 chromatography steps.	DEAE-Cellulose	257-271	casein kinase 2 beta	Rattus norvegicus	4-13
8624849-3	1996	Two phosvitin phosphatase activities, termed Phosvitin Phosphatase 1 and 2 (PvP1, PvP2), which show acidic pH optima were resolved from the 33,000g supernatant fraction from rat brain by a procedure employing successive DEAE-cellulose, Sepharose 6B, second DEAE-cellulose and FPLC/Superose 6 chromatography steps.	DEAE-Cellulose	257-271	casein kinase 2 beta	Rattus norvegicus	45-54
8547318-6	1995	Using the pT7-7 expression vector, EF-1 beta was expressed in Escherichia coli and purified to apparent homogeneity by chromatography on DEAE-cellulose and FPLC on Superose 12 and Mono Q.	DEAE-Cellulose	137-151	elongation factor 1-beta	Oryctolagus cuniculus	35-44
8857186-1	1996	A DEAE-cellulose stationary phase in a rolled configuration was used to separate recombinant secretory leukocyte protease inhibitor (rSLPI) from denaturants and reducing agents (3 M guanidine-HCl and 5 mM DTT) in less than 5 min to promote refolding of the protein to an active form.	DEAE-Cellulose	2-16	secretory leukocyte peptidase inhibitor	Rattus norvegicus	133-138
7496999-1	1995	Chromatography of lung microsomal cytochrome b5 obtained from DEAE-cellulose columns, yielded two distinct cytochrome b5 fractions.	DEAE-Cellulose	62-76	cytochrome b5 type A	Homo sapiens	34-47
7599175-1	1995	Phospholipase A2 (PLA2) activity in the soluble fraction of rat kidney yielded three peaks on DEAE cellulose column chromatography.	DEAE-Cellulose	94-108	phospholipase A2 group IB	Rattus norvegicus	0-16
7599150-1	1995	A heat-stable wheat protein (WP) that is a good substrate for wheat embryo Ca(2+)-dependent protein kinase (CDPK) was purified from wheat embryo by a procedure involving batchwise anion exchange chromatography on DEAE-cellulose (DE52), passage through Phenyl-Sepharose CL-4B, heat and acid treatment and anion exchange HPLC on a DEAE-5PW column.	DEAE-Cellulose	213-227	calcium-dependent protein kinase 19	Triticum aestivum	75-106
7601155-4	1995	After ligation, the covalently closed substrate was used to follow an 1800-fold purification of the mouse X-solvase (EMX1) from crude nuclear extracts by chromatography on DEAE-cellulose, MonoQ and heparin-Sepharose.	DEAE-Cellulose	172-186	empty spiracles homeobox 1	Mus musculus	117-121
7599150-1	1995	A heat-stable wheat protein (WP) that is a good substrate for wheat embryo Ca(2+)-dependent protein kinase (CDPK) was purified from wheat embryo by a procedure involving batchwise anion exchange chromatography on DEAE-cellulose (DE52), passage through Phenyl-Sepharose CL-4B, heat and acid treatment and anion exchange HPLC on a DEAE-5PW column.	DEAE-Cellulose	213-227	calcium-dependent protein kinase 19	Triticum aestivum	108-112
7876565-5	1995	First, the IgE-enriched DEAE-cellulose chromatography fraction was incubated in a batch mode with two alpha hIgE-Fc MAbs (HP6029, HP6061) coupled to CNBr-Sepharose, CL-4B.	DEAE-Cellulose	24-38	immunoglobulin heavy constant epsilon	Homo sapiens	11-14
7544696-2	1995	The alpha 2-M, with a purity of more than 90% and subunit molecular weight of 185kDa, was isolated by ammonium sulfate fractionated precipitation from human blood plasma and purified by DEAE cellulose DE52 column chromatography.	DEAE-Cellulose	186-200	alpha-2-macroglobulin	Homo sapiens	4-13
7986089-3	1994	Cytochrome b5 was purified by a two-column procedure, anion exchange chromatography using DEAE-cellulose, and hydrophobic chromatography on phenyl-Sepharose.	DEAE-Cellulose	90-104	cytochrome b5 type A	Rattus norvegicus	0-13
7803470-1	1994	Two peaks of methionine adenosyltransferase (MAT) activity from human erythrocytes were partially purified on a DEAE-cellulose column.	DEAE-Cellulose	112-126	methionine adenosyltransferase 1A	Homo sapiens	13-43
7803470-1	1994	Two peaks of methionine adenosyltransferase (MAT) activity from human erythrocytes were partially purified on a DEAE-cellulose column.	DEAE-Cellulose	112-126	methionine adenosyltransferase 1A	Homo sapiens	45-48
7986089-6	1994	NADH-cytochrome b5 oxidoreductase was purified by a three-column procedure, DEAE-cellulose, hydroxylapatite, and ADP-agarose.	DEAE-Cellulose	76-90	cytochrome b5 type A	Rattus norvegicus	5-18
7827502-3	1994	Proteolytic treatment of the ammonium sulfate fraction of bacterial lysates with endoproteinase Xa liberated CBS which could then be separated from its fusion partner by DEAE-cellulose chromatography.	DEAE-Cellulose	170-184	cystathionine beta-synthase	Homo sapiens	109-112
7947757-1	1994	A Xenopus laevis casein kinase II-like activity copurified with X. laevis DNA topoisomerase I activity during chromatography on DEAE-cellulose, phosphocellulose, and hydroxylapatite, but the two activities were resolved by chromatography on DNA-agarose [Kaiserman, H. B., Ingebritsen, T. S., & Benbow, R. M. (1988) Biochemistry 27, 3216-3222].	DEAE-Cellulose	128-142	DNA topoisomerase I, gene 1 L homeolog	Xenopus laevis	74-93
8093029-2	1994	PGD synthase was purified from human CSF approximately 8-fold to apparent homogeneity in a yield of 6% by ammonium sulfate fractionation followed by column chromatographies on phenyl-Sepharose and DEAE-cellulose.	DEAE-Cellulose	197-211	phosphoglycerate dehydrogenase	Homo sapiens	0-3
8038221-3	1994	Recombinant RI beta eluted from DEAE-cellulose with a salt concentration (of 0.075 M) equivalent to its elution position from soluble mouse brain extracts with catalytic subunit-free RI alpha.	DEAE-Cellulose	32-46	protein kinase, cAMP dependent regulatory, type I beta	Mus musculus	12-19
8088413-1	1994	Cytochrome b5 was partially purified from sheep lung microsomes in the presence of detergents Emulgen 913 and cholate by three consecutive DEAE-cellulose and Sephadex G-100 gel filtration chromatographies.	DEAE-Cellulose	139-153	cytochrome b5	Ovis aries	0-13
8074672-0	1994	Purification and characterization of protein kinase C from a higher plant, Brassica campestris L. Protein kinase C (PKC) was partially purified from Brassica campestris L., by successive chromatographies on DEAE-cellulose membrane, hydroxyapatite and phenyl-5PW columns.	DEAE-Cellulose	207-221	proline rich transmembrane protein 2	Homo sapiens	116-119
8141763-7	1994	The enzyme activity responsible for the cleavage of bovine CGA co-chromatographed on DEAE-cellulose with the type-2 proinsulin endopeptidase and with PC2 immunoreactivity.	DEAE-Cellulose	85-99	chromogranin A	Bos taurus	59-62
7941742-16	1994	The PPH3-protein was also identified by chromatography of extracts from S. cerevisiae on DEAE-cellulose.	DEAE-Cellulose	89-103	phosphoprotein phosphatase PP4 catalytic subunit PPH3	Saccharomyces cerevisiae S288C	4-8
8089094-1	1994	Three molecular species of Mg(2+)-dependent protein phosphatase (MPPs-1, -2, and -3) were isolated by DEAE cellulose column chromatography and gel filtration from an extract of Saccharomyces cerevisiae.	DEAE-Cellulose	102-116	MAGUK p55 scaffold protein 3	Homo sapiens	65-83
8040350-2	1994	Bovine pepsinogen was purified from abomasum by ammonium sulphate precipitation and ionic exchange chromatography on DEAE-cellulose and Mono Q columns.	DEAE-Cellulose	117-131	pepsin II-2/3	Oryctolagus cuniculus	7-17
8118427-1	1993	A soluble protein kinase (PK) was purified from bovine and human follicular fluids (FF) by ultrafiltration through a PM-10 membrane followed by chromatography on heparin-agarose, DEAE-cellulose and cellulose phosphate columns.	DEAE-Cellulose	179-193	protein kinase cAMP-activated catalytic subunit beta	Bos taurus	10-24
8054853-3	1994	Recombinant rat calretinin was cleaved on the column by thrombin, eluted, and purified to homogeneity using DEAE-cellulose chromatography.	DEAE-Cellulose	108-122	calbindin 2	Rattus norvegicus	16-26
8294420-2	1994	Phosphodiester alpha-GlcNAcase, a membrane-bound enzyme, has been purified about 3,000-fold from bovine liver to apparent homogeneity using detergent solubilization, fractionation on DEAE-cellulose, affinity chromatography on lectin-Sepharose columns, gel filtration, and sodium dodecyl sulfate-polyacrylamide gel electrophoresis.	DEAE-Cellulose	183-197	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	Bos taurus	0-30
7510477-2	1994	The alpha 1-macroglobulin-proteinase complex endocytosed into rat liver lysosomes was purified by a series of column chromatographic steps on concanavalin A-Sepharose, Sephacryl S-300, DEAE-cellulose and TSK gel DEAE-5PW columns.	DEAE-Cellulose	185-199	pregnancy-zone protein	Rattus norvegicus	4-25
8118427-1	1993	A soluble protein kinase (PK) was purified from bovine and human follicular fluids (FF) by ultrafiltration through a PM-10 membrane followed by chromatography on heparin-agarose, DEAE-cellulose and cellulose phosphate columns.	DEAE-Cellulose	179-193	protein kinase cAMP-activated catalytic subunit beta	Bos taurus	26-28
8302290-2	1993	In the present study catalase was extracted and purified 330-fold from goat lung by acetone fractionation and successive chromatographies on DEAE-cellulose, Sephadex G-200, Blue Sepharose CL-6B and Ultrogel AcA-34.	DEAE-Cellulose	141-155	catalase	Capra hircus	21-29
8080473-1	1993	A 7.5-kDa heat- and acid-stable rat brain protein kinase C (PKC) substrate was purified to near homogeneity by a two-step procedure using DEAE-cellulose and hydroxylapatite column chromatography.	DEAE-Cellulose	138-152	protein kinase C, alpha	Rattus norvegicus	60-63
8361955-2	1993	The growth hormone-like substance was not adsorbed on Concanavalin A-Sepharose nor DEAE-cellulose, but could be purified by gel filtration on Sephadex G-50.	DEAE-Cellulose	83-97	gonadotropin releasing hormone receptor	Rattus norvegicus	4-18
8267882-3	1993	Through the 3 stages of purification, i.e. concentration by DEAE-cellulose column chromatography, hydrophobic chromatography on phenyl-sepharose and Mono Q fast protein liquid chromatography, the recombinant truncated M-CSF was purified as to exhibit a specific activity of 1.02 x 10(7) units/mg of protein.	DEAE-Cellulose	60-74	colony stimulating factor 1	Homo sapiens	218-223
8498566-2	1993	We purified an AMP-specific 5"-nucleotidase to homogeneity from the 150,000-g supernatant of dog heart homogenate using phosphocellulose, DEAE-cellulose, and ADP-agarose affinity chromatography.	DEAE-Cellulose	138-152	5'-nucleotidase ecto	Canis lupus familiaris	28-43
8460938-2	1993	Sequential chromatography on octylamino-Sepharose 4B, DEAE-Sephacel, and DEAE-cellulose yielded four isoforms of P450 (A, B, C, and D) with specific contents of 11.0, 9.4, 12.5, and 8.3 nmol of P450/mg protein, respectively.	DEAE-Cellulose	73-87	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	113-133
8386076-2	1993	Bovine serum amine oxidase (BSAO) forms, defined by DEAE-cellulose and hydroxyapatite chromatography, were shown to have different kinetic characteristics with p-dimethylaminobenzylamine as a substrate; there was also some variation in heat sensitivity.	DEAE-Cellulose	52-66	primary amine oxidase, liver isozyme	Bos taurus	7-26
8386076-2	1993	Bovine serum amine oxidase (BSAO) forms, defined by DEAE-cellulose and hydroxyapatite chromatography, were shown to have different kinetic characteristics with p-dimethylaminobenzylamine as a substrate; there was also some variation in heat sensitivity.	DEAE-Cellulose	52-66	primary amine oxidase, liver isozyme	Bos taurus	28-32
22822786-2	1993	The protein has a higher molecular weight than bovine S-antigen which is a highly pathogenic retinal antigen, and was eluted from DEAE-cellulose at a slightly higher NaCl concentration than the concentration at which bovine S-antigen was eluted.	DEAE-Cellulose	130-144	S-antigen visual arrestin	Rattus norvegicus	54-63
8365700-5	1993	Further step, performed by ion-exchange chromatography on DEAE-cellulose, yields a 60-times purified preparation containing a mixture of enzyme components of lysostaphin.	DEAE-Cellulose	58-72	ORF45	Staphylococcus simulans bv. staphylolyticus	158-169
1295560-6	1992	An active fraction retained on DEAE-Cellulose completely lost the inductive activity after incubation with a neutralizing anti-TGF beta antibody.	DEAE-Cellulose	31-45	transforming growth factor, beta 1	Mus musculus	127-135
1333952-1	1992	A mitochondrial endonuclease from Drosophila melanogaster embryos was purified to near homogeneity by successive fractionation with DEAE-cellulose and heparin--avidgel-F, followed by FPLC chromatography on mono S, Superose 12 and a second mono S column.	DEAE-Cellulose	132-146	endonuclease	Escherichia coli	16-28
24202070-4	1993	DEAE-Cellulose chromatography of the extract yielded fractions which showed CHS activity but not deoxychalcone synthase activity, and these fractions were also negative in Western blot analysis.	DEAE-Cellulose	0-14	chalcone synthase	Glycine max	76-79
1291033-3	1992	Sequential chromatography of the salt extract on DEAE-cellulose and phosphocellulose results in an approximately 500-fold increase in specific activity over endogenous NF preparations as measured by 32P-incorporation into the middle molecular mass component of NFs (NF-M).	DEAE-Cellulose	49-63	CCAAT/enhancer binding protein beta	Gallus gallus	266-270
1280270-3	1992	Yolk vitronectin was purified 2,500-fold from chick egg yolk by a combination of hydroxylapatite, DEAE-cellulose, and anti-vitronectin-Sepharose column chromatographies.	DEAE-Cellulose	98-112	vitronectin	Gallus gallus	5-16
16653123-2	1992	DEAE-cellulose ion-exchange chromatography of soluble beta-galactosidase revealed the presence of two isoforms.	DEAE-Cellulose	0-14	beta-galactosidase	Cucumis melo	54-72
1450377-1	1992	Two chloroplast tRNA(Asp) species from barely were purified by chromatography on benzoylated DEAE-cellulose and sequenced.	DEAE-Cellulose	93-107	mitochondrially encoded tRNA glycine	Homo sapiens	16-25
1511747-1	1992	A 20 kDa bifunctional inhibitor of the microbial proteinase, subtilisin, and the alpha-amylase from the larvae of the red flour beetle (Tribolium castaneum) was purified from bran of rice seeds by saline extraction, precipitation with ammonium sulphate, ion-exchange chromatography on DEAE-Cellulose and Toyopearl CM-650, and preparative HPLC on Vydac C18.	DEAE-Cellulose	285-299	alpha-amylase	Tribolium castaneum	81-94
1524434-1	1992	Rat liver fatty acid binding protein (FABP) was purified to homogeneity by procedures including Sephadex G-100 and DEAE-cellulose column chromatographies.	DEAE-Cellulose	115-129	fatty acid binding protein 2	Rattus norvegicus	38-42
1524434-2	1992	FABP was resolved into two major peaks, A and B, by the first DEAE-cellulose column chromatography.	DEAE-Cellulose	62-76	fatty acid binding protein 2	Rattus norvegicus	0-4
1380675-2	1992	In order to demonstrate that PKC in the myelin phosphorylates MBP, PKC was partially purified from rat CNS myelin by solubilization with Triton X-100 followed by a DEAE-cellulose column.	DEAE-Cellulose	164-178	protein kinase C, gamma	Rattus norvegicus	29-32
1335329-7	1992	SDSPAGE showed intact hMR was present in both DEAE-cellulose eluates as three bands between M(r) 110,000-120,000.	DEAE-Cellulose	46-60	mannose receptor C-type 1	Homo sapiens	22-25
1530575-6	1992	Fractions isolated from gastric mucin by chromatography on DEAE-cellulose and Bio-Gel P-2 inhibited ACE with IC50 values ranging from 2 to 16 mM-oligosaccharide.	DEAE-Cellulose	59-73	LOC100188911	Sus scrofa	24-37
1294761-9	1992	Protein kinase A was extracted from the rat livers by acid precipitation and ammonium sulfate fractionation, and then partially purified by DEAE-cellulose.	DEAE-Cellulose	140-154	protein kinase cAMP-activated catalytic subunit alpha	Rattus norvegicus	0-16
1616941-6	1992	Two groups of isoforms of protein kinase C (PKC) were observed in hepatocytes from Zucker rats using DEAE-cellulose column chromatography: PKC 1 and PKC 2.	DEAE-Cellulose	101-115	protein kinase C, alpha	Rattus norvegicus	44-47
1511689-1	1992	Aminopeptidase H was purified from fresh chicken breast muscle by ammonium sulfate fractionation and successive chromatographies on DEAE-cellulose, Ultrogel AcA 34, activated thiol-Sepharose 4B, phenyl-Sepharose CL-4B and DEAE-cellulose again.	DEAE-Cellulose	132-146	bleomycin hydrolase	Gallus gallus	0-16
1511689-1	1992	Aminopeptidase H was purified from fresh chicken breast muscle by ammonium sulfate fractionation and successive chromatographies on DEAE-cellulose, Ultrogel AcA 34, activated thiol-Sepharose 4B, phenyl-Sepharose CL-4B and DEAE-cellulose again.	DEAE-Cellulose	222-236	bleomycin hydrolase	Gallus gallus	0-16
1632801-1	1992	Bovine brain adenosine deaminase cytoplasmatic form was purified about 450 fold by salt fractionation, column chromatography on DEAE-cellulose, octyl-sepharose 4B and affinity chromatography on CH-sepharose 4B 9-(p-aminobenzyl)adenine.	DEAE-Cellulose	128-142	adenosine deaminase	Bos taurus	13-32
1530364-1	1992	An enzyme preparation with affinity to a lysine column was detected from a DEAE-cellulose-adsorbed preparation of human seminal plasma containing plasminogen and plasmin.	DEAE-Cellulose	75-89	plasminogen	Homo sapiens	146-153
1618737-1	1992	Formaldehyde dehydrogenase was purified to electrophoretic and column chromatographic homogeneity from rat liver cytosolic fraction by a procedure which includes ammonium sulfate precipitation, DEAE-cellulose-, hydroxyapatite-, Mono Q-chromatography, and gel filtration.	DEAE-Cellulose	194-208	alcohol dehydrogenase 5 (class III), chi polypeptide	Homo sapiens	0-26
1363453-1	1992	Arylsulfatase A (arylsulfatase sulfohydrolase) EC 3.1.6.1 was purified from rat liver by a procedure consisting of differential centrifugation, Con A-Sepharose and Blue Sepharose chromatography, PBE 94 chromatofocusing, DEAE-cellulose and gel filtration chromatography followed by preparative electrophoresis.	DEAE-Cellulose	220-234	arylsulfatase A	Rattus norvegicus	0-15
1413735-1	1992	A highly thermostable alpha-glucosidase (E C.3.2.1.20) from an extreme thermophile, Thermus thermophilus HB 8, was purified to homogeneous by ammonium sulfate fractionation, DEAE-cellulose chromatography and preparative slab gel electrophoresis.	DEAE-Cellulose	174-188	TTH_RS10165	Thermus thermophilus HB8	22-39
1548485-5	1992	mCANP activity was determined with [14C]azocasein as substrate after removing endogenous CANP inhibitor(s) by ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	141-155	calpain 1	Homo sapiens	1-5
1741371-1	1992	The epsilon subspecies of protein kinase C (epsilon PKC) was purified to near homogeneity from the soluble fraction of rat brain by successive chromatographies on DEAE-cellulose, threonine-Sepharose, phenyl-5PW, Mono Q, heparin-5PW, and hydroxyapatite columns.	DEAE-Cellulose	163-177	protein kinase C, gamma	Rattus norvegicus	52-55
1653025-1	1991	Two main forms of protein kinase C (PKC) activity were found in rat hepatocytes using DEAE-cellulose chromatography: PKC 1 and PKC 2.	DEAE-Cellulose	86-100	protein kinase C, alpha	Rattus norvegicus	36-39
1686872-4	1991	It was separated from PKC by ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	60-74	proline rich transmembrane protein 2	Homo sapiens	22-25
1341917-2	1992	We have fractionated the bradykinin inactivating activity of human urine by stepwise elution chromatography on DEAE-cellulose and recovered 95% of the inactivating activity and 29% of the protein (absorbance at A280 nm).	DEAE-Cellulose	111-125	kininogen 1	Homo sapiens	25-35
1331607-3	1992	To this end we developed a DEAE-cellulose (Cl-) column chromatography procedure for assessing mevalonate kinase in cell extracts that would allow multiple rapid analyses.	DEAE-Cellulose	27-41	mevalonate kinase	Homo sapiens	94-111
1645530-1	1991	Prolyl endopeptidase (EC 3.4.21.26) was purified from human brain by a series of column-chromatographic steps using DEAE-cellulose DE-52, hydroxyapatite, phenyl-Sepharose, Sephacryl S-200 and f.p.l.c.	DEAE-Cellulose	116-130	prolyl endopeptidase	Homo sapiens	0-20
1752026-2	1991	There was an increase in the activity of N-acetyl-beta-D-glucosaminidase (NAG) excreted in the urine and this was characterized by a change in the isoenzyme profiles eluted from DEAE--cellulose.	DEAE-Cellulose	178-193	O-GlcNAcase	Rattus norvegicus	41-72
1752026-2	1991	There was an increase in the activity of N-acetyl-beta-D-glucosaminidase (NAG) excreted in the urine and this was characterized by a change in the isoenzyme profiles eluted from DEAE--cellulose.	DEAE-Cellulose	178-193	O-GlcNAcase	Rattus norvegicus	74-77
2148259-0	1990	Treatment of HL-60 cells with dimethyl sulphoxide inhibits the formation of beta-N-acetylhexosaminidase S. beta-N-Acetylhexosaminidase of HL-60 cells was separated into two main forms, A and S, by chromatography on DEAE-cellulose.	DEAE-Cellulose	215-229	O-GlcNAcase	Homo sapiens	76-103
2026615-2	1991	Dystrophin-glycoprotein complex was isolated from digitonin-solubilized rabbit skeletal muscle membranes by a novel two-step method involving succinylated wheat germ agglutinin (sWGA) chromatography and DEAE-cellulose ion exchange chromatography.	DEAE-Cellulose	203-217	dystrophin	Homo sapiens	0-10
2029785-5	1991	20 from the DEAE-cellulose column consisted of typical AP-A with a molecular weight of approximately 500,000.	DEAE-Cellulose	12-26	glutamyl aminopeptidase	Homo sapiens	55-59
1985950-8	1991	Chromatography on DEAE-cellulose showed that most of the receptor molecules synthesized in hsp90-depleted lysate had lost the capacity to form an oligomeric receptor complex.	DEAE-Cellulose	18-32	heat shock protein 90 alpha family class A member 1	Rattus norvegicus	91-96
1985950-10	1991	Analysis of [35S] methionine-labeled glucocorticoid receptor molecules synthesized in the hsp90-depleted lysate showed the production of polypeptides differing from the expected chromatographic pattern on DEAE-cellulose.	DEAE-Cellulose	205-219	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	37-60
1985950-10	1991	Analysis of [35S] methionine-labeled glucocorticoid receptor molecules synthesized in the hsp90-depleted lysate showed the production of polypeptides differing from the expected chromatographic pattern on DEAE-cellulose.	DEAE-Cellulose	205-219	heat shock protein 90 alpha family class A member 1	Rattus norvegicus	90-95
1985950-11	1991	Upon addition of purified hsp90 to the hsp90-depleted lysate, before translation, the 35S-labeled synthesized receptor fractionated on DEAE-cellulose as an intermediate peak between activated and nonactivated receptor forms.	DEAE-Cellulose	135-149	heat shock protein 90 alpha family class A member 1	Rattus norvegicus	26-31
1985950-11	1991	Upon addition of purified hsp90 to the hsp90-depleted lysate, before translation, the 35S-labeled synthesized receptor fractionated on DEAE-cellulose as an intermediate peak between activated and nonactivated receptor forms.	DEAE-Cellulose	135-149	heat shock protein 90 alpha family class A member 1	Rattus norvegicus	39-44
1825639-2	1991	Rat liver beta-N-acetylhexosaminidase was separated into several different molecular forms by DEAE-cellulose chromatography.	DEAE-Cellulose	94-108	O-GlcNAcase	Rattus norvegicus	10-37
1676408-2	1991	The soluble receptor molecule with molecular weight of approximately 58,000 (Rs1) was initially purified from supernatant of heated lymphocytes through chromatography on Sephadex G-200 and/or DEAE-cellulose.	DEAE-Cellulose	192-206	retinoschisin 1	Homo sapiens	77-80
2081550-2	1990	This protein eluates from DEAE-cellulose with concentrations of KCl known to release actin of other species from the cation.	DEAE-Cellulose	26-40	actin, beta	Gallus gallus	85-90
2287150-3	1990	When KM-102CM and KM-103CM were fractionated by DEAE-cellulose chromatography and treated with antiserum against granulocyte-monocyte colony stimulating factor (GM-CSF) these colony stimulating activity (CSA) and burst promoting activity (BPA) contained in these media were neutralized by the antiserum and thus proved to be basically identical to GM-CSF.	DEAE-Cellulose	48-62	colony stimulating factor 2	Homo sapiens	161-167
1847331-5	1991	The detailed biochemical characterization indicated that this microtubule disruption-activated MAP2 kinase was very similar or identical to the mitogen-activated MAP kinase in the substrate specificity and chromatographic behaviors on phosphocellulose, DEAE-cellulose, gel filtration, and phenyl-Sepharose.	DEAE-Cellulose	253-267	microtubule-associated protein 2	Rattus norvegicus	95-99
1703481-5	1991	This activity eluted from diethylaminoethyl Sephacel at 0.2-0.3 M NaCl, and migrated on Sephacryl S-200 at a mol wt of around 30 k, as described for murine GM- and G-CSF.	DEAE-Cellulose	26-52	colony stimulating factor 3 (granulocyte)	Mus musculus	164-169
1997323-5	1991	65, 948-954] was used to isolate from three DEAE-cellulose chromatographic fractions of diferric rat serotransferrin (rTf) subpopulations having discernible affinities for concanavalin A (ConA).	DEAE-Cellulose	44-58	transferrin	Rattus norvegicus	101-116
1846291-6	1991	A MAP2 kinase has been purified from insulin-treated rat 1 HIRc B cells over 6300-fold by chromatography on Q-Sepharose, phenyl-Sepharose, S-Sepharose, phosphocellulose, QAE-Sepharose, UltrogelAcA54, DEAE-cellulose, and a second Q-Sepharose.	DEAE-Cellulose	200-214	microtubule-associated protein 2	Rattus norvegicus	2-6
1997123-1	1991	The [3H]corticosterone-transcortin complexes from kidney cytosol show elution positions on DEAE-cellulose identical to serum transcortin.	DEAE-Cellulose	91-105	serpin family A member 6	Rattus norvegicus	23-34
2082734-1	1990	The abundant soluble protein of bovine cornea (CSP) was partially purified by chromatographies on Sephacryl S-200, DEAE cellulose and agarose to which mouse anti-CSP monoclonal antibody produced by the hybridoma technique was conjugated.	DEAE-Cellulose	115-129	dnaJ homolog subfamily C member 5	Bos taurus	47-50
2148259-0	1990	Treatment of HL-60 cells with dimethyl sulphoxide inhibits the formation of beta-N-acetylhexosaminidase S. beta-N-Acetylhexosaminidase of HL-60 cells was separated into two main forms, A and S, by chromatography on DEAE-cellulose.	DEAE-Cellulose	215-229	O-GlcNAcase	Homo sapiens	107-134
1692963-8	1990	PK42 and p42 bound to DEAE-cellulose, and both eluted at a salt concentration of 250 mM.	DEAE-Cellulose	22-36	cyclin-dependent kinase 20	Mus musculus	9-12
2174361-3	1990	Both the NGF-activated kinase and the EGF-activated kinase could be partially purified by sequential chromatography on DEAE-cellulose, phenyl-Sepharose and hydroxylapatite, and were identical with each other in their chromatographic behavior, apparent molecular mass (approximately 40 kDa) on gel filtration, substrate specificity, and phosphopeptide-mapping pattern of MAP2 phosphorylated by each kinase.	DEAE-Cellulose	119-133	nerve growth factor	Rattus norvegicus	9-12
2174361-3	1990	Both the NGF-activated kinase and the EGF-activated kinase could be partially purified by sequential chromatography on DEAE-cellulose, phenyl-Sepharose and hydroxylapatite, and were identical with each other in their chromatographic behavior, apparent molecular mass (approximately 40 kDa) on gel filtration, substrate specificity, and phosphopeptide-mapping pattern of MAP2 phosphorylated by each kinase.	DEAE-Cellulose	119-133	epidermal growth factor like 1	Rattus norvegicus	38-41
2265818-1	1990	Rat Liver fatty acid binding protein (FABP) has been purified to homogeneity by the procedures including Sephadex G-100 and DEAE-cellulose column chromatography.	DEAE-Cellulose	124-138	fatty acid binding protein 2	Rattus norvegicus	38-42
2265818-2	1990	FABP was resolved into two peaks of A and B by DEAE-cellulose column chromatography.	DEAE-Cellulose	47-61	fatty acid binding protein 2	Rattus norvegicus	0-4
2168890-1	1990	Acidic fibroblast growth factor (aFGF) receptor was purified from plasma membranes of bovine liver using Triton X-100 extraction, wheat germ lectin-Sepharose 4B gel affinity chromatography, and DEAE-cellulose anion-exchange chromatography.	DEAE-Cellulose	194-208	fibroblast growth factor 1	Bos taurus	33-37
2172248-1	1990	Three isozymes of diacylglycerol kinase (DGK), DGK-I, DGK-II, and DGK-III, were purified from the cytosol of human platelets by successive chromatography on DEAE-cellulose, Ultrogel AcA34, heparin-Sepharose, ATP-agarose, Mono Q, phenyl-Superose, HCA-hydroxyapatite, Wakopak G40, and TSK-3000SW columns.	DEAE-Cellulose	157-171	diacylglycerol kinase beta	Homo sapiens	18-39
2172248-1	1990	Three isozymes of diacylglycerol kinase (DGK), DGK-I, DGK-II, and DGK-III, were purified from the cytosol of human platelets by successive chromatography on DEAE-cellulose, Ultrogel AcA34, heparin-Sepharose, ATP-agarose, Mono Q, phenyl-Superose, HCA-hydroxyapatite, Wakopak G40, and TSK-3000SW columns.	DEAE-Cellulose	157-171	diacylglycerol kinase beta	Homo sapiens	41-44
2226468-9	1990	The EGF-activated M1BK was eluted at about 0.15 M NaCl on a DEAE-cellulose column, while the activated MAP2 kinase was eluted at about 0.1 M NaCl under the conditions used.	DEAE-Cellulose	60-74	epidermal growth factor like 1	Rattus norvegicus	4-7
2167662-2	1990	This property was utilized in a purification procedure for Mu GAM based on guanidine hydrochloride denaturation-renaturation followed by a single DEAE-cellulose chromatographic step.	DEAE-Cellulose	146-160	host-nuclease inhibitor Gam family protein	Escherichia phage Mu	62-65
2337354-1	1990	A novel, alpha-class glutathione S-transferase (GST) isozyme has been isolated from human liver using glutathione (GSH) affinity chromatography, DEAE-cellulose ion-exchange chromatography, and immunoaffinity chromatography.	DEAE-Cellulose	145-159	glutathione S-transferase kappa 1	Homo sapiens	21-46
2337354-1	1990	A novel, alpha-class glutathione S-transferase (GST) isozyme has been isolated from human liver using glutathione (GSH) affinity chromatography, DEAE-cellulose ion-exchange chromatography, and immunoaffinity chromatography.	DEAE-Cellulose	145-159	glutathione S-transferase kappa 1	Homo sapiens	48-51
2396748-1	1990	A procedure for the isolation of glutamate dehydrogenase (GDH) from human liver, which involves the use of ion-exchange chromatography on diethylaminoethyl cellulose and affinity chromatography on guanosine triphosphate conjugated to Sepharose 4B, is described.	DEAE-Cellulose	138-165	glutamate dehydrogenase 1	Homo sapiens	33-56
1978610-1	1990	Gamma-glutamyl transpeptidase was purified to apparent homogeneity from human testis by DEAE cellulose, acetone, precipitation, fractionation by ammonium sulphate, Sephacryl S-200 chromatography, Q-Sepharose chromatography and S-Sepharose chromatography following solubilization of the enzyme by Triton X-100.	DEAE-Cellulose	88-102	inactive glutathione hydrolase 2	Homo sapiens	0-29
2396748-1	1990	A procedure for the isolation of glutamate dehydrogenase (GDH) from human liver, which involves the use of ion-exchange chromatography on diethylaminoethyl cellulose and affinity chromatography on guanosine triphosphate conjugated to Sepharose 4B, is described.	DEAE-Cellulose	138-165	glutamate dehydrogenase 1	Homo sapiens	58-61
1699555-2	1990	In addition to the isolation of 8-, 7-, 6-, 5-, 3-, 2-, 1-, and 0-Gla isomers, we have now purified a variant prothrombin containing 9(8.80) Gla residues by barium citrate adsorption, elution, and finally by DEAE-cellulose and immunoaffinity chromatographies.	DEAE-Cellulose	208-222	coagulation factor II, thrombin	Homo sapiens	110-121
2327787-1	1990	The phenol-sulfating form of phenol sulfotransferase (P-PST) was purified and characterized from human liver cytosol using DEAE-cellulose, Sephacryl S-200, and 3",5"-diphosphoadenosine-agarose affinity chromatography.	DEAE-Cellulose	123-137	sulfotransferase family 1A member 1	Homo sapiens	54-59
2109671-5	1990	Calmodulin (0.1 mumol kg-1 wet weight) was purified by extraction with ethylenediamine tetraacetate-containing buffer, fractionation with trichloroacetic acid and separation by ion exchange chromatography on DEAE-cellulose and by molecular sieving on Ultrogel AcA 54.	DEAE-Cellulose	208-222	calmodulin 1	Homo sapiens	0-10
2107886-3	1990	Using these conditions, NAD synthetase was purified 3,100-fold with a 29% yield using DEAE-cellulose column chromatography, ammonium sulfate fractionation, and dialysis.	DEAE-Cellulose	86-100	NAD synthetase 1	Homo sapiens	24-38
2303419-1	1990	Rhodopsin kinase was purified by sequential chromatography on DEAE-cellulose and blue-Sepharose.	DEAE-Cellulose	62-76	G protein-coupled receptor kinase 1	Bos taurus	0-16
1688711-2	1990	Purification on DEAE-cellulose separated this activity in strains lacking endonuclease I, endonuclease III or exonuclease III.	DEAE-Cellulose	16-30	endonuclease III	Escherichia coli	90-106
1968066-5	1990	Fractionation of solubilized membrane proteins from sensitive and resistant cells on DEAE-cellulose reveals a major protein kinase (PK-1) which exhibits optimal activity in the presence of Mn2+ and histone H1.	DEAE-Cellulose	85-99	pyruvate kinase L/R	Homo sapiens	132-136
2155244-3	1990	At least three distinct fractions with PTPase activity were separated on DEAE cellulose columns, indicating that the enzyme is heterogeneous.	DEAE-Cellulose	73-87	cell division cycle 25C	Homo sapiens	39-45
2154263-5	1990	Ion-exchange analysis of the purified MCR on DEAE-cellulose-52 revealed a single peak in the 0.017 M sodium phosphate region with both RU 26752 and R 5020, but aldosterone dissociated during this procedure.	DEAE-Cellulose	45-59	nuclear receptor subfamily 3, group C, member 2	Rattus norvegicus	38-41
1966645-1	1990	The inactivation of rec BC (D) DNase upon chromatography on DEAE-cellulose was observed.	DEAE-Cellulose	60-74	colicin E8	Escherichia coli	31-36
2105716-1	1990	Significant purification of the ubiquitous cytochrome P-450-A and the strain-specific P-450-B from Drosophila melanogaster has been achieved by sequential chromatography on octylamino-agarose, DEAE-cellulose and hydroxyapatite.	DEAE-Cellulose	193-207	Cytochrome P450-6a2	Drosophila melanogaster	43-59
2105716-1	1990	Significant purification of the ubiquitous cytochrome P-450-A and the strain-specific P-450-B from Drosophila melanogaster has been achieved by sequential chromatography on octylamino-agarose, DEAE-cellulose and hydroxyapatite.	DEAE-Cellulose	193-207	Cytochrome P450-6a2	Drosophila melanogaster	86-93
2297897-3	1990	In this study, we have tried to measure the NAG isoenzymes automatically by use of the recently developed fast protein liquid chromatography (FPLC) system, followed by column chromatography on DEAE cellulose (Mono Q).	DEAE-Cellulose	193-207	O-GlcNAcase	Homo sapiens	44-47
2597194-3	1989	A single form of PST adsorbed on DEAE-cellulose was found in the bull testis, whereas from boar testis two different peaks of PST activity were separated.	DEAE-Cellulose	33-47	sulfotransferase family 1A member 1	Homo sapiens	17-20
2293979-2	1990	PKC activity was measured by incorporation of 32P from [gamma 32P]ATP into histone in the presence of cytosolic and detergent-solubilized membrane fractions purified by diethylaminoethyl cellulose chromatography.	DEAE-Cellulose	169-196	protein kinase C, gamma	Rattus norvegicus	0-3
1694000-2	1990	The recombinant AFP was purified from the yeast lysate by DEAE-cellulose and immunoaffinity chromatography.	DEAE-Cellulose	58-72	alpha-fetoprotein	Rattus norvegicus	16-19
2597194-7	1989	Bull testis PST and boar PST II which were adsorbed on DEAE-cellulose were thermostable, whereas boar PST I was thermolabile.	DEAE-Cellulose	55-69	sulfotransferase family 1A member 1	Homo sapiens	12-15
2597194-7	1989	Bull testis PST and boar PST II which were adsorbed on DEAE-cellulose were thermostable, whereas boar PST I was thermolabile.	DEAE-Cellulose	55-69	sulfotransferase family 1A member 1	Homo sapiens	25-28
2597194-7	1989	Bull testis PST and boar PST II which were adsorbed on DEAE-cellulose were thermostable, whereas boar PST I was thermolabile.	DEAE-Cellulose	55-69	serine peptidase inhibitor Kazal type 1	Homo sapiens	25-30
2559096-2	1989	Elimination of retinoids from either purified CRBP or CRABP holoprotein complex could be performed quantitatively by DEAE-cellulose chromatography without any alteration in the inherent properties of the native proteins.	DEAE-Cellulose	117-131	retinol binding protein 1	Homo sapiens	46-50
2559096-2	1989	Elimination of retinoids from either purified CRBP or CRABP holoprotein complex could be performed quantitatively by DEAE-cellulose chromatography without any alteration in the inherent properties of the native proteins.	DEAE-Cellulose	117-131	cellular retinoic acid binding protein 1	Homo sapiens	54-59
2806260-2	1989	Fatty acid-binding protein (FABP) was purified from rat gastric mucosa by successive Sephadex G-75 chromatography, DEAE-cellulose chromatography and HPLC on an RP-2 (Merck) reversed-phase column.	DEAE-Cellulose	115-129	glutamic-oxaloacetic transaminase 2	Rattus norvegicus	0-26
2553707-2	1989	The major insulin-stimulated activity in rabbit liver is increased 2- to 5-fold compared to material from untreated animals based on DEAE-cellulose profiles.	DEAE-Cellulose	133-147	insulin	Oryctolagus cuniculus	10-17
2553707-4	1989	Chromatography on DEAE-cellulose, S-Sepharose, heptyl-Sepharose, heparin-agarose, and Mono Q results in greater than 20,000-fold purification of the insulin-stimulated enzyme with a 12% recovery.	DEAE-Cellulose	18-32	insulin	Oryctolagus cuniculus	149-156
2591723-4	1989	cGH (fraction B-DE-1) was obtained in pure form from fraction B after DEAE-cellulose chromatography at pH 8.6, with a yield of 2.9 mg/g tissue.	DEAE-Cellulose	70-84	growth hormone	Gallus gallus	0-3
2553122-2	1989	High m-calpain co-purifies with mu-calpain through successive DEAE-cellulose (steep gradient), phenyl-Sepharose, octylamine agarose, and Sephacryl S-300 columns, but elutes after mu-calpain when using a shallow KCl gradient to elute a DEAE-cellulose column.	DEAE-Cellulose	62-76	calpain 2	Gallus gallus	5-14
2553122-2	1989	High m-calpain co-purifies with mu-calpain through successive DEAE-cellulose (steep gradient), phenyl-Sepharose, octylamine agarose, and Sephacryl S-300 columns, but elutes after mu-calpain when using a shallow KCl gradient to elute a DEAE-cellulose column.	DEAE-Cellulose	235-249	calpain 2	Gallus gallus	5-14
2553122-4	1989	High m-calpain, which seems to be a new Ca2+-dependent proteinase, is still heterogeneous after the DEAE-cellulose column eluted with a shallow KCl gradient.	DEAE-Cellulose	100-114	calpain 2	Gallus gallus	5-14
2553122-8	1989	High m-calpain differs from mu- and m-calpain in its elution off DEAE-cellulose columns and its requirement of 3800 microM Ca2+ for one-half maximal activity compared with 5.35 microM Ca2+ for mu-calpain and 420 microM Ca2+ for m-calpain.	DEAE-Cellulose	65-79	calpain 2	Gallus gallus	5-14
2806260-2	1989	Fatty acid-binding protein (FABP) was purified from rat gastric mucosa by successive Sephadex G-75 chromatography, DEAE-cellulose chromatography and HPLC on an RP-2 (Merck) reversed-phase column.	DEAE-Cellulose	115-129	glutamic-oxaloacetic transaminase 2	Rattus norvegicus	28-32
2768278-3	1989	The reaction mixture was separated on diethylaminoethyl cellulose, and a fraction containing the cross-linked complex of calmodulin and myosin light chain kinase was found to have an elevated kinase activity in the absence of Ca2+, which constituted approximately 50% of the maximally stimulated kinase activity of control, and additional kinase activity in the presence of Ca2+, which constituted the remaining 50% of control activity.	DEAE-Cellulose	38-65	calmodulin	Oryctolagus cuniculus	121-131
2575612-2	1989	Aminopeptidase M [EC 3.4.11.2] was purified 772-fold to homogeneity from the microsomal fraction of human liver, with a yield of 18.9%, by a combination of solubilization with 0.5% Triton X-100 and then 1 M urea and chromatography on columns of DEAE-cellulose, hydroxylapatite, Butyl-Toyopearl, and Sephacryl S-300.	DEAE-Cellulose	245-259	alanyl aminopeptidase, membrane	Homo sapiens	0-16
2768278-3	1989	The reaction mixture was separated on diethylaminoethyl cellulose, and a fraction containing the cross-linked complex of calmodulin and myosin light chain kinase was found to have an elevated kinase activity in the absence of Ca2+, which constituted approximately 50% of the maximally stimulated kinase activity of control, and additional kinase activity in the presence of Ca2+, which constituted the remaining 50% of control activity.	DEAE-Cellulose	38-65	myosin light chain kinase, smooth muscle	Oryctolagus cuniculus	136-161
2542371-3	1989	Immunoprecipitation studies and chromatography on DEAE-cellulose and immobilized protein G indicated that the plasma VIP-binding activity was largely due to IgG antibodies.	DEAE-Cellulose	50-64	vasoactive intestinal peptide	Homo sapiens	117-120
2625326-1	1989	The calmodulin has purified by heating, phenyl-Sepharose affinity chromatography, DEAE-cellulose chromatography and Sephadex G50 chromatography from the porcine brain and characterized.	DEAE-Cellulose	82-96	calmodulin 1	Homo sapiens	4-14
2547364-2	1989	Calpains I and II and a few molecular species of calpastatin were identified by chromatographies on DEAE-cellulose and on Ultrogel AcA 34 columns as well as by immunoelectrophoretic blot analysis.	DEAE-Cellulose	100-114	calpastatin	Homo sapiens	49-60
2533975-6	1989	An actin-activated skeletal-muscle myosin Mg-ATPase assay, using skeletal-muscle heavy meromyosin as enzyme and [gamma-32P]-ATP as substrate, demonstrated functional actin in RPE cell extracts after DEAE-cellulose anion exchange chromatography.	DEAE-Cellulose	199-213	actin epsilon 1	Bos taurus	3-8
2747628-3	1989	Immunoblot analysis of platelet 100,000 x g supernatant solution that was fractionated over a DEAE-cellulose column indicated a close correspondence of P-PST activity, as measured by phenol sulfation, and M-PST activity, as assessed by dopamine sulfation, with the 32 and 34 kDa polypeptides, respectively.	DEAE-Cellulose	94-108	sulfotransferase family 1A member 1	Homo sapiens	152-157
2542289-1	1989	Two forms of rat liver aryl hydrocarbon receptor were separated by chromatography on DEAE-cellulose in the presence of molybdate.	DEAE-Cellulose	85-99	aryl hydrocarbon receptor	Rattus norvegicus	23-48
2704389-1	1989	The adenine phosphoribosyltransferase (APRTase) and hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) activities from promastigotes of Leishmania donovani have been purified to homogeneity using ammonium sulfate precipitation, DEAE-cellulose exclusion, and either AMP-agarose (APRTase) or GTP-agarose (HGPRTase) affinity chromatography.	DEAE-Cellulose	235-249	adenine phosphoribosyltransferase	Leishmania donovani	4-37
2704389-1	1989	The adenine phosphoribosyltransferase (APRTase) and hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) activities from promastigotes of Leishmania donovani have been purified to homogeneity using ammonium sulfate precipitation, DEAE-cellulose exclusion, and either AMP-agarose (APRTase) or GTP-agarose (HGPRTase) affinity chromatography.	DEAE-Cellulose	235-249	hypoxanthine-guanine phosphoribosyltransferase	Leishmania donovani	52-98
2704389-1	1989	The adenine phosphoribosyltransferase (APRTase) and hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) activities from promastigotes of Leishmania donovani have been purified to homogeneity using ammonium sulfate precipitation, DEAE-cellulose exclusion, and either AMP-agarose (APRTase) or GTP-agarose (HGPRTase) affinity chromatography.	DEAE-Cellulose	235-249	hypoxanthine-guanine phosphoribosyltransferase	Leishmania donovani	100-108
2704389-1	1989	The adenine phosphoribosyltransferase (APRTase) and hypoxanthine-guanine phosphoribosyltransferase (HGPRTase) activities from promastigotes of Leishmania donovani have been purified to homogeneity using ammonium sulfate precipitation, DEAE-cellulose exclusion, and either AMP-agarose (APRTase) or GTP-agarose (HGPRTase) affinity chromatography.	DEAE-Cellulose	235-249	hypoxanthine-guanine phosphoribosyltransferase	Leishmania donovani	310-318
2486008-1	1989	Cathepsin H was isolated from human placenta by autolysis, acetone fractionation, and chromatography on DEAE-cellulose, Sephadex G-75, hydroxyapatite and concanavalin A-Sepharose.	DEAE-Cellulose	104-118	cathepsin H	Homo sapiens	0-11
2492796-1	1989	The beta-galactosidase (EC 3.2.1.32) of Corynebacterium murisepticum (inducible by lactose and galactose) was purified by successive column chromatography on Sephadex G-200, DEAE-Sephadex A-50 and DEAE-cellulose (DE52).	DEAE-Cellulose	197-211	galactosidase beta 1	Homo sapiens	4-22
2910720-7	1989	Fractionation of the proteins unique to hOF was accomplished with DEAE-cellulose chromatography.	DEAE-Cellulose	66-80	zinc finger and BTB domain containing 20	Homo sapiens	14-16
2910720-7	1989	Fractionation of the proteins unique to hOF was accomplished with DEAE-cellulose chromatography.	DEAE-Cellulose	66-80	zinc finger and BTB domain containing 20	Homo sapiens	40-43
2730640-3	1989	Recombinant S-II was purified from virus-infected cell extracts to near homogeneity by ammonium sulfate fractionation, and chromatographies on DEAE-cellulose and phosphocellulose.	DEAE-Cellulose	143-157	transcription elongation factor A (SII) 1	Mus musculus	12-16
2760564-6	1989	Ion-exchange chromatography on DEAE-cellulose confirms the presence of two different molecular forms of arginine carboxypeptidase activity.	DEAE-Cellulose	31-45	carboxypeptidase N subunit 1	Homo sapiens	104-129
2473101-2	1989	The lactophorin was purified by DEAE-cellulose (pH 7.7), Sephadex G-100, and then Bio Gel A-15m from the component-3 fraction of the proteose-peptone fraction of bovine milk whey.	DEAE-Cellulose	32-46	glycosylation dependent cell adhesion molecule 1	Bos taurus	4-15
2473101-3	1989	The purified lactophorin was separated into seven components by DEAE-cellulose chromatography at pH 8.6.	DEAE-Cellulose	64-78	glycosylation dependent cell adhesion molecule 1	Bos taurus	13-24
2541759-1	1989	Myosin was purified from bovine erythrocytes by chromatography on DEAE-cellulose, Sepharose CL-4B, hydroxylapatite, and DEAE-5PW.	DEAE-Cellulose	66-80	myosin heavy chain 14	Homo sapiens	0-6
2533975-6	1989	An actin-activated skeletal-muscle myosin Mg-ATPase assay, using skeletal-muscle heavy meromyosin as enzyme and [gamma-32P]-ATP as substrate, demonstrated functional actin in RPE cell extracts after DEAE-cellulose anion exchange chromatography.	DEAE-Cellulose	199-213	actin epsilon 1	Bos taurus	166-171
3248623-5	1988	The glucocorticoid receptor was partially purified by affinity chromatography with DOC-Sepharose 6B, and column chromatography with Sephacryl S-300 and DEAE-cellulose in the presence of molybdate throughout the procedure.	DEAE-Cellulose	152-166	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	4-27
2849937-1	1988	Two cellular retinoic acid binding proteins, CRABP I and II, which behaved differently on a DEAE-cellulose column, were purified from 14-day chick embryos.	DEAE-Cellulose	92-106	cellular retinoic acid binding protein 1	Gallus gallus	45-59
3180078-6	1988	By DEAE-cellulose chromatography, the purified mucin was found to be heterogeneous, with three major components that had small differences in carbohydrate composition.	DEAE-Cellulose	3-17	LOC100508689	Homo sapiens	47-52
3220921-4	1988	Instead of a normal ion-exchange resin, a DEAE-cellulose, covalently linked to a synthetic vinyl polymer, was used (DEAE-Zeta-Prep).	DEAE-Cellulose	42-56	prolyl endopeptidase	Equus caballus	126-130
3200835-3	1988	A specific repressor of ferritin mRNA translation has been partially purified from rabbit reticulocytes by differential ultracentrifugation, ammonium sulfate fractionation, and chromatography on phosphocellulose, DEAE-cellulose, and Sephacryl S-300.	DEAE-Cellulose	213-227	Fer2	Triticum aestivum	24-32
2970846-1	1988	beta-N-Acetylhexosaminidase from mouse tissue was separated into its constituent isoenzymes on DEAE-cellulose and its activity was monitored with 4-methylumbelliferyl-beta-N-acetylglucosamine and 4-methylumbelliferyl-beta-N-acetylglucosamine 6-sulphate.	DEAE-Cellulose	95-109	O-GlcNAcase	Mus musculus	0-27
3234380-1	1988	A practical method for haptoglobin subtyping is described utilizing fast sample preparation by means of batch adsorption to DEAE-cellulose and subsequent isoelectric focusing of reductively cleaved samples.	DEAE-Cellulose	124-138	haptoglobin	Homo sapiens	23-34
3134521-3	1988	Vascular permeability factor activity falls into a molecular weight range of 41,000 to 56,000 D. Activity is bound to hydroxylapatite, carboxymethyl-Sepharose, phenyl-Sepharose, and heparin-Sepharose, whereas little or no activity was bound to diethylaminoethyl-Sephacel.	DEAE-Cellulose	244-270	vascular endothelial growth factor A	Homo sapiens	0-28
2837484-3	1988	Two retinoic acid-binding peaks were resolved at the DEAE-cellulose step, with CRABP-I in the major peak and CRABP-II in the minor peak.	DEAE-Cellulose	53-67	cellular retinoic acid binding protein 1	Rattus norvegicus	79-86
3130982-4	1988	DEAE-cellulose chromatography of cell extracts revealed that HL-60/ADR cells contained 2-fold more PK-C than did the parental cell line.	DEAE-Cellulose	0-14	aldo-keto reductase family 1 member B	Homo sapiens	67-70
3130982-4	1988	DEAE-cellulose chromatography of cell extracts revealed that HL-60/ADR cells contained 2-fold more PK-C than did the parental cell line.	DEAE-Cellulose	0-14	proline rich transmembrane protein 2	Homo sapiens	99-103
2844754-1	1988	Rhodopsin kinase was purified to near homogeneity by affinity binding to light-exposed rod cell outer segment membranes, followed by DEAE-cellulose and hydroxyapatite chromatography.	DEAE-Cellulose	133-147	G protein-coupled receptor kinase 7	Homo sapiens	0-16
3419157-1	1988	The relationship between glucocorticoid receptor subunit dissociation and activation was investigated by DEAE-cellulose and DNA-cellulose chromatography of monomeric and multimeric [3H]triamcinolone acetonide ([3H]TA)-labeled IM-9 cell glucocorticoid receptors.	DEAE-Cellulose	105-119	nuclear receptor subfamily 3 group C member 1	Homo sapiens	25-48
3390155-1	1988	Hydroxymethylbilane synthase from human erythrocytes was purified 47,000-fold to greater than 95% homogeneity and 7.5% yield by a simple and rapid procedure using heat treatment (80 degrees C, in the presence of proteinase inhibitors, to convert one of two chromatographically separable forms into the other), DEAE-cellulose and Cibacron Blue F3G-A-Sepharose chromatographies and Sephadex G-75 gel filtration.	DEAE-Cellulose	310-324	hydroxymethylbilane synthase	Homo sapiens	0-28
3139582-1	1988	A 50.4-fold purification of aminopeptidase is achieved by alcohol precipitation, DEAE-cellulose, CM-cellulose and finally Sephadex G-200 chromatography.	DEAE-Cellulose	81-95	carboxypeptidase Q	Homo sapiens	28-42
2829978-9	1988	Some properties of protein phosphatase T, such as its weak binding to DEAE-cellulose and its high stimulation by protamine as compared to a relatively poor stimulation by histone H1, suggest that it may be similar to subtype 2Ao of protein phosphatase 2A.	DEAE-Cellulose	70-84	protein phosphatase 5, catalytic subunit	Rattus norvegicus	19-40
2832208-2	1988	AD6 inhibited selectively human platelet cyclic GMP phosphodiesterase, which was separated from cyclic AMP phosphodiesterase by DEAE-cellulose chromatography.	DEAE-Cellulose	128-142	AD6	Homo sapiens	0-3
2969264-1	1988	N-Acetyl-beta-D-hexosaminidase A was purified from rat urine by ion-exchange chromatography on DEAE-cellulose, followed by concanavalin A chromatography, and finally by chromatography on 2-acetamido-N-(epsilon-aminocaproyl)-2-deoxy-beta-glucosylamine-Se pharose 4B.	DEAE-Cellulose	95-109	hexosaminidase subunit alpha	Rattus norvegicus	16-32
3135686-1	1988	Colony-stimulating factor (CSF) was partially purified from urine of patients with aplastic anemia using DEAE-cellulose and concanavalin A-Sepharose.	DEAE-Cellulose	105-119	colony stimulating factor 2	Homo sapiens	0-25
3276514-12	1988	Furthermore it was noted that EF-1 beta gamma copurified strongly with tubulin on DEAE-cellulose.	DEAE-Cellulose	82-96	eukaryotic translation elongation factor 1 beta 2	Homo sapiens	30-39
3135686-1	1988	Colony-stimulating factor (CSF) was partially purified from urine of patients with aplastic anemia using DEAE-cellulose and concanavalin A-Sepharose.	DEAE-Cellulose	105-119	colony stimulating factor 2	Homo sapiens	27-30
2902852-1	1988	A cysteine proteinase has been isolated from the virulent strain HM1:IMSS of Entamoeba histolytica by two gel chromatography steps, ion exchange chromatography on DEAE-cellulose and affinity chromatography on organomercurial-Sepharose.	DEAE-Cellulose	163-177	EHI_151440	Entamoeba histolytica HM-1:IMSS	2-21
3347053-3	1988	The activation of the ER was further shown by alteration of the elution profile from DEAE-cellulose.	DEAE-Cellulose	85-99	estrogen receptor 1	Rattus norvegicus	22-24
3348886-1	1988	Purification procedure for dipeptidyl peptidase III (DPP III) from human erythrocytes cytosol, entailing separations on DEAE-cellulose, hydroxylapatite and Sephacryl S-200 column, which gave homogeneous preparation in 35% yield, is described.	DEAE-Cellulose	120-134	dipeptidyl peptidase 3	Homo sapiens	27-51
3348886-1	1988	Purification procedure for dipeptidyl peptidase III (DPP III) from human erythrocytes cytosol, entailing separations on DEAE-cellulose, hydroxylapatite and Sephacryl S-200 column, which gave homogeneous preparation in 35% yield, is described.	DEAE-Cellulose	120-134	dipeptidyl peptidase 3	Homo sapiens	53-60
3061534-1	1988	A possible new enzyme, a cytosolic neutral PTH-degrading enzyme previously described by us, was purified by ammonium sulfate fractionation, Sephadex G-200 column chromatography and DEAE cellulose column chromatography from the 100,000 x g supernatant of rat kidney.	DEAE-Cellulose	181-195	parathyroid hormone	Rattus norvegicus	43-46
3172279-1	1988	The major cytosolic and membrane-associated enkephalin-degrading aminopeptidases were purified in parallel by column chromatography successively on DEAE-cellulose, AH-Sepharose, hydroxylapatite, Sephadex G-200, Affigel Blue, AH-Sepharose, and hydroxylapatite.	DEAE-Cellulose	148-162	proenkephalin	Rattus norvegicus	44-54
3347053-5	1988	The overall recoveries of activated ER following chromatography on DEAE-cellulose were significantly lower than the recoveries of the nonactivated ER, 71 and 85%, respectively.	DEAE-Cellulose	67-81	estrogen receptor 1	Rattus norvegicus	36-38
3237643-1	1988	A rapid large scale purification procedure based on three conventional purification steps, ammonium sulfate fractionation, DEAE cellulose and hydroxylapaptite chromotography yields gram amounts of calmodulin.	DEAE-Cellulose	123-137	calmodulin 1	Homo sapiens	197-207
2892601-4	1987	DPP IV was co-purified with gp108 from the Triton-extract by columns of DEAE-cellulose and Bio-gel A-1.5 m. The ratio of DPP IV activity and gp108 content was nearly constant throughout the purification steps.	DEAE-Cellulose	72-86	dipeptidylpeptidase 4	Rattus norvegicus	0-6
3651501-6	1987	Corticosteroid-binding globulin was purified from pregnancy serum by DEAE-cellulose chromatography followed by steroid affinity chromatography on androstadienolone-17 beta-hemisuccinate-ethylenediamine-AffiGel 10.	DEAE-Cellulose	69-83	corticosteroid-binding globulin	Oryctolagus cuniculus	0-31
3499103-2	1987	Alpha-1-PI was isolated from rat plasma by affinity chromatography on Sepharose-bound anhydrochymotrypsin, DEAE-cellulose anion-exchange, and Sephadex G-150 gel filtration.	DEAE-Cellulose	107-121	serpin family A member 1	Rattus norvegicus	0-10
3109992-1	1987	Aldose reductase was purified from testis of non-diabetic BB rats using DEAE cellulose, hydroxylapatite and sephadex G-100 column chromatography.	DEAE-Cellulose	72-86	aldo-keto reductase family 1 member B1	Rattus norvegicus	0-16
2441756-1	1987	The DEAE-cellulose-purified 4 S form of the rat liver glucocorticoid receptor can associate with cytosolic factors, as evidenced by an alteration of the sedimentation value of the 7-8 S form.	DEAE-Cellulose	4-18	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	54-77
3311146-6	1987	CKI-3 shares the following properties with type I casein kinases: it is retained by CM-Sephadex but not by DEAE-cellulose, and it consists of a monomeric protein having a molecular weight of 38,000.	DEAE-Cellulose	107-121	casein kinase YCK3	Saccharomyces cerevisiae S288C	0-5
2885083-1	1987	Previously a new glucocorticoid receptor (Peak C), which eluted with 0.12 to 0.14 M NaCl from DEAE-cellulose column, was identified in addition to another receptor (Peak B), a classic type of glucocorticoid receptor, which eluted with 0.05 to 0.08 M NaCl.	DEAE-Cellulose	94-108	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	17-40
3571287-6	1987	The transformed 6 S GR was separated on DEAE-cellulose into the 4 S GR (eluting at about 100 mM KCl) while its associated RNA eluted at 0.30-0.45 M KCl.	DEAE-Cellulose	40-54	nuclear receptor subfamily 3, group C, member 1	Mus musculus	20-22
3597346-1	1987	We have identified a 56-kDa fatty acid binding protein in rat renal basolateral membrane and purified it by extraction in nonionic detergent (Triton X-100), followed by gel filtration, DEAE-cellulose chromatography, and affinity chromatography.	DEAE-Cellulose	185-199	glutamic-oxaloacetic transaminase 2	Rattus norvegicus	28-54
3030755-4	1987	This ribosomal protein S6 kinase activity was substantially purified by a combination of phosphocellulose, DEAE-cellulose, Mono Q and heparin-Sepharose chromatography, and some of its characteristics were examined.	DEAE-Cellulose	107-121	40S ribosomal protein S6	Mesocricetus auratus	5-25
3468504-1	1987	Glutamate decarboxylase (GDCase; L-glutamate-1-carboxy-lyase, EC 4.1.1.15) was purified from whole rat brain approximately equal to 1300-fold to apparent homogeneity with a specific activity of 2.4 units per mg of protein by a combination of column chromatographies on DEAE-cellulose, hydroxylapatite, and gel filtration, and preparative nondenaturing polyacrylamide gel electrophoresis.	DEAE-Cellulose	269-283	glutamate-ammonia ligase	Rattus norvegicus	0-23
3035036-2	1987	IR-hCG was extracted using a kaolin-acetone-alcohol concentration and purified by DEAE Cellulose, Sephadex G-100 and DEAE Sephacel column chromatographies according to Nishimura et al.	DEAE-Cellulose	82-96	chorionic gonadotropin subunit beta 5	Homo sapiens	3-6
3468504-1	1987	Glutamate decarboxylase (GDCase; L-glutamate-1-carboxy-lyase, EC 4.1.1.15) was purified from whole rat brain approximately equal to 1300-fold to apparent homogeneity with a specific activity of 2.4 units per mg of protein by a combination of column chromatographies on DEAE-cellulose, hydroxylapatite, and gel filtration, and preparative nondenaturing polyacrylamide gel electrophoresis.	DEAE-Cellulose	269-283	glutamate-ammonia ligase	Rattus norvegicus	25-31
2834593-3	1987	Moreover, calmodulin-dependent phosphodiesterase, and independent phosphodiesterase were separated from crude lens extract using DEAE-cellulose column.	DEAE-Cellulose	129-143	calmodulin	Bos taurus	10-20
3805000-3	1987	However, a single species of Fab with a pI of 7.6 could be isolated in good yield by DEAE-cellulose chromatography, and good crystals were produced by the hanging drop vapor diffusion method.	DEAE-Cellulose	85-99	FA complementation group B	Homo sapiens	29-32
2826314-1	1987	In the longitudinal layer of nonpregnant human myometrium, cyclic nucleotide phosphodiesterase (PDE) activity from the soluble fraction is resolved by DEAE-cellulose chromatography into a single peak which presents no substrate specificity and is calcium-calmodulin-sensitive.	DEAE-Cellulose	151-165	phosphodiesterase 3B	Homo sapiens	59-94
2432942-1	1987	Cellular retinoic acid-binding protein (CRABP) has been purified to homogeneity from human placenta by a series of procedures, including acetone powder extraction, gel filtration on Sephadex G-50, and ion-exchange chromatography on DEAE-cellulose and on SP-Sephadex.	DEAE-Cellulose	232-246	cellular retinoic acid binding protein 1	Homo sapiens	0-38
2432942-1	1987	Cellular retinoic acid-binding protein (CRABP) has been purified to homogeneity from human placenta by a series of procedures, including acetone powder extraction, gel filtration on Sephadex G-50, and ion-exchange chromatography on DEAE-cellulose and on SP-Sephadex.	DEAE-Cellulose	232-246	cellular retinoic acid binding protein 1	Homo sapiens	40-45
2881760-9	1987	Three distinct fractions of hepatic cytochrome P-450 isozyme 2 were obtained when chromatography on DEAE-cellulose was used as the final step in the purification procedure.	DEAE-Cellulose	100-114	cytochrome P450 2B4	Oryctolagus cuniculus	36-62
3539798-3	1987	Neuraminidase produced by GBS strain 122 (serotype III) was purified by a combination of salt fractionation, affinity chromatography with Affi-Gel Blue, ion-exchange chromatography with DEAE-cellulose, and gel filtration on Sephadex G-200.	DEAE-Cellulose	186-200	neuraminidase 1	Bos taurus	0-13
3450871-1	1987	This study analyzes the effect of including molybdate in the elution buffers used in DEAE cellulose chromatography on the fraction of glucocorticoid receptor which elutes as the transformed species.	DEAE-Cellulose	85-99	nuclear receptor subfamily 3 group C member 1	Homo sapiens	134-157
2881817-5	1987	Mobility of testicular soluble PK-C activity in HPLC-DEAE cellulose chromatography was similar to that of the brain enzyme.	DEAE-Cellulose	53-67	protein kinase C, gamma	Rattus norvegicus	31-35
3303039-2	1987	CBR was purified to homogeneity by DEAE-cellulose chromatography, affinity chromatography using Blue-sepharose, followed by gel filtration on Sephacryl S-200.	DEAE-Cellulose	35-49	carbonyl reductase 1	Mus musculus	0-3
3023087-2	1986	Pig platelet gelsolin has been prepared by chromatography on DEAE-cellulose and actin-Sepharose.	DEAE-Cellulose	61-75	GSN	Sus scrofa	13-21
2947632-3	1986	Purification of cardiac alpha-actinin was achieved by chromatography on DEAE-cellulose and hydroxyapatite columns.	DEAE-Cellulose	72-86	actinin alpha 1	Homo sapiens	24-37
2946929-1	1986	LY195115 selectively inhibited the peak III isozyme of cardiac cyclic nucleotide phosphodiesterase (PDE) eluted from DEAE-cellulose columns.	DEAE-Cellulose	117-131	phosphodiesterase 3B	Homo sapiens	63-98
3782139-1	1986	Arachidonate 12-lipoxygenase was purified to near homogeneity from the cytosol fraction of porcine leukocytes by ammonium sulfate fractionation, DEAE-cellulose chromatography, and immunoaffinity chromatography using a monoclonal antibody against the enzyme.	DEAE-Cellulose	145-159	arachidonate 12-lipoxygenase, 12S type	Homo sapiens	0-28
3536083-2	1986	ACAA is a large molecular weight glycoprotein (Mr 790,000 by size chromatography on Sepharose CL-6B) that migrates in the alpha 1 region upon electrophoresis and is eluted from a DEAE-cellulose column at a 0.1 M NaCl concentration.	DEAE-Cellulose	179-193	acetyl-CoA acyltransferase 1	Homo sapiens	0-4
3463246-2	1986	Two forms of PST which were capable of conjugating phenol and a third form which sulfated dopamine were resolved from one another using DEAE-cellulose chromatography.	DEAE-Cellulose	136-150	sulfotransferase family 1A member 1	Homo sapiens	13-16
3756171-1	1986	Eukaryotic protein synthesis initiation factor 2 (eIF-2) from rat liver has been resolved into two subfractions by anion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	148-162	eukaryotic translation initiation factor 2 subunit gamma	Homo sapiens	50-55
3790497-5	1986	RNase A and S protein do not stimulate the conformational change which is associated with activation and is reflected in a shift in the elution profile of receptor complexes from DEAE-cellulose.	DEAE-Cellulose	179-193	ribonuclease A family member 1, pancreatic	Rattus norvegicus	0-7
3019632-4	1986	The unactivated aldosterone-mineralocorticoid receptor complex did not bind to DNA-cellulose, was eluted from DEAE-cellulose at relatively high salt (195 mM KCl) concentration, and had an apparent Stokes radius when chromatographed on Sephacryl S300 of 6.3 nm.	DEAE-Cellulose	110-124	nuclear receptor subfamily 3, group C, member 2	Rattus norvegicus	28-54
3019632-5	1986	After activation, the aldosterone-mineralocorticoid receptor complex had increased affinity for DNA-cellulose and decreased affinity for DEAE-cellulose and appeared as a smaller complex when chromatographed on Sephacryl S300.	DEAE-Cellulose	137-151	nuclear receptor subfamily 3, group C, member 2	Rattus norvegicus	34-60
16664952-1	1986	Adenylate kinase (EC 2.7.4.3) from leaves of maize (Zea mays) was purified to homogeneity using (NH(4))(2)SO(4) fractionation, followed by chromatography on DEAE-cellulose, hydroxyapatite, Sephadex G-75SF, and Green A dye-ligand columns.	DEAE-Cellulose	157-171	Adenylate kinase, chloroplastic	Zea mays	0-16
3800945-5	1986	LDL receptor protein could be readily assayed using the two-antibody procedure in normal human skin fibroblast extracts prepared by bulk-elution from small columns of DEAE-cellulose followed by rapid desalting.	DEAE-Cellulose	167-181	low density lipoprotein receptor	Bos taurus	0-12
3016729-1	1986	Thrombomodulin isolated from rabbit lung was separated by ion-exchange chromatography on DEAE-cellulose into a retarded (acidic) and a nonretarded (nonacidic) fraction.	DEAE-Cellulose	89-103	thrombomodulin	Oryctolagus cuniculus	0-14
3778666-5	1986	However, passage of the 55Fe.HTr (ceruloplasmin) reaction mixture through DEAE-cellulose caused 55-60% of 55Fe to be lost from the protein, although no decrease in absorbance at 465 nm was observed.	DEAE-Cellulose	74-88	telomerase RNA component	Homo sapiens	29-32
3778666-5	1986	However, passage of the 55Fe.HTr (ceruloplasmin) reaction mixture through DEAE-cellulose caused 55-60% of 55Fe to be lost from the protein, although no decrease in absorbance at 465 nm was observed.	DEAE-Cellulose	74-88	ceruloplasmin	Homo sapiens	34-47
3770442-1	1986	Prolactin (PRL) was purified from anterior pituitary glands of adult toad (Bufo japonicus formosus) by extraction of acetone-dried pituitary powder with acid acetone and chromatography on DEAE-cellulose and Sephadex G-100.	DEAE-Cellulose	188-202	prolactin	Bos taurus	11-14
3742818-2	1986	Bile trypsin inhibitor from malignant tumor patients was partially purified by DEAE cellulose ion exchange column chromatography.	DEAE-Cellulose	79-93	cysteine rich secretory protein LCCL domain containing 2	Homo sapiens	5-22
3016961-1	1986	Two forms of soluble phosphodiesterase of cyclic nucleotides separating by DEAE-cellulose ion-exchange chromatography and not only differing in physicochemical and catalytic parameters but also differently regulated by calmodulin are found in the doe myometrium.	DEAE-Cellulose	75-89	calmodulin	Oryctolagus cuniculus	219-229
3700427-5	1986	Calmodulin N-methyltransferase was purified 470-fold with a 33% yield from rat testis cytosol, using ammonium sulfate precipitation and chromatography on DEAE-cellulose, CM-Sepharose, and Sephadex G-100.	DEAE-Cellulose	154-168	calmodulin 1	Rattus norvegicus	0-10
2939882-1	1986	A proteinase inhibitor has been isolated from human colorectal adenocarcinomas by extraction with a low-ionic-strength buffer and a combination of Con A-Sepharose, Sephadex G-200, DEAE-cellulose and chromatofocusing steps.	DEAE-Cellulose	180-194	endogenous retrovirus group K member 18	Homo sapiens	2-12
3753469-1	1986	Mouse brain ornithine decarboxylase (ODC) was purified to near-homogeneity by using (NH4)2SO4 precipitation and chromatography on heparin-Sepharose, pyridoxamine phosphate-agarose and DEAE-cellulose.	DEAE-Cellulose	184-198	ornithine decarboxylase, structural 1	Mus musculus	12-35
3753469-1	1986	Mouse brain ornithine decarboxylase (ODC) was purified to near-homogeneity by using (NH4)2SO4 precipitation and chromatography on heparin-Sepharose, pyridoxamine phosphate-agarose and DEAE-cellulose.	DEAE-Cellulose	184-198	ornithine decarboxylase, structural 1	Mus musculus	37-40
2422811-7	1986	2-5A derivatives which inhibited the activation of RNase L by authentic 2-5A were eluted from DEAE-cellulose with 90 mM KCl.	DEAE-Cellulose	94-108	ribonuclease L	Homo sapiens	51-58
3955807-3	1986	SHBG was measured by a DEAE cellulose filter assay and T by radioimmunoassay.	DEAE-Cellulose	23-37	sex hormone binding globulin	Homo sapiens	0-4
3708020-2	1986	The SRC within the composition of cytosol and purified 2000-fold were characterized by gel filtration of Sephadex G-100 and by DEAE-cellulose chromatography.	DEAE-Cellulose	127-141	SRC proto-oncogene, non-receptor tyrosine kinase	Rattus norvegicus	4-7
3955075-2	1986	pAp was obtained through perchloric acid extraction of the liver followed by two successive DEAE-cellulose chromatographies and an ion-pair high-pressure liquid chromatography.	DEAE-Cellulose	92-106	regenerating family member 3 beta	Rattus norvegicus	0-3
16664628-1	1986	Phosphoenolpyruvate carboxylase (EC 4.1.1.31) was purified to homogeneity with about 29% recovery from immature pods of chickpea using ammonium sulfate fractionation, DEAE-cellulose chromatography, and gel filtration through Sephadex G-200.	DEAE-Cellulose	167-181	phosphoenolpyruvate carboxylase	Cicer arietinum	0-31
4066681-1	1985	Purified human colonic mucin contains six distinct components which may be separated by DEAE-cellulose chromatography.	DEAE-Cellulose	88-102	LOC100508689	Homo sapiens	23-28
3961272-3	1986	On the other hand, granulocyte S1 fractions subjected to noctylamino sepharose 4B and DEAE cellulose column chromatography separately revealed about 11 fold purification of cytochrome P-450.	DEAE-Cellulose	86-100	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	173-189
3712357-0	1986	Molybdate affects glucocorticoid receptor chromatography on DEAE cellulose.	DEAE-Cellulose	60-74	nuclear receptor subfamily 3 group C member 1	Homo sapiens	18-41
3712357-1	1986	How molybdate affects the chromatographic behavior of the glucocorticoid receptor on DEAE cellulose was investigated.	DEAE-Cellulose	85-99	nuclear receptor subfamily 3 group C member 1	Homo sapiens	58-81
3111522-5	1986	IgM antibodies were isolated from serum by column chromatography on Sefadeks G-200 gel and IgG1 and IgG2 by column chromatography on DEAE cellulose.	DEAE-Cellulose	133-147	IgM	Bos taurus	0-3
3517499-8	1986	The 90 kdalton phosphoprotein determines the acidic behavior of the untransformed glucocorticoid receptor on DEAE-cellulose.	DEAE-Cellulose	109-123	nuclear receptor subfamily 3 group C member 1	Homo sapiens	82-105
4076188-1	1985	An actin-polymerization-inhibiting protein, that occurs in crude preparations of vinculin from chicken gizzard, has been purified by DEAE-cellulose and carboxymethyl ion-exchange chromatography.	DEAE-Cellulose	133-147	vinculin	Gallus gallus	81-89
3865533-5	1985	The two physical forms of glucocorticoid receptor were isolated with DEAE cellulose chromatography.	DEAE-Cellulose	69-83	nuclear receptor subfamily 3 group C member 1	Homo sapiens	26-49
4084323-2	1985	A simple and reproducible purification procedure of homogeneous DNA polymerase beta from rat liver is developed, including sedimentation and saline extraction of rat liver chromatin, chromatography of the extract on DEAE-cellulose, phosphocellulose, Gel Blue A, and DNA sepharose.	DEAE-Cellulose	216-230	DNA polymerase beta	Rattus norvegicus	64-83
4083898-1	1985	Aromatase cytochrome P-450 (P-450AROM) was partially purified from human placental microsomes by hydrophobic affinity chromatography using Phenyl-Sepharose and ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	191-205	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	10-26
4083898-1	1985	Aromatase cytochrome P-450 (P-450AROM) was partially purified from human placental microsomes by hydrophobic affinity chromatography using Phenyl-Sepharose and ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	191-205	cytochrome P450 family 19 subfamily A member 1	Homo sapiens	28-37
2935526-5	1985	Actin was removed by ultracentrifugation in the presence of Mg-ATP and finally by column chromatography on DEAE-cellulose.	DEAE-Cellulose	107-121	ACTin	Caenorhabditis elegans	0-5
2999440-1	1985	Human cytomegalovirus-induced DNA polymerase and cellular DNA polymerase alpha were purified by successive chromatography on DEAE-cellulose, phosphocellulose, heparin agarose, and single-stranded DNA agarose columns.	DEAE-Cellulose	125-139	DNA polymerase alpha 1, catalytic subunit	Homo sapiens	58-78
4053015-5	1985	PR was partially purified by phosphocellulose and DEAE cellulose chromatography, and the DEAE eluate was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and photoaffinity labeling with [17 alpha-methyl-3H]promegestone ([3H]R5020).	DEAE-Cellulose	50-64	progesterone receptor	Homo sapiens	0-2
3930326-1	1985	Human aorta, brain, and muscle aldose reductase, partially purified by DEAE-cellulose (DE-52) column chromatography, is activated 2-2.5-fold on incubation with 10 microM each of glucose-6-phosphate, NADPH, and glucose for 20 min at 25 degrees C. The activation of the enzyme was established by following the NADPH oxidation as well as the sorbitol formation using glucose as substrate.	DEAE-Cellulose	71-85	aldo-keto reductase family 1 member B	Homo sapiens	31-47
2935535-5	1985	Fibrinogen purified by chromatography on either DEAE-cellulose or Sepharose-lysine to remove plasminogen was less degraded.	DEAE-Cellulose	48-62	fibrinogen beta chain	Homo sapiens	0-10
3933003-1	1985	Aldose reductase (alditol:NADP+ 1-oxidoreductase, EC 1.1.1.21) has been partially purified from human erythrocytes by DEAE-cellulose (DE-52) column chromatography.	DEAE-Cellulose	118-132	aldo-keto reductase family 1 member B	Homo sapiens	0-16
4085662-1	1985	A new isozyme of Glutathione-S-transferase (GST) with more acidic pI (6.7) than other forms of GST hitherto reported was isolated from rat liver cytosol by consecutive chromatographies on a DEAE cellulose column, lysyl-GSH affinity column and Sephadex G-100 column.	DEAE-Cellulose	190-204	hematopoietic prostaglandin D synthase	Rattus norvegicus	17-42
3877780-1	1985	Leukocyte elastase-inhibitor complexes in porcine blood, I. alpha 1-Proteinase inhibitor was purified from porcine blood by ammonium sulphate and Cibachron Blue-Sepharose fractionation, ion exchange chromatography on DEAE-Cellulose, gel filtration on Sephadex G-25, and zinc chelating chromatography.	DEAE-Cellulose	217-231	serpin family B member 1	Homo sapiens	0-28
3001971-1	1985	The binding protein to platelet activating factor (PAF) was solubilized with 2% Triton X-100 from human platelet membranes and purified approximately 23-fold by sequential chromatography on DEAE-cellulose, CM-cellulose and Sephadex G-200.	DEAE-Cellulose	190-204	PCNA clamp associated factor	Homo sapiens	23-49
3001971-1	1985	The binding protein to platelet activating factor (PAF) was solubilized with 2% Triton X-100 from human platelet membranes and purified approximately 23-fold by sequential chromatography on DEAE-cellulose, CM-cellulose and Sephadex G-200.	DEAE-Cellulose	190-204	PCNA clamp associated factor	Homo sapiens	51-54
4085662-1	1985	A new isozyme of Glutathione-S-transferase (GST) with more acidic pI (6.7) than other forms of GST hitherto reported was isolated from rat liver cytosol by consecutive chromatographies on a DEAE cellulose column, lysyl-GSH affinity column and Sephadex G-100 column.	DEAE-Cellulose	190-204	hematopoietic prostaglandin D synthase	Rattus norvegicus	44-47
4085662-1	1985	A new isozyme of Glutathione-S-transferase (GST) with more acidic pI (6.7) than other forms of GST hitherto reported was isolated from rat liver cytosol by consecutive chromatographies on a DEAE cellulose column, lysyl-GSH affinity column and Sephadex G-100 column.	DEAE-Cellulose	190-204	hematopoietic prostaglandin D synthase	Rattus norvegicus	95-98
4085662-8	1985	The anionic GST-corticosterone complex bound to DNA coupled Sepharose at 25 degrees C and passed through the column at 4 degrees C. Conversely, the complex bound to a DEAE cellulose column at 4 degrees C but passed through at 25 degrees C. These properties of anionic GST are quite similar to those of glucocorticoid receptor of rat liver cytosol reported previously.	DEAE-Cellulose	167-181	hematopoietic prostaglandin D synthase	Rattus norvegicus	12-15
3896404-1	1985	L-Histidine decarboxylase [L-histidine carboxylyase, HDC, EC 4.1.1.22] is an enzyme distinct from L-DOPA decarboxylase [L-aromatic amino acid carboxylyase, DDC, EC 4.1.1.28]: the two decarboxylases from fetal rat liver were completely separated from each other by DEAE-cellulose column chromatography and by affinity chromatography with L-carnosine as a ligand.	DEAE-Cellulose	264-278	histidine decarboxylase	Cavia porcellus	2-25
3861769-1	1985	An arylamine sulfotransferase (PST-M) from human brain cortex that is involved in the formation of O-sulfate esters of monoamines has been purified 272-fold by ammonium sulfate fractionation, gel filtration, DEAE-cellulose ion-exchange chromatography, chromatofocussing, and hydroxyapatite chromatography.	DEAE-Cellulose	208-222	sulfotransferase family 1A member 2	Homo sapiens	3-29
3861769-1	1985	An arylamine sulfotransferase (PST-M) from human brain cortex that is involved in the formation of O-sulfate esters of monoamines has been purified 272-fold by ammonium sulfate fractionation, gel filtration, DEAE-cellulose ion-exchange chromatography, chromatofocussing, and hydroxyapatite chromatography.	DEAE-Cellulose	208-222	sulfotransferase family 1A member 1	Homo sapiens	31-34
3897758-1	1985	Rat kidney membranes were solubilized by Triton X-100 and the CCK-8 degrading peptidases were resolved by chromatography on DEAE-cellulose.	DEAE-Cellulose	124-138	cholecystokinin	Rattus norvegicus	62-65
3896404-1	1985	L-Histidine decarboxylase [L-histidine carboxylyase, HDC, EC 4.1.1.22] is an enzyme distinct from L-DOPA decarboxylase [L-aromatic amino acid carboxylyase, DDC, EC 4.1.1.28]: the two decarboxylases from fetal rat liver were completely separated from each other by DEAE-cellulose column chromatography and by affinity chromatography with L-carnosine as a ligand.	DEAE-Cellulose	264-278	histidine decarboxylase	Rattus norvegicus	53-56
3896404-1	1985	L-Histidine decarboxylase [L-histidine carboxylyase, HDC, EC 4.1.1.22] is an enzyme distinct from L-DOPA decarboxylase [L-aromatic amino acid carboxylyase, DDC, EC 4.1.1.28]: the two decarboxylases from fetal rat liver were completely separated from each other by DEAE-cellulose column chromatography and by affinity chromatography with L-carnosine as a ligand.	DEAE-Cellulose	264-278	dopa decarboxylase	Rattus norvegicus	98-118
3933801-3	1985	In addition to their behavior on Sephadex G-50, the immunoactive insulin-related materials from the microbial sources behaved like authentic vertebrate insulins in their ability to be adsorbed to and eluted from disposable octadecasilylsilica cartridges, DEAE-Sephadex, DEAE-cellulose, and one system of high-pressure liquid chromatography (HPLC).	DEAE-Cellulose	270-284	insulin	Homo sapiens	65-72
3876830-1	1985	Chromatofocusing was used to purify the vitamin D-binding protein (DBP) from pig plasma in a procedure that consisted of an initial DEAE-cellulose chromatography followed by DEAE-Sephadex chromatography, with final purification by chromatofocusing.	DEAE-Cellulose	132-146	GC vitamin D binding protein	Sus scrofa	40-65
3876830-1	1985	Chromatofocusing was used to purify the vitamin D-binding protein (DBP) from pig plasma in a procedure that consisted of an initial DEAE-cellulose chromatography followed by DEAE-Sephadex chromatography, with final purification by chromatofocusing.	DEAE-Cellulose	132-146	GC vitamin D binding protein	Sus scrofa	67-70
3922456-5	1985	The IL-3 produced by the COS-1 cells was partially purified using diethylaminoethyl Sephacel and phenyl-Sepharose, and its chromatographic properties were the same as IL-3 produced by the WEHI-3 cell line.	DEAE-Cellulose	66-92	interleukin 3	Mus musculus	4-8
4005291-1	1985	Using a classical methodology of purification consisting of three chromatographic steps (Octyl-Sepharose, DEAE-cellulose, CM-cellulose) we have purified a new cytochrome P-450 from human liver microsomes.	DEAE-Cellulose	106-120	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	159-175
2990549-3	1985	The dTk activity induced by EB virus coelutes from DEAE-cellulose columns with deoxycytidine kinase (dCk) activity and elutes as a broad peak well separated from the large peaks of cellular dTk and dCk activities.	DEAE-Cellulose	51-65	deoxycytidine kinase	Homo sapiens	79-99
3860259-2	1985	M-PST activity was separated and purified from phenol-sulfating activity by anion-exchange chromatography on DEAE-cellulose and subsequently purified on AffiGel Blue and Sephacryl S-200, routinely giving a final purification of over 20 000-fold, with approximately a 3% yield.	DEAE-Cellulose	109-123	mercaptopyruvate sulfurtransferase	Homo sapiens	0-5
2990549-3	1985	The dTk activity induced by EB virus coelutes from DEAE-cellulose columns with deoxycytidine kinase (dCk) activity and elutes as a broad peak well separated from the large peaks of cellular dTk and dCk activities.	DEAE-Cellulose	51-65	Tachykinin	Drosophila melanogaster	4-7
3872125-1	1985	Human peripheral blood leukocyte-derived interleukin-2 (IL-2) was resolved by DEAE-cellulose column chromatography into three peaks of activity, IL-2A, B, and C, with isoelectric points of 7.2, 6.6, and 7.9, respectively.	DEAE-Cellulose	78-92	interleukin 2	Homo sapiens	41-54
3994685-3	1985	or DEAE-cellulose-chromatographic profile of solubilized microsomal preparations from such rats revealed a marked decrease in the cytochrome P-450 content of several eluted fractions compared with that of microsomes from corresponding non-AIA-treated controls.	DEAE-Cellulose	3-17	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	130-146
3872125-1	1985	Human peripheral blood leukocyte-derived interleukin-2 (IL-2) was resolved by DEAE-cellulose column chromatography into three peaks of activity, IL-2A, B, and C, with isoelectric points of 7.2, 6.6, and 7.9, respectively.	DEAE-Cellulose	78-92	interleukin 2	Homo sapiens	56-60
3000845-1	1985	Two isozymes of cytochrome P-450 were partially purified to specific contents of 7.0 and 0.5 nmol/mg of protein, respectively, from placenta of non-smoking women by chromatography on octyl Sepharose, hydroxylapatite, DEAE-cellulose and CM-cellulose.	DEAE-Cellulose	217-231	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	16-32
2858424-8	1985	It was found by DEAE-cellulose thin layer chromatography that the IMP dehydrogenase converted 6-TIMP to 6-thioxanthylic acid (6-TXMP).	DEAE-Cellulose	16-30	tissue inhibitor of metalloproteinase 1	Mus musculus	96-100
3882420-6	1985	This protease and the factor altering ER-DNA binding were eluted together from chromatography on DEAE-cellulose, AcA 44, and carboline-agarose and were sensitive to the same inhibitors.	DEAE-Cellulose	97-111	estrogen receptor 1	Bos taurus	38-40
2578390-3	1985	Human actin-depolymerizing factor (ADF) has been purified by ammonium sulfate fractionation, DEAE-cellulose and blue-Sepharose chromatography.	DEAE-Cellulose	93-107	destrin, actin depolymerizing factor	Homo sapiens	35-38
3880759-4	1985	The immunoreactive myosin polypeptide was purified from the hemolysate to approximately 85% purity by DEAE-cellulose chromatography followed by gel filtration on Sephacryl S-400.	DEAE-Cellulose	102-116	myosin heavy chain 14	Homo sapiens	19-25
4088983-3	1985	Mouse transferrin was prepared from a 50-75% ammonium sulfate fraction of mouse ascites fluid by CM- and DEAE-cellulose chromatography.	DEAE-Cellulose	105-119	transferrin	Mus musculus	6-17
4086199-3	1985	A separation of the albumin- and transferrin-proteins by ion-exchange chromatography using DEAE-cellulose showed the 239Np being entirely bound to the iron-carrier protein transferrin.	DEAE-Cellulose	91-105	transferrin	Rattus norvegicus	33-44
3939542-1	1985	Two forms of prolidase can be separated for all the human cells and tissues examined by DEAE-cellulose column chromatography or batch methods.	DEAE-Cellulose	88-102	peptidase D	Homo sapiens	13-22
6543238-2	1984	The method is based on the adsorption of the 5 alpha-dihydrotestosterone-ABP complex onto DEAE-cellulose filter paper discs at pH 8.5.	DEAE-Cellulose	90-104	sex hormone binding globulin	Homo sapiens	73-76
4086199-3	1985	A separation of the albumin- and transferrin-proteins by ion-exchange chromatography using DEAE-cellulose showed the 239Np being entirely bound to the iron-carrier protein transferrin.	DEAE-Cellulose	91-105	transferrin	Rattus norvegicus	172-183
6238094-7	1984	However, BF and IL 2 were separable during ion exchange chromatography on the DEAE cellulose and phenyl-Sepharose chromatography.	DEAE-Cellulose	78-92	interleukin 2	Homo sapiens	16-20
6210078-1	1984	Three peptide fragments (designated II, III and IV) of human prostatic acid phosphatase (PAP) were isolated to homogeneity from a limited tryptic hydrolysate of PAP by gel filtration on Sephadex G-100, followed by chromatography on DEAE-cellulose and Sephadex G-75.	DEAE-Cellulose	232-246	acid phosphatase 3	Homo sapiens	61-87
6498217-9	1984	The existence of two different forms of ornithine decarboxylase in cardiac tissue was indicated by DEAE-cellulose chromatography.	DEAE-Cellulose	99-113	ornithine decarboxylase 1	Rattus norvegicus	40-63
6093699-1	1984	Ubiquitin was isolated from bovine erythrocytes by a relatively simple procedure involving extraction with chloroform and ethanol, chromatography on DEAE-cellulose, and gel filtration.	DEAE-Cellulose	149-163	ubiquitin	Bos taurus	0-9
6092041-2	1984	By partial purification on DEAE-cellulose columns, it was shown that this protein kinase activity is cAMP independent and that its preferential substrate is casein and not histone.	DEAE-Cellulose	27-41	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	74-88
6545995-1	1984	By the method of precipitation with Rivanol (2-ethoxy-6,9-diaminoacridine lactate) and ammonium sulphate followed by chromatography on DEAE cellulose three genetic variants of transferrin were purified from equine serum: D, M and R. Their molecular mass determined in this study was 80 000, and it was identical for all three variants, which differed slightly in their amino acid composition.	DEAE-Cellulose	135-149	inhibitor of carbonic anhydrase	Equus caballus	176-187
6513553-4	1984	The activating effect of ATP on the glucocorticoid-receptor complexes and sensitivity of this activation to sodium molybdate was also confirmed by DEAE-cellulose chromatography of cytosolic receptor preparations.	DEAE-Cellulose	147-161	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	36-59
6501251-4	1984	Bovine erythrocyte acetylcholinesterase released by PI-specific phospholipase C was purified by column chromatography on DEAE-cellulose, affinity gel and Sepharose 6B, to a homogeneous state, as indicated by polyacrylamide gel electrophoresis, with a recovery of 39%.	DEAE-Cellulose	121-135	acetylcholinesterase	Equus caballus	19-39
6432055-1	1984	Immunochemical characterizations of aldose reductase and aldehyde reductases I and II, partially purified by DEAE-cellulose (DE-52) column chromatography from human tissues, were carried out by immunotitration, using antisera raised against the homogenous preparations of human and bovine lens aldose reductase and human placenta aldehyde reductase I and aldehyde reductase II.	DEAE-Cellulose	109-123	aldo-keto reductase family 1 member B	Homo sapiens	36-52
6432056-5	1984	This tyrosinase fraction was subjected to trypsin (EC 3.4.21.4) cleavage, Sephacryl S-200, hydroxylapatite and DEAE-cellulose chromatography.	DEAE-Cellulose	111-125	tyrosinase	Gallus gallus	5-15
6490752-1	1984	The major forms of cytochrome P-450 in the hepatic microsomes of rats pretreated with phenobarbital (PB) or 3-methylcholanthrene (3MC) were isolated by sequential chromatography on n-octylamino-Sepharose 4B and DEAE-cellulose columns.	DEAE-Cellulose	211-225	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	19-35
6733569-1	1984	An isozyme of S-adenosylmethionine synthetase has been purified to homogeneity by ammonium sulfate fractionation, DEAE-cellulose column chromatography, and gel filtration on a Sephadex G-200 column.	DEAE-Cellulose	114-128	methionine adenosyltransferase 1A	Rattus norvegicus	14-45
6208186-6	1984	PRF was purified from the "lysine-Sepharose eluate" by DEAE-cellulose column chromatography and gel filtration on a Sephadex G-100 column.	DEAE-Cellulose	55-69	Spi-C transcription factor (Spi-1/PU.1 related)	Mus musculus	0-3
6233284-3	1984	The purified actin shares many attributes with numerous other actins that have been characterized, including molecular weight, strong binding to DEAE-cellulose, binding to DNase I, reversible polymerization to F-actin, binding of rabbit myosin subfragment 1 to give distinctive arrowheads , formation of Mg paracrystals, and activation of myosin Mg2+-ATPase.	DEAE-Cellulose	145-159	actin	Oryctolagus cuniculus	13-18
6431749-3	1984	TG was purified by differential salt fractionation and DEAE-cellulose chromatography.	DEAE-Cellulose	55-69	thyroglobulin	Homo sapiens	0-2
6089978-5	1984	Purification of p68 was achieved by passage of a 100 000 X g supernatant fraction over DEAE-cellulose, fractionation with ammonium sulfate, and chromatography on hydroxylapatite.	DEAE-Cellulose	87-101	KH domain containing, RNA binding, signal transduction associated 1	Mus musculus	16-19
6588375-1	1984	At an early purification stage, DNA polymerase alpha holoenzyme from calf thymus can be separated into four different forms by chromatography on DEAE-cellulose.	DEAE-Cellulose	145-159	DNA polymerase alpha 1, catalytic subunit	Homo sapiens	32-52
6088476-1	1984	Basic estrogen receptor (ER) molecule (vero-ER) of the cytosol of porcine uterus was purified 1,200-fold after successive chromatographies on phenyl-Sepharose, hydroxylapatite, and DEAE-cellulose, followed by Sephadex G-150 gel filtration.	DEAE-Cellulose	181-195	estrogen receptor 1	Homo sapiens	6-23
6732781-1	1984	The carboxy terminal fragment of human plasma fibronectin has been isolated after tryptic digestion and separation by DEAE-cellulose chromatography and gel filtration on Sephadex G-50.	DEAE-Cellulose	118-132	fibronectin 1	Homo sapiens	46-57
6204972-1	1984	DNase I in human urine was purified to an electrophoretically homogeneous state by column chromatographies on DEAE-lignocellulose, hydroxyapatite, DEAE-cellulose, Sephadex G-75 and elastin-celite.	DEAE-Cellulose	147-161	deoxyribonuclease 1	Bos taurus	0-7
6323447-1	1984	Vinculin, isolated from turkey gizzard smooth muscle, was purified by chromatography on CM-cellulose after isolation from a DEAE-cellulose column.	DEAE-Cellulose	124-138	vinculin	Meleagris gallopavo	0-8
6199415-3	1984	DEAE-cellulose chromatography separated CHF activity from the majority of interleukin 1 (IL 1), interleukin 2 (IL 2), granulocyte-macrophage colony-stimulating factor (CSF), and interferon (IFN).	DEAE-Cellulose	0-14	interleukin 1 complex	Mus musculus	89-93
6323447-7	1984	The factor(s) in DEAE-cellulose-purified vinculin responsible for decreasing the low shear viscosity of actin was removed and found in a crude fraction isolated by CM-cellulose chromatography.	DEAE-Cellulose	17-31	vinculin	Meleagris gallopavo	41-49
6477130-6	1984	P14 was finally purified by ion exchange chromatography on sulfopropyl (SP-C25) Sephadex and on DEAE cellulose.	DEAE-Cellulose	96-110	pathogenesis-related leaf protein 6	Solanum lycopersicum	0-3
6422856-1	1984	Malonyl-CoA decarboxylase was purified (800-fold) from an erythromycin-producing strain of Streptomyces erythreus using DEAE-cellulose, Sephadex G-100, SP-Sephadex, and gel filtration with Sephadex G-75.	DEAE-Cellulose	120-134	malonyl-CoA decarboxylase	Homo sapiens	0-25
6432425-1	1984	A new method of inhibitor elution from DEAE cellulose is described for carbonic anhydrase III.	DEAE-Cellulose	39-53	carbonic anhydrase 3	Homo sapiens	71-93
6534377-1	1984	A method for the isolation of liver microsomal cytochrome P-450 from phenobarbital-treated rats is described which is based on chromatography on 1-adamantane-carbonyl-aminohexyl-Sepharose 4B, subsequent ion exchange chromatography on DEAE-cellulose and detergent removal by adsorption on silica gel G. The method gives preparations with high electrophoretic homogeneity which correspond to a major phenobarbital-inducible form of rat liver microsomal cytochrome P-450.	DEAE-Cellulose	234-248	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	47-63
6438877-1	1984	A Fab-fragment was obtained from rabbit anti-swine JgG serum through the breakdown of JgG by means of the proteolytic enzyme pepsin in ion-exchange chromatography on DEAE cellulose.	DEAE-Cellulose	166-180	FA complementation group B	Homo sapiens	2-5
6679751-2	1983	Phenylalanine hydroxylase from fresh human liver was purified to homogeneity with a 60% yield by a three steps procedure involving hydrophobic chromatography on Phenyl-Sepharose, ion exchange chromatography on DEAE-Cellulose and High Performance gel permeation chromatography.	DEAE-Cellulose	210-224	phenylalanine hydroxylase	Homo sapiens	0-25
6661223-1	1983	The major form of cytochrome P-450 isolated and purified from the hepatic microsomes of phenobarbital pretreated rats by sequential chromatography on n-octylamino-Sepharose 4B and DEAE-cellulose columns was found to be homogeneous by sodium dodecyl sulphate-polyacrylamide gel electrophoresis.	DEAE-Cellulose	180-194	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	18-34
6659079-1	1983	Calmodulin, a Ca2+-binding protein activator of a series of enzymes, was isolated from the female rabbit myometrium in a homogenous state by DEAE-cellulose chromatography.	DEAE-Cellulose	141-155	calmodulin	Oryctolagus cuniculus	0-10
6641731-1	1983	Three fractions (DE-I, DE-II and DE-III) of Z-protein (fatty acid binding protein) have been isolated from rat liver cytosol by DEAE-cellulose chromatography and characterized.	DEAE-Cellulose	128-142	fatty acid binding protein 1	Rattus norvegicus	44-53
6641731-1	1983	Three fractions (DE-I, DE-II and DE-III) of Z-protein (fatty acid binding protein) have been isolated from rat liver cytosol by DEAE-cellulose chromatography and characterized.	DEAE-Cellulose	128-142	glutamic-oxaloacetic transaminase 2	Rattus norvegicus	55-82
6360438-3	1983	The DEAE-cellulose purified IgG preparations of five additional RA patients stimulated intracellular cathepsin B activity significantly above IgG from healthy controls.	DEAE-Cellulose	4-18	cathepsin B	Homo sapiens	101-112
6654860-2	1983	CRP was strongly adsorbed on a DEAE-cellulose column and was easily separated from other serum proteins.	DEAE-Cellulose	31-45	C-reactive protein	Homo sapiens	0-3
6138099-8	1983	We report here on investigations of plasma fibronectin that had been purified from the "heparin-precipitable fraction" of plasma by DEAE-cellulose chromatography using buffers containing a chaotropic salt (KSCN).	DEAE-Cellulose	132-146	fibronectin 1	Homo sapiens	43-54
6311821-3	1983	Proteins eluted from DEAE-cellulose columns by 0.25 M NaCl contained a collagen species which was resistant to mammalian collagenase and had alpha chains with hydroxylysine/lysine ratios and CNBr peptide patterns similar to alpha 1(V) and alpha 2(V).	DEAE-Cellulose	21-35	collagen type V alpha 1 chain	Homo sapiens	224-234
6311821-3	1983	Proteins eluted from DEAE-cellulose columns by 0.25 M NaCl contained a collagen species which was resistant to mammalian collagenase and had alpha chains with hydroxylysine/lysine ratios and CNBr peptide patterns similar to alpha 1(V) and alpha 2(V).	DEAE-Cellulose	21-35	collagen type V alpha 2 chain	Homo sapiens	239-249
6226459-2	1983	Differential isozyme detection of beta-hexosaminidase in cell free amniotic fluid by DEAE cellulose column chromatography and cellulose acetate paper electrophoresis showed an affected fetus in the first pregnancy and an unaffected in the second.	DEAE-Cellulose	85-99	O-GlcNAcase	Homo sapiens	34-53
6615885-1	1983	Cyclic nucleotide-independent and Ca2+-independent phosvitin kinase was purified from pig testis to apparent homogeneity by DEAE-cellulose, Sephadex G-200 chromatography, followed by subsequent DEAE-cellulose chromatography and phosvitin-Sepharose 4B affinity chromatography.	DEAE-Cellulose	124-138	casein kinase II subunit beta	Sus scrofa	51-60
6419373-3	1983	Human VIII:vWF was purified from a phosphate precipitate of A1(OH)3 absorbed plasma using 4% agarose and DEAE cellulose.	DEAE-Cellulose	105-119	von Willebrand factor	Homo sapiens	11-14
6615885-1	1983	Cyclic nucleotide-independent and Ca2+-independent phosvitin kinase was purified from pig testis to apparent homogeneity by DEAE-cellulose, Sephadex G-200 chromatography, followed by subsequent DEAE-cellulose chromatography and phosvitin-Sepharose 4B affinity chromatography.	DEAE-Cellulose	194-208	casein kinase II subunit beta	Sus scrofa	51-60
6626181-2	1983	Uroporphyrinogen decarboxylase (EC 4.1.1.37) has been purified 4419-fold to a specific activity of 58.3 nmol of coproporphyrinogen III formed/min per mg of protein (with pentacarboxyporphyrinogen III as substrate) from human erythrocytes by adsorption to DEAE-cellulose, (NH4)2SO4 fractionation, gel filtration, phenyl-Sepharose chromatography and polyacrylamide-gel electrophoresis.	DEAE-Cellulose	255-269	uroporphyrinogen decarboxylase	Homo sapiens	0-30
6355549-1	1983	1) Renin-like enzyme of rat aorta was purified by chromatography with DEAE-cellulose and Sephadex G-200.	DEAE-Cellulose	70-84	renin	Rattus norvegicus	3-8
6885823-13	1983	Native phosphorylated P47 was purified from thrombin-stimulated 32P-labeled platelets by ammonium sulfate fractionation and column chromatography on DEAE-cellulose, phenyl-Sepharose, and hydroxylapatite.	DEAE-Cellulose	149-163	pleckstrin	Homo sapiens	22-25
6196237-2	1983	Rabbit anti-human TBG antiserum was precipitated with 50% ammonium sulfate followed by passing a DEAE-cellulose column.	DEAE-Cellulose	97-111	serpin family A member 7	Homo sapiens	18-21
6626221-1	1983	Hexokinase able to bind to mitochondria was purified to homogeneity from rat brain by two successive DEAE-cellulose chromatographic steps.	DEAE-Cellulose	101-115	hexokinase	Saccharomyces cerevisiae S288C	0-10
6626522-1	1983	Uroporphyrinogen decarboxylase (EC 4.1.1.37) has been purified to homogeneity from bovine liver by using isoelectric and salt precipitations, followed by chromatography on DEAE-cellulose, phenyl-Sepharose, hydroxylapatite, and Sephacryl S-200.	DEAE-Cellulose	172-186	uroporphyrinogen decarboxylase	Bos taurus	0-30
6873061-1	1983	We have identified an endogenous regulator of the glucocorticoid receptor following fractionation of dialyzed rat liver cytosol on DEAE-cellulose.	DEAE-Cellulose	131-145	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	50-73
6873061-2	1983	The macromolecular regulator, purified approximately 20-fold as judged by Lowry-reactive material, inhibits activation of glucocorticoid-receptor complexes when assayed by DNA-cellulose binding and by chromatography on DEAE-cellulose minicolumns.	DEAE-Cellulose	219-233	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	122-145
6873061-3	1983	In addition the active DEAE-cellulose fraction stabilizes the unoccupied glucocorticoid receptor against heat inactivation.	DEAE-Cellulose	23-37	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	73-96
6221764-1	1983	An alpha-actinin-like protein was partially purified from the Triton-insoluble cytoskeleton of porcine kidney by 0.6 M MgCl2 treatment, ammonium sulfate fractionation, DEAE-cellulose chromatography and hydroxyapatite chromatography.	DEAE-Cellulose	168-182	actinin, alpha 4	Gallus gallus	3-16
6353206-5	1983	These beta 2m-binding molecules exhibited size- and charge-homogeneity when separated by gel filtration (Sepharose 4B) and by ion-exchange chromatography (DEAE-cellulose), respectively.	DEAE-Cellulose	155-169	beta-2-microglobulin	Homo sapiens	6-13
6134723-1	1983	We have purified a novel membrane ATPase from Streptococcus faecalis by the following procedure: extraction of membranes with Triton X-100 followed by fractionation of the extract by successive DEAE-cellulose chromatography, hydroxylapatite chromatography and Cm-Sepharose chromatography.	DEAE-Cellulose	194-208	ATPase	Enterococcus faecalis	34-40
6192211-1	1983	Angiotensin-converting enzyme was solubilized with papain from a particulate fraction of rat brain and purified to apparent homogeneity by a procedure including DEAE-cellulose, hydroxylapatite, Sephadex G-200, Cys(Bzl)-Pro-Sepharose, and ricin-Sepharose chromatography.	DEAE-Cellulose	161-175	angiotensin I converting enzyme	Rattus norvegicus	0-29
6192143-5	1983	Subsequent chromatography of the apparently homogeneous colonic mucin on DEAE-cellulose revealed the presence of at least six distinct mucin species (mucin I-VI).	DEAE-Cellulose	73-87	LOC100508689	Homo sapiens	64-69
6847673-1	1983	Cytosolic epoxide hydrolase was purified from male Swiss mouse liver cytosol by passing it sequentially through CM-cellulose, DEAE-cellulose, phenylsepharose, DEAE-cellulose, and hydroxyapatite.	DEAE-Cellulose	126-140	epoxide hydrolase 2, cytoplasmic	Mus musculus	0-27
6309758-1	1983	A calcium-activated neutral protease (CANP) was purified from monkey cardiac muscle by a method involving column chromatography on DEAE-cellulose, Sepharose CL-6B, DEAE-Sephacel, organomercurial-Sepharose 4B, and Sephadex G-150 in succession.	DEAE-Cellulose	131-145	calpain 1	Homo sapiens	38-42
6304731-4	1983	The enzyme has been purified from bacteria by extraction with urea and chromatography on DEAE-cellulose and converted to enzymatically active chymosin by acidification and neutralization.	DEAE-Cellulose	89-103	chymosin	Bos taurus	142-150
6339151-2	1983	Inactive renin was isolated from human amniotic fluid by chromatography with DEAE-cellulose, pepstatin-aminobutyl-agarose, octylagarose and Cibacron Blue F3GA columns.	DEAE-Cellulose	77-91	renin	Homo sapiens	9-14
6847673-1	1983	Cytosolic epoxide hydrolase was purified from male Swiss mouse liver cytosol by passing it sequentially through CM-cellulose, DEAE-cellulose, phenylsepharose, DEAE-cellulose, and hydroxyapatite.	DEAE-Cellulose	159-173	epoxide hydrolase 2, cytoplasmic	Mus musculus	0-27
6433926-4	1983	This extracted CRP was further purified by sequential treatment on column chromatography of DEAE cellulose (DE52) and gel filtration using Sephacryl S-300.	DEAE-Cellulose	92-106	C-reactive protein	Homo sapiens	15-18
6300064-3	1983	Fractionation of the extracts by DEAE-cellulose and Sephadex G-150 chromatography yielded a purified actin that would copolymerize with rabbit skeletal muscle actin or polymerize alone into long filaments at 24 degrees C upon addition of 100 mM KC1 and 2 mM MgCl2.	DEAE-Cellulose	33-47	actin	Oryctolagus cuniculus	101-106
6342669-1	1983	Class I isoenzymes of alcohol dehydrogenase (ADH) were isolated by chromatography of human liver homogenates on DEAE-cellulose, 4-[3-[N-(6-aminocaproyl)-amino]propyl]pyrazole--Sepharose and CM-cellulose.	DEAE-Cellulose	112-126	aldo-keto reductase family 1 member A1	Homo sapiens	22-43
6342669-1	1983	Class I isoenzymes of alcohol dehydrogenase (ADH) were isolated by chromatography of human liver homogenates on DEAE-cellulose, 4-[3-[N-(6-aminocaproyl)-amino]propyl]pyrazole--Sepharose and CM-cellulose.	DEAE-Cellulose	112-126	aldo-keto reductase family 1 member A1	Homo sapiens	45-48
6830850-5	1983	The second enzyme activity eluted from DEAE-cellulose at phosphate concentrations higher than 300 mM, phosphorylated only phosvitin and was not retained on phosphocellulose.	DEAE-Cellulose	39-53	casein kinase 2 beta	Homo sapiens	122-131
6402775-2	1983	DNA polymerase alpha has been purified from mitochondria-free crude extracts of the mutant and its parental wild-type cells by sequential column chromatography on DEAE-cellulose and phosphocellulose.	DEAE-Cellulose	163-177	DNA polymerase alpha 1, catalytic subunit	Homo sapiens	0-20
6291759-2	1983	HK III was separated from other known adrenocortical protein kinases by diethylaminoethyl cellulose chromatography.	DEAE-Cellulose	72-99	hexokinase 3	Homo sapiens	0-6
6873037-4	1983	The A2 and B enzymes were separated on DEAE-cellulose.	DEAE-Cellulose	39-53	ATPase H+ transporting V0 subunit a2	Homo sapiens	4-12
16453488-1	1983	Nodulin-35, a protein specific to soybean root nodules, was purified under non-denaturing conditions (DEAE-cellulose followed by Sephacryl S-200 chromatography) to homogeneity.	DEAE-Cellulose	102-116	uricase-2 isozyme 2	Glycine max	0-10
6401186-2	1983	LIP was purified 166-fold from liver extract (LE) by a combination of gel filtration and ion exchange chromatography, using AcA 44, DEAE-cellulose, hydroxylapatite and Sephadex G-150 superfine.	DEAE-Cellulose	132-146	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	Homo sapiens	0-3
27519438-2	1982	Separation of Ca(2+)-stimulated lipoxygenase from lipoxygenase active in the absence of Ca(2+) (lipoxygenase-1) was readily obtained using a DEAE-cellulose column.	DEAE-Cellulose	141-155	linoleate 9S-lipoxygenase-4	Glycine max	32-44
7159606-3	1982	The enzyme acquired by the fibroblasts was shown to be identical to beta-glucuronidase from donor lymphocytes by its position of elution from DEAE-cellulose, thermal stability, mobility on polyacrylamide gels and by its antigenic determinants.	DEAE-Cellulose	142-156	glucuronidase beta	Homo sapiens	68-86
6819292-1	1982	Ornithine aminotransferase [EC 2.6.1.13] was purified and crystallized from human liver by a procedure involving heat treatment, chromatographies on DEAE-cellulose, Octyl-Sepharose CL-4B and Sephadex G-200, and crystallization.	DEAE-Cellulose	149-163	ornithine aminotransferase	Homo sapiens	0-26
6319870-5	1983	Both PDP-2 (enkephalinase) and PDP-3 are apparently present in nerve terminal membranes predominantly as inactive proenzyme precursors, which elute from DEAE-cellulose at high salt concentration, and are activated very slowly by a process involving one or more trypsin-like enzymes.	DEAE-Cellulose	153-167	pyruvate dehydrogenase phosphatase catalytic subunit 2	Rattus norvegicus	5-10
6319870-5	1983	Both PDP-2 (enkephalinase) and PDP-3 are apparently present in nerve terminal membranes predominantly as inactive proenzyme precursors, which elute from DEAE-cellulose at high salt concentration, and are activated very slowly by a process involving one or more trypsin-like enzymes.	DEAE-Cellulose	153-167	membrane metallo-endopeptidase	Rattus norvegicus	12-25
27519438-2	1982	Separation of Ca(2+)-stimulated lipoxygenase from lipoxygenase active in the absence of Ca(2+) (lipoxygenase-1) was readily obtained using a DEAE-cellulose column.	DEAE-Cellulose	141-155	linoleate 9S-lipoxygenase-4	Glycine max	50-62
27519438-2	1982	Separation of Ca(2+)-stimulated lipoxygenase from lipoxygenase active in the absence of Ca(2+) (lipoxygenase-1) was readily obtained using a DEAE-cellulose column.	DEAE-Cellulose	141-155	seed linoleate 13S-lipoxygenase-1	Glycine max	96-110
6816595-2	1982	Human progastricsin was prepared from extracts of gastric mucosa by chromatography on columns of DEAE-cellulose.	DEAE-Cellulose	97-111	progastricsin	Homo sapiens	6-19
6292183-8	1982	These studies also indicated that the cGMP-stimulated phosphodiesterase was immunologically distinct from the other major cGMP-binding proteins present in lung extract and that it could be separated from these binding proteins by chromatography on DEAE-cellulose.	DEAE-Cellulose	248-262	phosphodiesterase 2A	Bos taurus	38-71
6296930-1	1982	Mevalonate kinase from neonatal chick liver has been partially purified by ammonium sulphate precipitation and Sephadex G100 and DEAE-cellulose fractionation.	DEAE-Cellulose	129-143	mevalonate kinase	Gallus gallus	0-17
6128088-1	1982	Tyrosine aminotransferase (EC 2.6.1.5) of human liver was purified 2200-fold by successive chromatography on DEAE-cellulose DE-52, Ultrogel AcA-34, CM-Sephadex C-50 and hydroxyapatite to a specific activity of 64 units/mg of protein.	DEAE-Cellulose	109-123	tyrosine aminotransferase	Homo sapiens	0-25
6809821-3	1982	The results demonstrate that the factor required for growth of these cell lines copurifies with IL 3 activity on G-100, DEAE cellulose, and CM cellulose column chromatography as well as in preparative isoelectric focusing and on hydrophobic supports in reverse phase high pressure liquid chromatography.	DEAE-Cellulose	120-134	interleukin 3	Mus musculus	96-100
7140762-3	1982	In the second step, ion-exchange chromatography through a DEAE-cellulose column, progesterone receptor was eluted as a single peak at 0.1 M KCl.	DEAE-Cellulose	58-72	progesterone receptor	Gallus gallus	81-102
7174639-1	1982	An aminopeptidase was purified about 700-fold from porcine liver homogenate by ammonium sulfate fractionation and a series of column chromatographies on DEAE-cellulose, Sephadex G-150, DEAE-Sepharose, and hydroxyapatite.	DEAE-Cellulose	153-167	carboxypeptidase Q	Homo sapiens	3-17
6809749-2	1982	The "major" phenobarbital (PB)-induced cytochrome P-450 species present in livers of male Sprague-Dawley rats was resolved into two catalytically active heme-protein fractions on diethylaminoethyl cellulose.	DEAE-Cellulose	179-206	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	39-55
6752022-5	1982	The peak 1 fraction was adsorbed onto DEAE-cellulose and eluted by a linear gradient of NaCl.	DEAE-Cellulose	38-52	inactive tyrosine-protein kinase PEAK1	Meleagris gallopavo	4-10
6288486-2	1982	The angiotensin I-converting enzyme in normal human urine was partially purified with ammonium surfate (3.2M), DEAE-Cellulose ion exchange chromatography (0-0.5M NaCl gradient), and Sephadex G 200 gel filtration.	DEAE-Cellulose	111-125	angiotensin I converting enzyme	Homo sapiens	4-35
6215059-2	1982	The protein, SAIP (for serum actin inhibitory protein), has been purified by affinity chromatography of serum over actin-Sepharose followed by protein fractionation with ammonium sulfate and chromatography over DEAE-cellulose.	DEAE-Cellulose	211-225	actin	Oryctolagus cuniculus	29-34
6980256-1	1982	Interleukin 2 (IL-2), produced with and without co-stimulation by the Burkitt"s lymphoma line Daudi, was purified 37,000-fold to apparent homogeneity from lymphocyte conditioned medium by (NH4)2SO4 precipitation, DEAE-cellulose ion-exchange chromatography, gel filtration, and chromatography on blue agarose and on Procion-red agarose.	DEAE-Cellulose	213-227	interleukin 2	Homo sapiens	0-13
6981429-1	1982	A new purification method for C1-esterase inhibitor is described, which is essentially a three-step procedure: precipitation with poly(ethylene glycol), chromatography on DEAE-cellulose and hydrophobic interaction chromatography on hexyl-Sepharose.	DEAE-Cellulose	171-185	complement C1s	Homo sapiens	30-41
7082864-1	1982	Red blood cell lysates were applied to DEAE cellulose paper for detection of glucose-6-phosphate dehydrogenase.	DEAE-Cellulose	39-53	glucose-6-phosphate dehydrogenase	Homo sapiens	77-110
7082864-2	1982	Glucose-6-phosphate dehydrogenase (G-6-PD) was separated from 6-phosphogluconate dehydrogenase (6-PGD) by DEAE-cellulose paper-chromatography and their activities were detected on the chromatogram by applying the reaction mixture.	DEAE-Cellulose	106-120	glucose-6-phosphate dehydrogenase	Homo sapiens	0-33
7082864-2	1982	Glucose-6-phosphate dehydrogenase (G-6-PD) was separated from 6-phosphogluconate dehydrogenase (6-PGD) by DEAE-cellulose paper-chromatography and their activities were detected on the chromatogram by applying the reaction mixture.	DEAE-Cellulose	106-120	glucose-6-phosphate dehydrogenase	Homo sapiens	35-41
7082864-2	1982	Glucose-6-phosphate dehydrogenase (G-6-PD) was separated from 6-phosphogluconate dehydrogenase (6-PGD) by DEAE-cellulose paper-chromatography and their activities were detected on the chromatogram by applying the reaction mixture.	DEAE-Cellulose	106-120	phosphogluconate dehydrogenase	Homo sapiens	62-94
7082864-2	1982	Glucose-6-phosphate dehydrogenase (G-6-PD) was separated from 6-phosphogluconate dehydrogenase (6-PGD) by DEAE-cellulose paper-chromatography and their activities were detected on the chromatogram by applying the reaction mixture.	DEAE-Cellulose	106-120	phosphogluconate dehydrogenase	Homo sapiens	96-101
7135497-2	1982	The glutathione reductase from human and dog adrenal cortex was purified by means of precipitation with (NH4)2SO4, by affinity chromatography, sephadex G25, DEAE-cellulose and CM-cellulose chromatography.	DEAE-Cellulose	157-171	glutathione-disulfide reductase	Homo sapiens	4-25
7050099-1	1982	The chloroplast leucyl-tRNA synthetase from Phaseolus vulgaris was purified by ammonium sulfate precipitation and chromatography on DEAE-cellulose, hydroxylapatite, and phosphocellulose.	DEAE-Cellulose	132-146	leucine--tRNA ligase, cytoplasmic	Oryctolagus cuniculus	16-38
6178768-3	1982	Plasma histamine concentrations were measured with a novel double-isotope radiometric assay, and NCF was identified by its elution in the void volume fractions of Sephadex G-200 and as a single peak of activity at approximately 0.20 molar NaCl after anion exchange chromatography on diethylaminoethyl-Sephacel (pH 7.8).	DEAE-Cellulose	283-309	neutrophil cytosolic factor 4	Homo sapiens	97-100
16662494-5	1982	The two isoenzymes of glutamine synthetase have been separated by DEAE-cellulose column chromatography of extracts from the green cotyledons.	DEAE-Cellulose	66-80	glutamate-ammonia ligase	Homo sapiens	22-42
6285697-2	1982	Alpha-galactosidase A was purified from human placenta by chromatography on concanavalin A-Sepharose, DEAE-cellulose, and N-epsilon-aminocaproyl-alpha-D-galactosylamine-Sepharose.	DEAE-Cellulose	102-116	galactosidase alpha	Homo sapiens	0-21
7173815-6	1982	Rat BLP has been purified from liver by a combination of ammonium sulfate fractionation, DEAE-cellulose column chromatography and affinity chromatography using the IgG fraction of rabbit anti-rat BLP serum.	DEAE-Cellulose	89-103	dynein light chain roadblock-type 1	Rattus norvegicus	4-7
7129004-4	1982	Using the 3T3 cell line for assay of activity, the growth factor was partially purified from AH-130 tumor cells by ammonium sulfate fractionation, DEAE-cellulose column chromatography and gel filtration on a Sephacryl S-300 column.	DEAE-Cellulose	147-161	myotrophin	Rattus norvegicus	51-64
6802850-2	1982	Five forms of cytochrome P-450 have been purified from liver microsomes of beta-naphthoflavone-pretreated rats by chromatography on DEAE-Sephadex, DEAE-cellulose, and hydroxylapatite or CM-Sepharose columns.	DEAE-Cellulose	147-161	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	14-30
6896660-1	1982	A DNA-binding protein was partially purified from extracts of HeLa cells by high-speed centrifugation and chromatography on DEAE-cellulose, phosphocellulose and ultraviolet light-irradiated DNA-cellulose columns.	DEAE-Cellulose	124-138	zinc finger protein 763	Homo sapiens	2-21
6281387-1	1982	Acid sphingomyelinase (sphingomyelin phosphodiesterase, EC 3.1.4.12) was purified from human brain by extraction with 0.1% Triton X-100, followed by sequential chromatography on Concanavalin A-Sepharose, octyl-Sepharose, hydroxylapatite, DEAE-cellulose, red A-agarose, Sephadex G-200, and DEAE-cellulose with ampholyte elution.	DEAE-Cellulose	238-252	sphingomyelin phosphodiesterase 1	Homo sapiens	0-21
6281387-1	1982	Acid sphingomyelinase (sphingomyelin phosphodiesterase, EC 3.1.4.12) was purified from human brain by extraction with 0.1% Triton X-100, followed by sequential chromatography on Concanavalin A-Sepharose, octyl-Sepharose, hydroxylapatite, DEAE-cellulose, red A-agarose, Sephadex G-200, and DEAE-cellulose with ampholyte elution.	DEAE-Cellulose	238-252	sphingomyelin phosphodiesterase 1	Homo sapiens	23-54
6281387-1	1982	Acid sphingomyelinase (sphingomyelin phosphodiesterase, EC 3.1.4.12) was purified from human brain by extraction with 0.1% Triton X-100, followed by sequential chromatography on Concanavalin A-Sepharose, octyl-Sepharose, hydroxylapatite, DEAE-cellulose, red A-agarose, Sephadex G-200, and DEAE-cellulose with ampholyte elution.	DEAE-Cellulose	289-303	sphingomyelin phosphodiesterase 1	Homo sapiens	0-21
6281387-1	1982	Acid sphingomyelinase (sphingomyelin phosphodiesterase, EC 3.1.4.12) was purified from human brain by extraction with 0.1% Triton X-100, followed by sequential chromatography on Concanavalin A-Sepharose, octyl-Sepharose, hydroxylapatite, DEAE-cellulose, red A-agarose, Sephadex G-200, and DEAE-cellulose with ampholyte elution.	DEAE-Cellulose	289-303	sphingomyelin phosphodiesterase 1	Homo sapiens	23-54
6802850-3	1982	Over 50% of the starting cytochrome P-450 content can be accounted for in these five forms after resolution on the DEAE-cellulose column, and after further purification, the combined total recovery is 30%.	DEAE-Cellulose	115-129	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	25-41
6801137-5	1982	Serum CRP fails to adsorb to DEAE-cellulose but does adsorb to CM-cellulose, from which it elutes as gamma-mobility antigen.	DEAE-Cellulose	29-43	C-reactive protein	Oryctolagus cuniculus	6-9
6280480-3	1982	The elution profile of angiotensin I-converting enzyme on DEAE cellulose and after gel filtration on Sepharose 4B was unchanged by captopril.	DEAE-Cellulose	58-72	angiotensin I converting enzyme	Rattus norvegicus	23-54
6821160-6	1982	Lactoferrin and serum albumin coeluting as a single peak, were separated by a further chromatography on DEAE-cellulose.	DEAE-Cellulose	104-118	albumin	Homo sapiens	16-29
6801123-11	1982	Protein p28 was eluted from DEAE-cellulose (Whatman DE-52) ion exchange columns at 0.05 to 0.15 M NaCl.	DEAE-Cellulose	28-42	golgi SNAP receptor complex member 1	Homo sapiens	8-11
6459154-6	1982	DEAE-cellulose chromatography was used to resolve the isoenzyme of beta-hexosaminidase.	DEAE-Cellulose	0-14	O-GlcNAcase	Homo sapiens	67-86
7056710-1	1982	Fibrinogen isolated from normal human single donor or pool plasma was fractionated by DEAE-cellulose chromatography.	DEAE-Cellulose	86-100	fibrinogen beta chain	Homo sapiens	0-10
7039698-1	1982	Using a previously developed procedure, further optimization of isolation of the functionally active pigment-protein lipid complex of the reaction center of photosystem 2 (PPLC RC PS-2) by DEAE-cellulose chromatography has been carried out.	DEAE-Cellulose	189-203	taste 2 receptor member 64 pseudogene	Homo sapiens	180-184
6279172-1	1982	A protein kinase activity with high specificity for histone H1 was isolated from mouse plasmacytoma, Morris hepatoma and normal mouse liver and compared by ion exchange chromatography after DEAE-cellulose, hydroxylapatite and Sephadex G-200 chromatography.	DEAE-Cellulose	190-204	H1.2 linker histone, cluster member	Mus musculus	52-62
7067077-6	1982	The PBG-S deficiency was confirmed after DEAE cellulose chromatography: the concordance of relative and specific activity before and after chromatography of PBG-S from patients and controls differs from the findings in lead poisoning.	DEAE-Cellulose	41-55	aminolevulinate dehydratase	Homo sapiens	4-9
6269846-1	1981	A protein kinase with high specificity for histone H1 was purified from a plasmacytoma microsomal fraction by a high-salt wash, ammonium sulfate precipitation, chromatography on DEAE-cellulose, hydroxyapatite and Sephadex G-200 columns, and the main properties of this kinase were studied.	DEAE-Cellulose	178-192	H1.0 linker histone	Mus musculus	43-53
6978269-2	1982	Equine alpha 1-antitrypsin was isolated from horse plasma by a combination of ammonium sulfate and acidification precipitation followed by ion-exchange chromatography on DEAE-cellulose, molecular sieve chromatography on Sephadex G-200 and affinity chromatography on Cibacron Blue-agarose.	DEAE-Cellulose	170-184	alpha-1-antiproteinase 2	Equus caballus	7-26
7198668-1	1982	A tissue plasminogen activator was extracted from skin lesions with allergic vasculitis and purified by successive column chromatography on Sephadex G-200, DEAE-cellulose, Hydroxyaptite-cellulose and polyacrylamide gel electrophoresis.	DEAE-Cellulose	156-170	chromosome 20 open reading frame 181	Homo sapiens	2-30
20487909-1	1982	The breakdown of cytoplasmic tubulin from brain (purified by ammonium sulfate fractionation and DEAE cellulose chromatography) by cathepsin D from brain (purified by ammonium sulfate fractionation and pepstatin Sepharose chromatography) was studied; changes in the intensity of tubulin gel bands were determined.	DEAE-Cellulose	96-110	cathepsin D	Homo sapiens	130-141
6279576-1	1981	Angiotensin converting enzyme [EC 3.4.15.1] was solubilized from the membrane fraction of human kidney cortex using trypsin and purified to homogeneity by DEAE-cellulose, hydroxylapatite and DEAE-Sephadex A-50 column chromatographies, preparative isoelectric focusing, and Sephadex G-200 gel filtration.	DEAE-Cellulose	155-169	angiotensin I converting enzyme	Homo sapiens	0-29
7295788-5	1981	These factors were separated into two less active components (peaks 1 and 2) by DEAE-cellulose chromatography.	DEAE-Cellulose	80-94	pseudopodium-enriched atypical kinase 1	Rattus norvegicus	62-75
7340823-10	1981	Acetonitrile (20%, v/v) was also included in all buffers for DEAE-cellulose chromatography, increasing the resolution and recovery of human prolactin, apparently by minimizing non-ionic interactions with the matrix.	DEAE-Cellulose	61-75	prolactin	Homo sapiens	140-149
6796412-3	1981	Cytochrome P-450 was prepared from the liver microsomes of cholestyramine-fed rats by solubilisation with the non-ionic detergent Nonidet P42 followed by chromatography on a DEAE-cellulose column and on hydroxyapatite.	DEAE-Cellulose	174-188	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	0-16
7021559-1	1981	Human placenta insulin receptor was purified 11,000-fold to near homogeneity using DEAE-cellulose chromatography and affinity chromatography on insulin-Sepharose.	DEAE-Cellulose	83-97	insulin receptor	Homo sapiens	15-31
6794653-1	1981	beta-Galactosidase from Alternaria tenius was purified to homogeneity from the cultural fluid using acetone precipitation, ion-exchange chromatography on DEAE-cellulose, adsorption on hydroxylapatite and affinity chromatography on N-(beta-D-galactopyranosyl-thiocarbamoyl)-beta-aminocaproyl-AN-Sepharose 4B.	DEAE-Cellulose	154-168	CC77DRAFT_1020447	Alternaria alternata	0-18
6788848-4	1981	Although optimal conditions for the production of MCGF in CM are identical to those for the production of T cell growth factor (TCGF), MCGF can be dissociated from TCGF after the first stage of purification on a DEAE-cellulose column.	DEAE-Cellulose	212-226	interleukin 3	Mus musculus	135-139
6114859-1	1981	A soluble, sodium-nitroprusside-stimulated guanylate cyclase as been purified from bovine lung by DEAE-cellulose chromatography, ammonium sulfate precipitation, chromatography on Blue Sepharose CL-6B and preparative gel electrophoresis.	DEAE-Cellulose	98-112	guanylate cyclase	Bos taurus	43-60
6164401-1	1981	Rat alpha 2-macroglobulin was isolated and purified from the pooled sera of turpentine-injected rats by sequential use of dextran sulphate, DEAE-cellulose and gel filtration chromatography.	DEAE-Cellulose	140-154	alpha-2-macroglobulin	Rattus norvegicus	4-25
6263522-10	1981	(4) Transferase and galactokinase activity in human liver is resolved into two major components on DEAE-cellulose columns.	DEAE-Cellulose	99-113	galactokinase 1	Homo sapiens	20-33
7232334-12	1981	Bands representing mobilities of albumin, transferrin and alkaline phosphatase were observed in DEAE-cellulose fractions; however, 12 components of unknown structure were revealed.	DEAE-Cellulose	96-110	transferrin	Homo sapiens	42-53
7305955-1	1981	Two isoenzyme of beta-glucuronidase from a rat basophil leukaemia tumour were co-purified 4067-fold by (NH4)2SO4 precipitation and sequential chromatography on concanavalin A--Sepharose, Sephadex G-200, DEAE-cellulose, CM-cellulose and phosphocellulose.	DEAE-Cellulose	203-217	glucuronidase, beta	Rattus norvegicus	17-35
6453626-1	1981	Some properties of three interconvertible forms of rabbit muscle phosphofructokinase specifically eluted from DEAE-cellulose with 19 mM citrate in 0.1 M tris-phosphate buffer, pH 8,0 (I), with 0,3 M buffer (II) and 1.5 M NaCl (III) are compared.	DEAE-Cellulose	110-124	ATP-dependent 6-phosphofructokinase, muscle type	Oryctolagus cuniculus	65-84
6261905-7	1981	The presence of calmodulin and an inhibitor substance was confirmed by DEAE-cellulose column chromatography.	DEAE-Cellulose	71-85	calmodulin 1	Rattus norvegicus	16-26
7460846-1	1981	PRL secreted by hamster anterior pituitaries was purified by gel filtration on Sephadex G-100 and ion exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	129-143	prolactin	Mus musculus	0-3
7460846-2	1981	Hamster PRL eluted from Sephadex G-100 with an elution volume to void volume ratio of 1.85 and at a salt concentration of 0.13 M NaCl on DEAE-cellulose.	DEAE-Cellulose	137-151	prolactin	Mus musculus	8-11
6778876-2	1981	NADPH-ferredoxin reductase and ferredoxin activities have been identified in bovine thyroid particulate fractions (mainly mitochondria) after ultrasonication and DEAE-cellulose chromatography.	DEAE-Cellulose	162-176	ferredoxin reductase	Bos taurus	6-26
6972868-1	1981	Prolactin was purified from bullfrog adenohypophyses by extraction of acetone-dried powder with acid acetone and chromatography on DEAE-cellulose and Sephadex G100.	DEAE-Cellulose	131-145	prolactin	Homo sapiens	0-9
7240127-6	1981	Like DNA polymerase beta, it sedimented at 3.8S, was resistant to reagents blocking sulfhydryl groups, and was inhibited by phosphate, but it differed from DNA polymerase beta with respect to elution positions from DEAE-cellulose, phosphocellulose and DNA-cellulose columns, Km value (lower by one order of magnitude for dTTP), and template-primer preference.	DEAE-Cellulose	215-229	DNA polymerase beta	Rattus norvegicus	5-24
6113625-1	1981	Gamma-glutamyltranspeptidase (GGT) of adult rat liver was solubilized by treatment with papain and further purified by affinity column chromatography on concanavalin-A Sepharose 4B, followed by ion exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	225-239	gamma-glutamyltransferase 1	Rattus norvegicus	0-28
6113625-1	1981	Gamma-glutamyltranspeptidase (GGT) of adult rat liver was solubilized by treatment with papain and further purified by affinity column chromatography on concanavalin-A Sepharose 4B, followed by ion exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	225-239	gamma-glutamyltransferase 1	Rattus norvegicus	30-33
6113625-2	1981	During DEAE-cellulose chromatography, liver GGT was adsorbed at 0.1M Tris-HCl buffer (pH8.0).	DEAE-Cellulose	7-21	gamma-glutamyltransferase 1	Rattus norvegicus	44-47
7262815-5	1981	Since the enzyme activity is markedly stimulated by phosphatidyl choline or catalase in the enzyme system obtained by DEAE-cellulose chromatography, it is presumed that the enzyme activity is markedly reduced because of removing the H2O2-scavenging system as well as the lipids, which are necessary to activate or stabilize the enzyme, from the microsomal enzyme system.	DEAE-Cellulose	118-132	catalase	Rattus norvegicus	76-84
6113958-2	1981	Arylsulfatase-A and -B activities were assayed in leukocyte extracts following separation of the enzymes by batch chromatography on DEAE cellulose.	DEAE-Cellulose	132-146	arylsulfatase A	Homo sapiens	0-22
7262818-7	1981	Terminal "delta 6-desaturase" was purified from rat liver microsomes for the first time by Triton X-100 solubilization, DEAE-cellulose, CM-Sephadex and cytochrome b5-Sepharose chromatography using its high affinity for cytochrome b5.	DEAE-Cellulose	120-134	fatty acid desaturase 2	Rattus norvegicus	10-28
6789499-4	1980	The hemoglobin fraction eluted with the second eluant was applied onto a DEAE-cellulose column and eluted with 0.2 M glycine containing 0.01 percent KCN, resulting in complete isolation of CA-C at high recovery rate.	DEAE-Cellulose	73-87	carbonic anhydrase 2	Homo sapiens	189-193
7287003-1	1981	Deficient porphobilinogen-synthase (PBG-S) of a previously reported patient with PBG-S defect porphyria (red cell PBG-S activity approximately 2% of the physiological level) has been characterized in erythrocytes after DEAE cellulose chromatography, ultrafiltration and polyacrylamide gel electrophoresis: Residual specific activity of 2.5%, increase of Km, but identical fractionation, concentration and electrophoretic mobility of the enzyme protein compared to controls.	DEAE-Cellulose	219-233	aminolevulinate dehydratase	Homo sapiens	10-34
7287003-1	1981	Deficient porphobilinogen-synthase (PBG-S) of a previously reported patient with PBG-S defect porphyria (red cell PBG-S activity approximately 2% of the physiological level) has been characterized in erythrocytes after DEAE cellulose chromatography, ultrafiltration and polyacrylamide gel electrophoresis: Residual specific activity of 2.5%, increase of Km, but identical fractionation, concentration and electrophoretic mobility of the enzyme protein compared to controls.	DEAE-Cellulose	219-233	aminolevulinate dehydratase	Homo sapiens	36-41
7287003-1	1981	Deficient porphobilinogen-synthase (PBG-S) of a previously reported patient with PBG-S defect porphyria (red cell PBG-S activity approximately 2% of the physiological level) has been characterized in erythrocytes after DEAE cellulose chromatography, ultrafiltration and polyacrylamide gel electrophoresis: Residual specific activity of 2.5%, increase of Km, but identical fractionation, concentration and electrophoretic mobility of the enzyme protein compared to controls.	DEAE-Cellulose	219-233	aminolevulinate dehydratase	Homo sapiens	81-86
6283489-10	1981	After solubilization of membrane-bound enzymes by Triton X-100 followed by chromatography on DEAE cellulose, five peaks of CCK-4 degrading activity were detected (two minor and three major peaks).	DEAE-Cellulose	93-107	protein tyrosine kinase 7 (inactive)	Homo sapiens	123-128
6254970-11	1980	In the most highly purified LDL receptor preparation, which had been subjected to the sequential steps of solubilization, DEAE-cellulose chromatography, agarose gel filtration, and phosphatidylcholine/acetone precipitation, the receptor was estimated to constitute about 5% of the total protein.	DEAE-Cellulose	122-136	low density lipoprotein receptor	Bos taurus	28-40
6159919-1	1980	Serum and amniotic fluid samples from five pregnant women were analyzed for different proteinase inhibitors by ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	142-156	endogenous retrovirus group K member 8, envelope	Homo sapiens	86-96
6253285-8	1980	Moreover, calmodulin-activated phosphodiesterase could be directly demonstrated in cell sonicates subjected to DEAE-cellulose chromatography.	DEAE-Cellulose	111-125	calmodulin	Bos taurus	10-20
7440713-2	1980	ApoE was purified from the very low density lipoproteins of hypertriglyceridemic patients by heparin-agarose affinity chromatography, DEAE-cellulose chromatography, and preparative polyacrylamide gel electrophoresis.	DEAE-Cellulose	134-148	apolipoprotein E	Homo sapiens	0-4
7329823-1	1981	The heptadecapeptide form of rat gastrin was purified by a combination of DEAE cellulose, Sephadex G50 affinity, and high performance liquid chromatography.	DEAE-Cellulose	74-88	gastrin	Rattus norvegicus	33-40
6259062-1	1980	Three different, calmodulin-dependent, isoenzymes of cyclic nucleotide phosphodiesterase (PDE) can be isolated by DEAE cellulose chromatography from the immature rat testis and shown to have different substrate specificities and kinetic behaviour.	DEAE-Cellulose	114-128	calmodulin 1	Rattus norvegicus	17-27
6777221-1	1980	Insulin-degrading enzyme (IDE), which proteolytically degraded insulin with a high degree of specificity, was purified from pig skeletal muscle by ammonium sulfate precipitation, chromatography on Bio-Gel P-200 and DEAE-cellulose, and finally rechromatography on Sephadex G-200 (rechromatography fraction).	DEAE-Cellulose	215-229	insulin degrading enzyme	Sus scrofa	0-24
7459381-2	1980	High molecular weight water-soluble mucin was separated from low molecular weight proteins by gel exclusion chromatography on Sepharose 4B, and was further separated into two major mucin fractions and several non-mucin fractions on DEAE-cellulose.	DEAE-Cellulose	232-246	solute carrier family 13 member 2	Rattus norvegicus	36-41
6165352-1	1980	Cathepsin H was purified from human liver by a method involving autolysis and acetone fractionation, and chromatography on DEAE-cellulose, Ultrogel AcA 54, hydroxyapatite and concanavalin A-Sepharose.	DEAE-Cellulose	123-137	cathepsin H	Homo sapiens	0-11
6932280-1	1980	20 alpha-hydroxysteroid dehydrogenase was found in the supernatant after hemolysis of human erythrocytes, and the enzyme was isolated from the membrane-free hemolysate on a DEAE-cellulose column.	DEAE-Cellulose	173-187	hydroxysteroid 17-beta dehydrogenase 2	Homo sapiens	0-37
6777221-1	1980	Insulin-degrading enzyme (IDE), which proteolytically degraded insulin with a high degree of specificity, was purified from pig skeletal muscle by ammonium sulfate precipitation, chromatography on Bio-Gel P-200 and DEAE-cellulose, and finally rechromatography on Sephadex G-200 (rechromatography fraction).	DEAE-Cellulose	215-229	insulin degrading enzyme	Sus scrofa	26-29
7452289-1	1980	A DEAE-cellulose filter assay for colchicine binding protein (CBP) has been modified to include 1 M-sucrose in the incubation medium (single-point assay).	DEAE-Cellulose	2-16	CREB binding protein	Mus musculus	34-60
7451402-1	1980	An aminopeptidase B from porcine liver was purified about 2,000-fold by ammonium sulfate fractionation and a series of chromatographies on hydroxyapatite, DEAE-cellulose, Sephadex G-150, hydroxyapatite and DEAE-Sepharose columns.	DEAE-Cellulose	155-169	arginyl aminopeptidase	Homo sapiens	3-19
7452289-1	1980	A DEAE-cellulose filter assay for colchicine binding protein (CBP) has been modified to include 1 M-sucrose in the incubation medium (single-point assay).	DEAE-Cellulose	2-16	CREB binding protein	Mus musculus	62-65
6249394-3	1980	However, it was possible to readily demonstrate the presence of a cyclic nucleotide phosphodiesterase activity regulated by calmodulin if the extracts were first purified by batch ion-exchange chromatography over DEAE-cellulose followed by affinity chromatography with calmodulin coupled to Sepharose.	DEAE-Cellulose	213-227	calmodulin 1	Rattus norvegicus	124-134
6773954-4	1980	The enzyme responsible for calmodulin methylation and its substrate, the putative desmethylcalmodulin, were separated from one another by chromatography on DEAE-cellulose.	DEAE-Cellulose	156-170	calmodulin 1	Rattus norvegicus	27-37
6774048-6	1980	The two major SAA polymorphs, designated SAA4 and SAA5 according to their order of elution from DEAE-cellulose, had different NH2-terminal sequences.	DEAE-Cellulose	96-110	serum amyloid A4, constitutive	Homo sapiens	41-45
6933547-1	1980	Two types of normal human plasma fibrinogen--peak 1 and peak 2--are distinquishable by DEAE-cellulose gradient elution chromatography.	DEAE-Cellulose	87-101	fibrinogen beta chain	Homo sapiens	33-43
6933547-1	1980	Two types of normal human plasma fibrinogen--peak 1 and peak 2--are distinquishable by DEAE-cellulose gradient elution chromatography.	DEAE-Cellulose	87-101	pseudopodium enriched atypical kinase 1	Homo sapiens	45-51
6933547-1	1980	Two types of normal human plasma fibrinogen--peak 1 and peak 2--are distinquishable by DEAE-cellulose gradient elution chromatography.	DEAE-Cellulose	87-101	PEAK1 related, kinase-activating pseudokinase 1	Homo sapiens	56-62
7426668-2	1980	Hexokinase D has been purified about 50-fold from the liver of rainbow trout by chromatography with DEAE-cellulose and Sephadex G-200, and by isoelectric focusing.	DEAE-Cellulose	100-114	hexokinase 1	Homo sapiens	0-10
6249394-5	1980	Thus, by employing an initial chromatography step over DEAE-cellulose to separate phosphodiesterase activity from calmodulin, it was possible to increase the recovery of calmodulin-sensitive phosphodiesterase after affinity chromatrography with calmodulin coupled to Sepharose.	DEAE-Cellulose	55-69	calmodulin 1	Rattus norvegicus	114-124
6249394-5	1980	Thus, by employing an initial chromatography step over DEAE-cellulose to separate phosphodiesterase activity from calmodulin, it was possible to increase the recovery of calmodulin-sensitive phosphodiesterase after affinity chromatrography with calmodulin coupled to Sepharose.	DEAE-Cellulose	55-69	calmodulin 1	Rattus norvegicus	170-180
6249394-5	1980	Thus, by employing an initial chromatography step over DEAE-cellulose to separate phosphodiesterase activity from calmodulin, it was possible to increase the recovery of calmodulin-sensitive phosphodiesterase after affinity chromatrography with calmodulin coupled to Sepharose.	DEAE-Cellulose	55-69	calmodulin 1	Rattus norvegicus	170-180
7403570-1	1980	Three types of 15-hydroxyprostaglandin dehydrogenase were identified in rabbit whole kidney homogenate when the centrifuged homogenate was sequentially fractionated by ammonium sulfate precipitation, DEAE-cellulose and Matrex Gel Blue A chromatographies, and Sephadex gel filtration.	DEAE-Cellulose	200-214	carbonyl reductase [NADPH] 1	Oryctolagus cuniculus	15-52
6452177-1	1980	The sedimentation behaviour of the subform of rabbit muscle phosphofructokinase specifically eluted from DEAE cellulose by citrate was studied in different media by velocity experiments.	DEAE-Cellulose	105-119	ATP-dependent 6-phosphofructokinase, muscle type	Oryctolagus cuniculus	60-79
7403570-6	1980	A third type of 15-hydroxyprostaglandin dehydrogenase is also adsorbed to DEAE-cellulose but is partially separable from the other peak 2 enzymes on Matrex Gel Blue A and differs from those enzymes in preferentially oxidizing PGI2.	DEAE-Cellulose	74-88	carbonyl reductase [NADPH] 1	Oryctolagus cuniculus	16-53
6770674-1	1980	Both the common and a variant isozyme of acid alpha-glucosidase have been purified from a heterozygous placenta with CM-Sephadex, ammonium sulfate precipitation, dialysis, Amicon filtration, affinity chromatography by Sephadex G-100, and DEAE-cellulose chromatography.	DEAE-Cellulose	238-252	sucrase-isomaltase	Homo sapiens	46-63
6930304-3	1980	This enzyme after purification by successive column chromatography on DEAE-cellulose, phosphocellulose and hydroxyapatite, was found to have biochemical properties similar to those reported for terminal transferase from calf thymus and human leukemic cells.	DEAE-Cellulose	70-84	DNA nucleotidylexotransferase	Bos taurus	194-214
6104657-3	1980	Papain solubilized gamma-glutamyltranspeptidase was purified by DEAE-cellulose column chromatography.	DEAE-Cellulose	64-78	gamma-glutamyltransferase 1	Rattus norvegicus	19-47
6247353-1	1980	Calmodulin-dependent cyclic nucleotide phosphodiesterase was purified from bovine brain to apparent homogeneity by a new procedure involving DEAE-cellulose, Affi-Gel blue, calmodulin-Sepharose 4B, and Sephadex G-200 column chromatographies.	DEAE-Cellulose	141-155	calmodulin	Bos taurus	0-10
6769729-3	1980	Aldose reductase (AR) was purified from rat and bovine seminal vesicles using DEAE-cellulose, hydroxylapatite, and Sephadex-gel column chromatography.	DEAE-Cellulose	78-92	aldo-keto reductase family 1 member B1	Rattus norvegicus	0-16
6769729-3	1980	Aldose reductase (AR) was purified from rat and bovine seminal vesicles using DEAE-cellulose, hydroxylapatite, and Sephadex-gel column chromatography.	DEAE-Cellulose	78-92	aldo-keto reductase family 1 member B1	Rattus norvegicus	18-20
7370308-3	1980	Uterine thymidine kinase activity was separated into three peaks (peak 1, 2 and 3) by means of DEAE-cellulose column chromatography.	DEAE-Cellulose	95-109	pseudopodium-enriched atypical kinase 1	Rattus norvegicus	66-81
7390973-1	1980	A phospholipase A2 bound tightly to the particulate fractions of rat ascites hepatoma cells was purified approximately 13,000-fold with a reasonably high yield (34%) by extraction with sodium cholate, ammonium sulfate fractionation, solubilization with sodium dodecyl sulfate, column chromatographies on Sephadex G-150 in the presence of sodium dodecyl sulfate, and on DEAE-cellulose and CM-cellulose in the presence of Triton X-100.	DEAE-Cellulose	369-383	phospholipase A2 group IB	Rattus norvegicus	2-18
7450390-1	1980	Human pancreatic Deoxyribonuclease I (DNase I), inhibitor was partially purified from duodenal juice of healthy subjects collected in the Pancreozymin-Secretin test, by a procedure which included ammonium sulfate fractionation, DEAE cellulose fractionation, Sepharose 4B affinity chromatography, and gel filtration.	DEAE-Cellulose	228-242	deoxyribonuclease 1	Homo sapiens	38-45
6246130-5	1980	The biologically active material from the DEAE-cellulose column, when labeled with 125I, showed specific binding to EGF membrane receptors.	DEAE-Cellulose	42-56	epidermal growth factor	Mus musculus	116-119
6769429-1	1980	alpha-Lactalbumin was purified to apparent homogeneity from mouse milk by combined use of gel filtration, chromatography on DEAE-cellulose and hydroxyapatite, and concanavalin A-Sepharose affinity chromatography.	DEAE-Cellulose	124-138	lactalbumin, alpha	Mus musculus	0-17
7447641-1	1980	Proteinase inhibitors adsorbed from human serum on DEAE Sephadex A 25 0.25 or 0.3 mol/l NaCl were purified by affinity chromatography on a trypsin-Sepharose 4B column, by gel filtration, and by DEAE cellulose chromatography.	DEAE-Cellulose	194-208	endogenous retrovirus group K member 25	Homo sapiens	0-10
508812-4	1979	Extracted protein kinase resolved into three peaks on DEAE-cellulose chromatography.	DEAE-Cellulose	54-68	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	10-24
7430650-1	1980	alpha-Lactalbumin has been purified from mouse milk by the use of ammonium sulfate precipitation, Bio-Gel P-100 chromatography and DEAE-cellulose chromatography.	DEAE-Cellulose	131-145	lactalbumin, alpha	Mus musculus	0-17
6258031-5	1980	The activity was localized in the outer membrane of phase I bacteria, as was the in vitro PIF activity, and the two activities gave the same behavior in DEAE-cellulose chromatography.	DEAE-Cellulose	153-167	Pif	Mus musculus	90-93
42911-1	1979	Uroporphyrinogen I synthase [porphobilinogen ammonia-lyase (polymerizing), EC 4.3.1.8] from human erythrocytes was separated into two active protein peaks (A and B on DEAE-cellulose, by ammonium sulfate fractionation, on Sephadex G-100, and on DEAE-Sephadex A-50 with a NaCl gradient.	DEAE-Cellulose	167-181	hydroxymethylbilane synthase	Homo sapiens	0-27
231033-1	1979	A "double-alpha" c-type cytochrome, cytochrome c-555, 549, was isolated from the membrane fraction of an extreme thermophile, Thermus thermophilus HB8, and highly purified by chromatographies on DEAE-cellulose and Sephadex G-75 and by isoelectric focusing.	DEAE-Cellulose	195-209	sulfur oxidation c-type cytochrome SoxA	Thermus thermophilus HB8	36-48
500599-1	1979	Three charge forms of rat alpha-lactalbumin were separated by ion exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	93-107	lactalbumin, alpha	Rattus norvegicus	26-43
115864-2	1979	An enzyme which catalyzes the deamidation of thyroliberin (TRF; less than Glu-His-Pro-NH2) has been purified 110-fold from extracts of bovine anterior pituitary by ammonium sulfate fractionation, ion exchange chromatography on DEAE-cellulose, and gel filtration.	DEAE-Cellulose	227-241	interleukin 5	Bos taurus	59-62
41579-4	1979	The ribonuclease was extracted in the presence of EDTA from ribosomes and purified 118-rold by protamine sulphate precipitation, (NH4)2SO4 fractionation and chromatography on DEAE-cellulose.	DEAE-Cellulose	175-189	ribonuclease	Saccharomyces cerevisiae S288C	4-16
90677-1	1979	A new form of cytoplasmic glucose-6-phosphate dehydrogenase (E.C.1.1.1.49) was purified from rat liver by protamine sulfate precipitation, ammonium sulfate fractionation, ion exchange chromatography with diethylaminoethyl cellulose, and affinity chromatography with Cibacron blue agarose and NADP agarose.	DEAE-Cellulose	204-231	glucose-6-phosphate dehydrogenase	Rattus norvegicus	26-59
454845-4	1979	Under these conditions, thrombopoiesis-stimulating activity (thrombopoietin) was retained by DEAE cellulose (0/03 M citrate-phosphate buffer) and carboxymethyl cellulose (0/003 M citrate-phosphate buffer), and eluted with 0.4 M NaCl.	DEAE-Cellulose	93-107	thrombopoietin	Oryctolagus cuniculus	61-75
41651-1	1979	The major forms of human serum hexosaminidases A and B (Hex A and Hex B) were isolated from normal subjects and cancer patients using DEAE-cellulose.	DEAE-Cellulose	134-148	hexosaminidase subunit alpha	Homo sapiens	56-71
473685-1	1979	Isolation and partial purification of renin from human kidney was carried out as follows: defatting of the homogenized kidney; extraction with methyl cellosolve; chromatography on DEAE cellulose; affinity chromatography using immobilized pepstain.	DEAE-Cellulose	180-194	renin	Homo sapiens	38-43
226067-12	1979	DEAE-cellulose ion-exchange chromatography resolved four peaks of protein kinase activity.	DEAE-Cellulose	0-14	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	66-80
385058-1	1979	Porcine beta-casein was isolated by chromatography on DEAE-cellulose.	DEAE-Cellulose	54-68	casein beta	Bos taurus	8-19
445857-2	1979	Two, HEX A and HEX B, migrate in both DEAE cellulose and isoelectric focussing systems like their tissue counterparts.	DEAE-Cellulose	38-52	hexosaminidase subunit alpha	Homo sapiens	5-10
445857-2	1979	Two, HEX A and HEX B, migrate in both DEAE cellulose and isoelectric focussing systems like their tissue counterparts.	DEAE-Cellulose	38-52	hematopoietically expressed homeobox	Homo sapiens	5-8
445857-5	1979	Using DEAE-cellulose chromatography, HEX A, I, and B, can be clearly separated.	DEAE-Cellulose	6-20	hexosaminidase subunit alpha	Homo sapiens	37-52
43056-2	1979	The haptoglobin is adsorbed to DEAE-cellulose at pH 5.1 by batching.	DEAE-Cellulose	31-45	haptoglobin	Homo sapiens	4-15
107159-3	1979	Fractionation of the brain extract by DEAE-cellulose chromatography produces three protein fractions which metabolize TRH.	DEAE-Cellulose	38-52	thyrotropin releasing hormone	Homo sapiens	118-121
217872-2	1979	The enzyme succinic semialdehyde dehydrogenase from pig brain has been 2000-fold purified by a combination of DEAE-cellulose, hydroxyapatite, and AMP-Sepharose chromatography.	DEAE-Cellulose	110-124	aldehyde dehydrogenase 5 family member A1	Sus scrofa	11-46
464396-1	1979	Trehalase activities from mouse serum and kidney have been compared on ion exchange chromatography (DEAE-cellulose and SP-Sephadex).	DEAE-Cellulose	100-114	trehalase (brush-border membrane glycoprotein)	Mus musculus	0-9
162260-3	1979	ATPase A and ATPase B appear to be distinct enzymes as judged from their elution profiles obtained after DEAE-cellulose and ATP-Sepharose column chromatography, from their behavior towards actinomycin D, a DNA intercalating agent, and from their sensitivity to monovalent salt concentration.	DEAE-Cellulose	105-119	ATPase phospholipid transporting 8A2	Homo sapiens	13-21
162260-3	1979	ATPase A and ATPase B appear to be distinct enzymes as judged from their elution profiles obtained after DEAE-cellulose and ATP-Sepharose column chromatography, from their behavior towards actinomycin D, a DNA intercalating agent, and from their sensitivity to monovalent salt concentration.	DEAE-Cellulose	105-119	ATPase phospholipid transporting 8A2	Homo sapiens	0-3
41031-3	1979	Transketolase, sedoheptulose-7-phosphate: D-glyceraldehyde-3-phosphate glycolaldehyde-transferase [EC 2.2.1.1], was extracted from pig liver and purified 96-fold by ammonium sulfate fractionation, followed by column chromatography using DEAE-cellulose and a Sephadex G-200.	DEAE-Cellulose	237-251	transketolase	Sus scrofa	0-13
446070-8	1979	The diagnostic potential of the estimation of urinary NAG activity is enhanced by the separation of its isoenzymic forms by ion-exchange chromatography on DEAE-cellulose.	DEAE-Cellulose	155-169	O-GlcNAcase	Homo sapiens	54-57
743204-2	1978	Phosphoenolpyruvate carboxylase from the Crassulacean plant Bryophyllum fedtschenkoi has been purified to homogenetity by DEAE-cellulose treatment, (NH4)2SO4 fractionation,, and chromatography on DEAE-cellulose and hydroxyapatite.	DEAE-Cellulose	122-136	phosphoenolpyruvate carboxykinase 1	Homo sapiens	0-31
728471-7	1978	In the present study, a uteroglobin-like protein was purified to an apparent homogeneity from an extra-uterine tissue, rabbit lung, by successive chromatographies on hydroxyapatite, Sephadex G-75, SP-Sephadex, DEAE-cellulose and CM-cellulose.	DEAE-Cellulose	210-224	uteroglobin	Oryctolagus cuniculus	24-35
9762089-4	1978	A two-step separation and purification of elastin from the collagen-free extract is based on absorption of the acidic proteins on DEAE-cellulose and gel filtration through agarose.	DEAE-Cellulose	130-144	LOC100620140	Sus scrofa	42-49
547226-1	1979	Arginyl-tRNA synthetase has been purified approximately 550 fold from crude extract of human placenta by the following purification steps: Ammonium sulfate fractionation, chromatographies of DEAE-cellulose and CM-Sephadex and Sephadex G-100 gel filtration.	DEAE-Cellulose	191-205	arginyl-tRNA synthetase 1	Homo sapiens	0-23
214121-2	1978	Protein kinase activity in these proteins was fractionated by either phosphocellulose or DEAE-cellulose chromatography.	DEAE-Cellulose	89-103	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	0-14
308823-4	1978	A urinary colony-inhibiting factor was separated from the CSF on the first DEAE-cellulose column.	DEAE-Cellulose	75-89	colony stimulating factor 2	Homo sapiens	58-61
743204-2	1978	Phosphoenolpyruvate carboxylase from the Crassulacean plant Bryophyllum fedtschenkoi has been purified to homogenetity by DEAE-cellulose treatment, (NH4)2SO4 fractionation,, and chromatography on DEAE-cellulose and hydroxyapatite.	DEAE-Cellulose	196-210	phosphoenolpyruvate carboxykinase 1	Homo sapiens	0-31
31328-1	1978	Rat liver tyrosine aminotransferase was purified by chromatography on CM-Sephadex C-50 and DEAE-cellulose, (NH4)2SO4 fractionation and gel filtration on Sephadex G-200.	DEAE-Cellulose	91-105	tyrosine aminotransferase	Rattus norvegicus	10-35
364424-1	1978	T7 gene 6 exonuclease has been shown to have an RNase H activity as well as a double-strand specific DNase activity by the following experiments: The RNase H activity coelutes with the DNase activity from DEAE-cellulose, phosphocellulose, hydroxyapatite, and Sephadex G-200 columns.	DEAE-Cellulose	205-219	colicin E8	Escherichia coli	101-106
364424-1	1978	T7 gene 6 exonuclease has been shown to have an RNase H activity as well as a double-strand specific DNase activity by the following experiments: The RNase H activity coelutes with the DNase activity from DEAE-cellulose, phosphocellulose, hydroxyapatite, and Sephadex G-200 columns.	DEAE-Cellulose	205-219	colicin E8	Escherichia coli	185-190
361297-5	1978	Another small peak representing alpha-glucosidase was found in fresh extracts of cultured cells on DEAE-cellulose columns.	DEAE-Cellulose	99-113	sucrase-isomaltase	Homo sapiens	32-49
681363-2	1978	Cystathionine beta-synthase has been purified from human liver more than 3000-fold by a series of steps including high speed centrifugation, ammonium sulfate fractionation, chromatography on hydroxylapatite and DEAE-cellulose, gel filtration, preparative polyacrylamide gel electrophoresis, and glycerol density gradient centrifugation.	DEAE-Cellulose	211-225	cystathionine beta-synthase	Homo sapiens	0-27
708776-2	1978	Squid rhodopsin was extracted with solutions of fatty acid esters of sucrose (monolaurate and monostearate) and purified by DEAE-cellulose and concanavalin A-Sepharose affinity chromatography.	DEAE-Cellulose	124-138	rhodopsin	Homo sapiens	6-15
682973-1	1978	The isozymes of hexokinase in surgical specimens of human subcutaneous adipose tissue were separated by elution from DEAE-cellulose with linear KCl gradients at ph 7.4.	DEAE-Cellulose	117-131	hexokinase 1	Homo sapiens	16-26
659434-7	1978	2) Analyses of reaction products by sucrose gradient centrifugation and chromatography on Sephadex G-100 and DEAE-cellulose indicate that, PC I cleaves reoviral RNA endonucleolytically to a final mixture of mono- and oligonucleotides, whereas the only acid- or alcohol-soluble products of PC II are 5"-XMPs produced exonucleolytically.	DEAE-Cellulose	109-123	serpin family A member 5	Homo sapiens	139-143
744121-5	1978	When the dog kidney homogenate was fractionated on DEAE-cellulose, all of the erythropoietin activity was adsorbed to the exchanger in the presence of 0.01 M acetate buffer, pH 4.5, and was completely eluted by 0.1 M Na2HPO4-0.5 M NaCl, pH 8.	DEAE-Cellulose	51-65	erythropoietin	Canis lupus familiaris	78-92
715376-2	1978	The binding protein was identified as transcobalamin I (TCI) by DEAE cellulose ion-exchange chromatography, Sephadex G200 gel filtration and agar gel electrophoresis.	DEAE-Cellulose	64-78	transcobalamin 1	Homo sapiens	38-54
715376-2	1978	The binding protein was identified as transcobalamin I (TCI) by DEAE cellulose ion-exchange chromatography, Sephadex G200 gel filtration and agar gel electrophoresis.	DEAE-Cellulose	64-78	transcobalamin 1	Homo sapiens	56-59
81797-1	1978	alpha-1-Inhibitor3 (alpha-I3), a new enzyme-binding protein, was isolated from rat plasma by a combination of ammonium sulfate precipitation, ion exchange chromatography on DEAE cellulose and gel filtration on ultrogel AcA34.	DEAE-Cellulose	173-187	alpha-1-inhibitor III	Rattus norvegicus	0-18
81797-1	1978	alpha-1-Inhibitor3 (alpha-I3), a new enzyme-binding protein, was isolated from rat plasma by a combination of ammonium sulfate precipitation, ion exchange chromatography on DEAE cellulose and gel filtration on ultrogel AcA34.	DEAE-Cellulose	173-187	alpha-1-inhibitor III	Rattus norvegicus	20-28
28369-5	1978	C1q-p was found to partition with IgG during precipitation by ammonium sulfate and low ionic strength buffer as well as during column chromatography on DEAE-cellulose and G-200 Sephadex.	DEAE-Cellulose	152-166	complement C1q A chain	Homo sapiens	0-3
277914-1	1978	Homogeneous preparations of two forms of soluble cytochrome b5 have been obtained from bovine erythrocytes by successive chromatography on DEAE-cellulose, Bio-Gel P-60, and DEAE-Sephadex.	DEAE-Cellulose	139-153	cytochrome b5 type A	Bos taurus	49-62
670480-2	1978	Chromatography of whole kappa-casein on DEAE-cellulose separated 5 fractions.	DEAE-Cellulose	40-54	kappa-casein	Capra hircus	24-36
306347-2	1978	The colony stimulating factor (GM-CSF) from YSCM was able to be concentrated by absorption to DEAE-cellulose and subsequent elution.	DEAE-Cellulose	94-108	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	4-29
26676-1	1978	Lysophospholipase [EC 3.1.1.5] was solubilized from the cells of Vibrio parahaemolyticus with Triton X-100 and purified by the following procedure; precipitation with ammonium sulfate, acid treatment and ion exchange column chromatography using DEAE-cellulose, DEAE-Sephadex A-50, and CM-cellulose, successively.	DEAE-Cellulose	245-259	phospholipase B1	Homo sapiens	0-17
306347-2	1978	The colony stimulating factor (GM-CSF) from YSCM was able to be concentrated by absorption to DEAE-cellulose and subsequent elution.	DEAE-Cellulose	94-108	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	31-37
564141-5	1978	In the second procedure DEAE-cellulose filtration was used to isolate the TeBG-steroid complex for quantitation.	DEAE-Cellulose	24-38	sex hormone binding globulin	Homo sapiens	74-78
623774-3	1978	Renin was purified 30 000-fold from rat kidneys by chromatography on DEAE-cellulose and SP-Sephadex, and by affinity chromatography on pepstatinyl-Sepharose.	DEAE-Cellulose	69-83	renin	Rattus norvegicus	0-5
24408196-4	1978	The purification of L-2 includes ammonium sulfate fractionation, gelfiltration on Sephadex G-150 and gradient elution from a DEAE-cellulose column.	DEAE-Cellulose	125-139	seed linoleate 9S-lipoxygenase-2	Glycine max	20-23
203328-3	1978	Two classes of cyclic GMP binding site were demonstrated by kinetic analysis of cyclic [3H]GMP binding in the enzyme preparations eluted by 0.1 M potassium phosphate (pH 7.0) from DEAE cellulose.	DEAE-Cellulose	180-194	5'-nucleotidase, cytosolic II	Homo sapiens	22-25
203328-3	1978	Two classes of cyclic GMP binding site were demonstrated by kinetic analysis of cyclic [3H]GMP binding in the enzyme preparations eluted by 0.1 M potassium phosphate (pH 7.0) from DEAE cellulose.	DEAE-Cellulose	180-194	5'-nucleotidase, cytosolic II	Homo sapiens	91-94
318356-0	1978	Separation of beta-N-acetylglucosaminidase isoenzymes from liver and plasma of six mammalian species by DEAE-cellulose chromatography.	DEAE-Cellulose	104-118	O-GlcNAcase	Homo sapiens	14-42
652382-2	1978	This study undertook extraction and identification of ricin, a toxalbumine, from Iranian Ricinus communis L. Ricin, was extracted from the seeds using dilute acid solution, salted out with ammonium sulfate, and purified by Sephadex G - 75 and DEAE - cellulose column chromatography.	DEAE-Cellulose	243-259	ricin	Ricinus communis	54-59
624180-1	1978	Renin substrate (angiotensinogen) in unfractionated human plasma has been shown to exist in multiple forms by DEAE-cellulose chromatography and isoelectric focusing.	DEAE-Cellulose	110-124	renin	Homo sapiens	0-5
588590-0	1977	Purification of C-reactive protein on DEAE-cellulose by a simple two-step procedure utilizing the calcium-dependency of the protein.	DEAE-Cellulose	38-52	C-reactive protein	Homo sapiens	16-34
144600-2	1977	Phosphofructokinase to prepared is partially phosphorylated and may be fractioned into three distinct species with sedimentation coefficients of 30 S, 18 S and 13 S by chromatography of agarose gels, hydroxyapatite or DEAE-cellulose.	DEAE-Cellulose	218-232	ATP-dependent 6-phosphofructokinase, muscle type	Oryctolagus cuniculus	0-19
19463-2	1977	Human kidney gamma-glutamyl transpeptidase has been purified by a procedure involving Lubrol extraction, acetone precipitation, treatment with bromelain, and column chromatography on DEAE-cellulose and Sephadex G-150.	DEAE-Cellulose	183-197	inactive glutathione hydrolase 2	Homo sapiens	13-42
588268-1	1977	Argininosuccinate lyase (EC 4.3.2.1) was purified by (NH4)2SO4 fractionation, chromatography on DEAE-cellulose and gel filtration on Sephadex G-200.	DEAE-Cellulose	96-110	argininosuccinate lyase	Homo sapiens	0-23
21888-1	1977	DEAE cellulose "mini" columns at pH 7.4 retain testosterone (T) bound to testosterone binding globulin (TeBG), which can be eluted at pH 2.	DEAE-Cellulose	0-14	sex hormone binding globulin	Homo sapiens	73-102
21888-1	1977	DEAE cellulose "mini" columns at pH 7.4 retain testosterone (T) bound to testosterone binding globulin (TeBG), which can be eluted at pH 2.	DEAE-Cellulose	0-14	sex hormone binding globulin	Homo sapiens	104-108
902370-6	1977	Three peaks of enzymatically active renin were obtained after the DEAE-cellulose chromatography, with specific activities ranging from 206 to 166 and 85 Goldblatt units/mg protein, respectively.	DEAE-Cellulose	66-80	renin	Homo sapiens	36-41
891468-2	1977	The antiserum gave precipitin lines of complete identity to phosvitin and to vitellogenin which was isolated from hen plasma by DEAE-cellulose chromatography and by affinity chromatography using anti-phosvitin coupled to Sepharose 4B.	DEAE-Cellulose	128-142	putative uncharacterized protein LOC400499	Homo sapiens	77-89
18462-2	1977	CDP-diglyceride:inositol transferase, which catalyzes the final step of the de novo synthesis of phosphatidylinositol, was solubilized by sodium cholate from microsomes prepared from rat liver and purified by ammonium sulfate fractionation, sucrose density gradient centrifugation, and DEAE-cellulose column chromatography.	DEAE-Cellulose	286-300	cut-like homeobox 1	Rattus norvegicus	0-3
877516-0	1977	Comparison of biochemical properties of human serum B12 binders derived from sephadex and DEAE-cellulose chromatography.	DEAE-Cellulose	90-104	NADH:ubiquinone oxidoreductase subunit B3	Homo sapiens	52-55
921736-3	1977	Chromatography of transferrin AA on DEAE-cellulose separated four subfractions, each of which corresponded well with one band obtained by polyacrylamide gel electrophoresis.	DEAE-Cellulose	36-50	serotransferrin	Bos taurus	18-29
561063-1	1977	Myosin light chain kinase from frozen rabbit skeletal muscle was separated into two protein components by DEAE-cellulose column chromatography.	DEAE-Cellulose	106-120	myosin light chain kinase, smooth muscle	Oryctolagus cuniculus	0-25
889853-2	1977	Monoacylglycerol lipase was purified about 1200-fold by DEAE-cellulose, hydroxylapatite, SP-Sephadex and Sephadex G-100 column chromatography from rat liver whole homogenate.	DEAE-Cellulose	56-70	monoglyceride lipase	Rattus norvegicus	0-23
17398-1	1977	Carboxypeptidase B of the human pancreas was purified by chromatography on DEAE-cellulose and CM-cellulose columns.	DEAE-Cellulose	75-89	carboxypeptidase B1	Homo sapiens	0-18
196375-1	1977	Protein kinase from the bull myocardium tissue was separated by means of the stepped gradient of buffer concentrations on DEAE-cellulose.	DEAE-Cellulose	122-136	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	0-14
877516-9	1977	Of the 6 binders from DEAE-cellulose, only peaks eluted with 0.06 M and 0.1 M buffers from TCS delivered labelled B12 to these cells.	DEAE-Cellulose	22-36	NADH:ubiquinone oxidoreductase subunit B3	Homo sapiens	114-117
196375-3	1977	Protein kinase isolated at elution by 0.3 M potassium-phosphate buffer from DEAE-cellulose is less sensitive to cAMP than protein kinase isolated according to Kuo.	DEAE-Cellulose	76-90	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	0-14
196375-3	1977	Protein kinase isolated at elution by 0.3 M potassium-phosphate buffer from DEAE-cellulose is less sensitive to cAMP than protein kinase isolated according to Kuo.	DEAE-Cellulose	76-90	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	122-136
849464-3	1977	Removal of all 43 000-dalton material by hydroxyapatite chromatography is accompanied by disappearance of a very small 9 to 10 S boundary in analytical ultracentrifuge diagrams of DEAE-cellulose-purified 6.2S alpha-actinin.	DEAE-Cellulose	180-194	actinin, alpha 4	Gallus gallus	209-222
849464-4	1977	Approximately 95% of the protein in DEAE-cellulose and hydroxyapatite-purified alpha-actinin is the 100 000-dalton alpha-actinin polypeptide as estimated by SDS-polyacrylamide gel electrophoresis.	DEAE-Cellulose	36-50	actinin, alpha 4	Gallus gallus	115-128
849464-1	1977	Highly purified bovine cardiac alpha-actinin is obtained by successive chromatography on DEAE-cellulose and hydroxyapatite of a crude fraction obtained by salting out low ionic strength extracts of bovine cardiac muscle between 0 and 30% ammonium sulfate saturation.	DEAE-Cellulose	89-103	actinin, alpha 4	Gallus gallus	31-44
849471-2	1977	A description is given of the fractionation of kappa-casein on DEAE-cellulose using a pH gradient.	DEAE-Cellulose	63-77	casein kappa	Bos taurus	47-59
13840-2	1977	Glucokinase (ATP : D-glucose 6-phosphotransferase, EC 2.7.1.2) was extracted from pea seeds and purified by fractionation with (NH4)2SO4 and chromatography on DEAE-cellulose and Sephadex.	DEAE-Cellulose	159-173	glucokinase	Homo sapiens	0-11
12888-0	1977	A simple assay for galactokinase using DEAE-cellulose column chromatography.	DEAE-Cellulose	39-53	galactokinase 1	Homo sapiens	19-32
617778-2	1977	Purified prothrombin was applied to DEAE-cellulose chromatography after incubation with thrombin.	DEAE-Cellulose	36-50	prothrombin	Oryctolagus cuniculus	9-20
848749-0	1977	Use of borate buffers for purification of placental beta-glucuronidase on DEAE-cellulose.	DEAE-Cellulose	74-88	glucuronidase beta	Homo sapiens	52-70
617778-2	1977	Purified prothrombin was applied to DEAE-cellulose chromatography after incubation with thrombin.	DEAE-Cellulose	36-50	prothrombin	Oryctolagus cuniculus	12-20
1009123-6	1976	In addition, the three forms of human carboxypeptidase B differ in electrophoretic mobility in polyacrylamide gel electrophoresis and in chromatographic behavior on DEAE-cellulose.	DEAE-Cellulose	165-179	carboxypeptidase B1	Homo sapiens	38-56
11093-1	1976	Uteroglobin was obtained from 5 day pregnant rabbits and purified to homogeneity by Sephadex G 75 and DEAE-cellulose chromatographies.	DEAE-Cellulose	102-116	uteroglobin	Oryctolagus cuniculus	0-11
400950-4	1977	The main inhibitor, accounting for 90% of the total activity of serum, appears to be alpha 1-antitrypsin (alpha 1-AT) as identified by separation on DEAE-cellulose and Sephadex, by immunoelectrophoresis and by anticercarial protease activity of purified alpha 1-AT preparations.	DEAE-Cellulose	149-163	serpin family A member 1	Homo sapiens	85-104
400950-4	1977	The main inhibitor, accounting for 90% of the total activity of serum, appears to be alpha 1-antitrypsin (alpha 1-AT) as identified by separation on DEAE-cellulose and Sephadex, by immunoelectrophoresis and by anticercarial protease activity of purified alpha 1-AT preparations.	DEAE-Cellulose	149-163	serpin family A member 1	Homo sapiens	106-116
9189-1	1976	Tonin was purified from rat submaxillary glands by differential centrifugation, ammonium sulphate precipitation, gel filtration on Sephadex G150, and by ion-exchange chromatography on DEAE-cellulose, phospho-cellulose, SP-Sephadex C25, and SP-Sephadex C50.	DEAE-Cellulose	184-198	kallikrein 1-related peptidase C2	Rattus norvegicus	0-5
1009925-1	1976	The major C4 component of human serum cholinesterase was highly purified by a two-step procedure involving chromatography on DEAE-cellulose and preparative disc electrophoresis.	DEAE-Cellulose	125-139	butyrylcholinesterase	Homo sapiens	38-52
1010840-4	1976	After carboxymethylation of the fibroin, it was fractionated by ammonium sulfate precipitation, Sephadex G-200 gel filtration and DEAE-cellulose column chromatography.	DEAE-Cellulose	130-144	fibroin light chain	Bombyx mori	32-39
1087637-2	1976	Human urinary kallikrein [EC 3.4.21.8] (HUK) was purified about 200-fold with an overall yield of 40 percent from crude powder by DEAE-cellulose chromatography, acetone fractionation, Sephadex G-100 gel filtration and DEAE-Sephadex A-50 chromatography.	DEAE-Cellulose	130-144	kallikrein related peptidase 4	Homo sapiens	14-24
10611-1	1976	Aminopeptidase activity of three fractions of human erythrocytes (membranes free of hemoglobin; hemolysate free of membranes; enzyme protein fraction made free of hemoglobin by DEAE-cellulose) was measured by a NADH dependent optical test using asparaginyl1-angiotension II-amide as substrate.	DEAE-Cellulose	177-191	carboxypeptidase Q	Homo sapiens	0-14
12146-1	1976	Oxytocinase (cystyl-aminopeptidase) [EC 3.4.11.3] was isolated from monkey placenta in a purified form by a six-step prodedure comprising extraction from monkey placenta homogenate, ammonium sulfate fractionation, repeated chromatography on hydroxylapatite, chromatography on a column of DEAE-cellulose and gel filtration on a column of Sephadex G-200.	DEAE-Cellulose	288-302	leucyl and cystinyl aminopeptidase	Homo sapiens	0-11
947629-0	1976	A method for galactose-1-phosphate uridyltransferase assay and the separation of its isozymes by DEAE-cellulose column chromatography.	DEAE-Cellulose	97-111	galactose-1-phosphate uridylyltransferase	Homo sapiens	13-52
947629-1	1976	A simplified radioactive assay for galactose-1-phosphate uridyltransferase (EC 2.7.7.12) using a small DEAE-cellulose column for the identification of the endproduct (uridine diphosphate galactose) is described.	DEAE-Cellulose	103-117	galactose-1-phosphate uridylyltransferase	Homo sapiens	35-74
947629-3	1976	Furthermore, different isozymes of red blood cell galactose-1-phosphate uridyltransferase were separated on DEAE-cellulose columns.	DEAE-Cellulose	108-122	galactose-1-phosphate uridylyltransferase	Homo sapiens	50-89
941901-2	1976	Identification and quantitation of hex A, amounting to 3.5%-6.9% of total beta hexosaminidase activity, has been obtained by cellulose acetate gel electrophoresis, DEAE-cellulose ion-exchange chromatography, radial immunodiffusion, and radioimmunoassay.	DEAE-Cellulose	164-178	hexosaminidase subunit alpha	Homo sapiens	35-40
1277502-0	1976	Separation of folate binding protein from human serum by DEAE-cellulose column chromatography.	DEAE-Cellulose	57-71	folate receptor alpha	Homo sapiens	14-36
962854-10	1976	The neutral beta-galactosidase activity can be resolved into two forms by DEAE-cellulose chromatography.	DEAE-Cellulose	74-88	galactosidase beta 1	Homo sapiens	12-30
5284-2	1976	They are identical with the previously purified molecular fomrs, GABAT I and GABAT II, separated by DEAE cellulose chromatography.	DEAE-Cellulose	100-114	4-aminobutyrate aminotransferase	Sus scrofa	65-70
931995-12	1976	25- and 26-Hydroxylase activities were separated partially by chromatography of subtilisintreated cytochrome P-450 fraction on DEAE-cellulose.	DEAE-Cellulose	127-141	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	98-114
5108-6	1976	A small amount of a side product was removed on DEAE-cellulose at pH 7.2 to give an overall recovery of insulin of 70-80%.	DEAE-Cellulose	48-62	insulin	Homo sapiens	104-111
1268202-1	1976	Subcellular fractionation of oviduct tissue from estrogen-treated chicks indicated that the bulk of the protein kinase activity of this tissue is located in the cytoplasmic and nuclear fractions, DEAE-cellulose chromatography of cytosol revealed a major peak of cAMP stimulatable activity eluting at 0.2 M KCl.	DEAE-Cellulose	196-210	tyrosine kinase 2	Gallus gallus	104-118
1278176-4	1976	Renin was extracted from 100 kg of hog kidneys and semi-purified by ammonium sulfate precipitations and chromatography on DEAE-cellulose.	DEAE-Cellulose	122-136	renin	Homo sapiens	0-5
5284-2	1976	They are identical with the previously purified molecular fomrs, GABAT I and GABAT II, separated by DEAE cellulose chromatography.	DEAE-Cellulose	100-114	4-aminobutyrate aminotransferase	Sus scrofa	77-82
57921-4	1976	A polypeptide, homologous to human J chain, was isolated by chromatography on DEAE-cellulose from the reduced and alkylated X. laevis hexameric macroglobulin.	DEAE-Cellulose	78-92	joining chain of multimeric IgA and IgM	Homo sapiens	35-42
816379-1	1976	Renin substrate was initially extracted from human plasma by (NH4)2SO4 followed by chromatography on Sephadex G-150, DEAE cellulose, calcium phosphate gel, isoelectric focusing and preparative polyacrylamide gel electrophoresis.	DEAE-Cellulose	117-131	renin	Homo sapiens	0-5
1228249-3	1975	N-IgG was purified from normal rabbit sera by DEAE-cellulose chromatography.	DEAE-Cellulose	46-60	immunoglobulin heavy chain (V7183 family)	Mus musculus	2-5
139173-1	1976	The specific elution of rabbit skeletal muscle phosphofructokinase (PFK) from DEAE-cellulose is studied in the linear gradient of different allosteric ligands.	DEAE-Cellulose	78-92	ATP-dependent 6-phosphofructokinase, muscle type	Oryctolagus cuniculus	68-71
178333-3	1976	Positive strains produce cholesterol esterase which was obtained from DEAE-cellulose column fractions of 18 h broth cultures.	DEAE-Cellulose	70-84	carboxyl ester lipase	Homo sapiens	25-45
1084-2	1975	This purified FABP represents two protein bands that bind PGA on polyacrylamide disc gel electrophoreis, elutes from DEAE-cellulose in 0.001 M phosphate buffer, stains positive with PAS, Elutes from concanavalin A Sepharose affinity columns with methyl alpha-mannoside, and shows three major peaks (pl =6.8, 7.5, 8.2) by isotric focusing.	DEAE-Cellulose	117-131	folate receptor alpha	Homo sapiens	14-18
182121-5	1976	Radioactivity eluted in the 0.02 and 0.06M-phosphate regions on DEAE-cellulose DE-52 appears to be due to [3H]aldosterone binding to glucocorticoid-specific "GR" receptors and to transcortin respectively, since labelling was greater with corticosterone even at 10 nM than with the mineralocorticoid at 100nM and since [14C]corticosterone bound to blood serum transcortin was always co-chromatographed in the 0.06M-phosphate region.	DEAE-Cellulose	64-78	serpin family A member 6	Rattus norvegicus	179-190
182121-5	1976	Radioactivity eluted in the 0.02 and 0.06M-phosphate regions on DEAE-cellulose DE-52 appears to be due to [3H]aldosterone binding to glucocorticoid-specific "GR" receptors and to transcortin respectively, since labelling was greater with corticosterone even at 10 nM than with the mineralocorticoid at 100nM and since [14C]corticosterone bound to blood serum transcortin was always co-chromatographed in the 0.06M-phosphate region.	DEAE-Cellulose	64-78	serpin family A member 6	Rattus norvegicus	359-370
814122-1	1976	A rapid method is described for the purification of galactose-1-phosphate uridylyltransferase (EC 2.7.7.12) from human red blood cells by the use of DEAE-cellulose and two steps of affinity chromatography on a "uridine-aminohexyl" agarose column.	DEAE-Cellulose	149-163	galactose-1-phosphate uridylyltransferase	Homo sapiens	52-93
1270407-3	1976	On thecolumn, the C1 esterase inhibitor activity was found to coincide with Clr but not C1s (another subcomponent of the first component)  C1r was isolated from the euglobulin fraction of human serum by DEAE-cellulose column chromatograph.	DEAE-Cellulose	203-217	serpin family G member 1	Homo sapiens	18-39
1052169-0	1976	Separation of human hemoglobins by DEAE-cellulose chromatography using glycine-KCN-NaC1 developers.	DEAE-Cellulose	35-49	nucleus accumbens associated 1	Homo sapiens	83-87
53072-5	1975	Anti-beta-glucuronidase inhibitor isolated from human serum, by fractionation with (NH4)2 SO4 followed by DEAE-cellulose, Sephadex G-200 and Sepharose 4B chromatography, was identified as alpha2-macroglobulin by using ultracentrifuge analysis and immunoelectrophoresis.	DEAE-Cellulose	106-120	LOW QUALITY PROTEIN: alpha-2-macroglobulin	Oryctolagus cuniculus	188-208
1204284-6	1975	N-Acetyl-beta-D-glucosaminidase was resolved into its component forms by chromatography on microcolumns of DEAE-cellulose coupled with continuous automated assay of activity in the column effluent.	DEAE-Cellulose	107-121	O-GlcNAcase	Homo sapiens	0-31
1183035-2	1975	The A, B, I1 and I2 forms of N-acetyl-beta-glucosaminidase present in urine, serum, kidney, liver and cerebral spinal fluid were separated on DEAE-cellulose and their presence confirmed by cellogel electrophoresis.	DEAE-Cellulose	142-156	protein phosphatase 1 regulatory inhibitor subunit 1A	Homo sapiens	10-58
169257-2	1975	Angiotensin-converting enzyme has been solubilized from a particulate fraction of rabbit lung and purified to apparent homogeneity in 11% yield by a procedure including fractionation with DEAE-cellulose and calcium phosphate gel, elution from Sephadex G-200, and lectin affinity chromatography.	DEAE-Cellulose	188-202	angiotensin-converting enzyme	Oryctolagus cuniculus	0-29
1176817-3	1975	A modification of the microchromatographic procedure for Hb-A2 which utilizes DEAE-cellulose (Reference 1) allows the quantitation of Hb-A2 without interference from any Hb-S in the sample.	DEAE-Cellulose	78-92	hemoglobin subunit alpha 2	Homo sapiens	57-62
1176817-3	1975	A modification of the microchromatographic procedure for Hb-A2 which utilizes DEAE-cellulose (Reference 1) allows the quantitation of Hb-A2 without interference from any Hb-S in the sample.	DEAE-Cellulose	78-92	hemoglobin subunit alpha 2	Homo sapiens	134-139
237905-1	1975	Gamma-Glutamyl transpeptidase was purified from rat kidney by a procedure involving Lubrol extraction, acetone precipitation, ammonium sulfate fractionation, treatment with bromelain, and column chromatography on DEAE-cellulose and Sephadex G-100.	DEAE-Cellulose	213-227	gamma-glutamyltransferase 1	Rattus norvegicus	0-29
813784-1	1975	Pyruvate kinase (PK-II) isoenzyme from rabbit adrenal cortex was isolated by chromatography on DEAE-cellulose during long-term incubation in the cold.	DEAE-Cellulose	95-109	pyruvate kinase PKLR	Oryctolagus cuniculus	0-15
808238-4	1975	The purification technique has the following characteristics: (1) in optimal experiments, 3000-fold purification of enzyme was obtained; (2) the yield of enzyme was as great as 25%; (3) the binding of histaminase to the amine groups of the cadaverine appears to represent a true "affinity" phenomenon since enzyme bound to DEAE-cellulose under neutral pH conditions was eluted at much lower concentrations of NaCl (less than 0.4 M).	DEAE-Cellulose	323-337	amine oxidase copper containing 1	Homo sapiens	201-212
1201740-2	1975	Human thyroglobulin was purified by combined DEAE-cellulose and affinity chromatography using Sepharose 4B-bound Concanavalin A.	DEAE-Cellulose	45-59	thyroglobulin	Homo sapiens	6-19
1113-1	1975	The modified procedure for rabbit skeletal muscle phosphofructokinase (PFK) purification is worked out utioizing the method of specific elution from DEAE-cellulose in 0.1 M tris-EDTA-phosphate pH 8.0 with 10 mM citrate.	DEAE-Cellulose	149-163	ATP-dependent 6-phosphofructokinase, muscle type	Oryctolagus cuniculus	71-74
234459-5	1975	The same detergent solubilizes the microsomal squalene epoxidase and the resulting supernatant can be separated into two components, A and B, by DEAE-cellulose chromatography.	DEAE-Cellulose	145-159	squalene epoxidase	Rattus norvegicus	46-64
1125255-2	1975	Lipoyl dehydrogenase (NADH: lipoamide oxidoreductase, ED 1.6.4.3) and two asparagusate dehydrogenases from asparagus mitochondria were purified by a series of steps, freezing and thawing, sodium dodecylsulfate extraction, and chromatography on Sephadex G-200 and DEAE-cellulose.	DEAE-Cellulose	263-277	dihydrolipoamide dehydrogenase	Homo sapiens	0-20
234808-2	1975	The inactive form becomes active after exposure to pH 2.5 at 4 degrees C. If extracts are chromatographed on DEAE cellulose, the inactive renin dissociates into active renin plus a renin inhibitor (molecular weight about 13,000).	DEAE-Cellulose	109-123	LOW QUALITY PROTEIN: renin	Oryctolagus cuniculus	138-143
234808-2	1975	The inactive form becomes active after exposure to pH 2.5 at 4 degrees C. If extracts are chromatographed on DEAE cellulose, the inactive renin dissociates into active renin plus a renin inhibitor (molecular weight about 13,000).	DEAE-Cellulose	109-123	LOW QUALITY PROTEIN: renin	Oryctolagus cuniculus	168-173
234808-2	1975	The inactive form becomes active after exposure to pH 2.5 at 4 degrees C. If extracts are chromatographed on DEAE cellulose, the inactive renin dissociates into active renin plus a renin inhibitor (molecular weight about 13,000).	DEAE-Cellulose	109-123	LOW QUALITY PROTEIN: renin	Oryctolagus cuniculus	168-173
1125183-1	1975	NADPH-adrenodoxin reductase from steer adrenal cortex mitochrondria has been purified to homogeneity (on sodium dodecyl sulfate polyacrylamide gel electrophoresis) by chromatography on DEAE-cellulose, Sephadex, and hydroxylapatite.	DEAE-Cellulose	185-199	ferredoxin reductase	Bos taurus	6-27
1191562-1	1975	Two molecular forms of Fe1-transferrin molecule can be demonstrated by anion-exchange chromatography on columns of DEAE-cellulose, pH 7.90.	DEAE-Cellulose	115-129	transferrin	Homo sapiens	27-38
1129247-1	1975	Two isoenzymes of pyruvate kinase--PK-1 and PK-2 were obtained from the cortical layer of rabbit kidney by the method of chromatography on DEAE-cellulose.	DEAE-Cellulose	139-153	pyruvate kinase PKLR	Oryctolagus cuniculus	18-33
235578-2	1975	Beta-Casein was separated from buffalo"s milk by the method of Warner (1944) and purified by DEAE-cellulose chromatography.	DEAE-Cellulose	93-107	casein beta	Bos taurus	0-11
236080-1	1975	Protein kinase activity of rat testis homogenate was separated into five fractions by means of pH 4.8 acidification and DEAE-cellulose chromatography.	DEAE-Cellulose	120-134	KIT proto-oncogene receptor tyrosine kinase	Rattus norvegicus	0-14
1242082-1	1975	Testicular androgen binding protein (ABP) was purified from the epididymis of 1500 adult rabbits by the sequential use of ammonium sulphate precipitation, ion exchange chromatography on DEAE cellulose, gel filtration on Sephadex G-200, hydroxyl-apatite chromatography and preparative polyacrylamide gel electrophoresis.	DEAE-Cellulose	186-200	sex hormone-binding globulin	Oryctolagus cuniculus	37-40
1126343-14	1975	Chromatographic fractionation of whole kappa-casein on DEAE-cellulose also led to the separation of several fractions, the main characteristics of which are presented.	DEAE-Cellulose	55-69	kappa-casein	Ovis aries	39-51
51701-3	1975	The second, detectable with anti-membrane antiserum after absorption with fibrinogen remained with the fibrinogen-like antigen during isoelectric precipitation at pH 4.7, electrophoresis at pH 8.6 and chromatography on DEAE cellulose.	DEAE-Cellulose	219-233	fibrinogen beta chain	Homo sapiens	74-84
51701-3	1975	The second, detectable with anti-membrane antiserum after absorption with fibrinogen remained with the fibrinogen-like antigen during isoelectric precipitation at pH 4.7, electrophoresis at pH 8.6 and chromatography on DEAE cellulose.	DEAE-Cellulose	219-233	fibrinogen beta chain	Homo sapiens	103-113
1182212-1	1975	Rat hemopexin was purified by a procedure involving three different steps : ammonium sulfate precipitation, rivanol precipitation and DEAE-cellulose chromatography with concave gradient of molarity.	DEAE-Cellulose	134-148	hemopexin	Rattus norvegicus	4-13
16658848-5	1974	While diethylaminoethyl cellulose chromatography of plant extracts separated nitrate reductase from the bulk (90%) of the phosphatase and caused a decrease in the NADPH activity, the residual level of phosphatase was sufficient to account for the apparent NADPH nitrate reductase activity.	DEAE-Cellulose	6-33	chalcone reductase CHR1	Glycine max	85-94
236177-2	1975	Two forms of guiena pig brain GABA-T were isolated by DEAE-cellulose chromatography and designated as GABA-T-I and II, corresponding to an anionic and a cationic form.	DEAE-Cellulose	54-68	4-aminobutyrate aminotransferase	Sus scrofa	30-36
1198655-0	1975	A DEAE cellulose column method using predosed 57Co cyanocobalamin and pooled serum for measuring vitamin B12 in serum.	DEAE-Cellulose	2-16	NADH:ubiquinone oxidoreductase subunit B3	Homo sapiens	105-108
4455221-1	1974	The isolation of a salt-soluble homogeneous elastin from the aortas of lathyritic chicks by chromatography on DEAE-cellulose and salt precipitation is described.	DEAE-Cellulose	110-124	elastin	Ovis aries	44-51
5073743-1	1972	Preparations of ox spleen cathepsin B1 have been found to give multiple peaks of activity upon chromatography on DEAE-cellulose in NaCl gradients or by equilibrium chromatography in 0.05m-NaCl.	DEAE-Cellulose	113-127	cathepsin B	Homo sapiens	26-38
4116220-0	1972	Purification of human serum hemopexin by chromatography on DEAE-cellulose.	DEAE-Cellulose	59-73	hemopexin	Homo sapiens	28-37
4463937-2	1974	Triose phosphate isomerase was prepared by chromatography on DEAE-cellulose of an (NH(4))(2)SO(4) fraction of an extract of homogenized chicken breast muscle.	DEAE-Cellulose	61-75	triosephosphate isomerase 1	Gallus gallus	0-26
4454851-2	1974	Highly purified C-reactive protein extracted by chromatography on DEAE-cellulose].	DEAE-Cellulose	66-80	C-reactive protein	Homo sapiens	16-34
4748828-4	1973	Xenopus laevis liver gamma-glutamylcysteine synthetase was purified 324-fold by saline-bicarbonate extraction, protamine sulphate precipitation, CM-cellulose and DEAE-cellulose column chromatography, and gel filtration.	DEAE-Cellulose	162-176	glutamate-cysteine ligase, catalytic subunit	Rattus norvegicus	21-54
5441375-1	1970	Cholinesterase was purified from human serum by a three-stage procedure involving chromatography on DEAE-cellulose at pH4.0, an electrofocusing technique and gel filtration on Sephadex G-200.	DEAE-Cellulose	100-114	butyrylcholinesterase	Homo sapiens	0-14
5445687-2	1970	The isolation of human plasma prekallikrein was achieved by fractionating human plasma on diethylaminoethyl cellulose (DEAE) in the presence of heparin.2.	DEAE-Cellulose	90-117	kallikrein B1	Homo sapiens	23-43
4251126-7	1971	Plasminogen and plasmin were found on a DEAE-cellulose chromatogram of serum overlapping peaks 2 and 3.	DEAE-Cellulose	40-54	plasminogen	Homo sapiens	16-23
5339544-1	1966	Pepsinogen C and pepsin C from the pig have been further purified by chromatography on DEAE-cellulose and by exclusion chromatography and the specific activities (with haemoglobin substrate) found are higher than those previously reported.	DEAE-Cellulose	87-101	progastricsin	Sus scrofa	0-12
5703738-0	1968	[Some properties of prothrombin after chromatography on DEAE-cellulose].	DEAE-Cellulose	56-70	coagulation factor II, thrombin	Homo sapiens	20-31
5966283-2	1966	Pyruvate kinase (ATP-pyruvate phosphotransferase, EC 2.7.1.40) from Ehrlich ascites-tumour cells was purified approximately fivefold by chromatography on DEAE-cellulose.	DEAE-Cellulose	154-168	pyruvate kinase PKLR	Oryctolagus cuniculus	0-15
5822576-1	1969	Chromatographic, ultracentrifugal, and related studies of the fibrinogen of a patient with a congenital disorder of fibrinogen (fibrinogen "Baltimore" have provided evidence of structural differences from normal.Diethylaminoethyl-cellulose (DEAE-cellulose) gradient elution chromatography demonstrated two major peaks in the elution pattern of fibrinogen Baltimore as was the case for normal fibrinogen.	DEAE-Cellulose	241-255	fibrinogen beta chain	Homo sapiens	116-126
5822576-1	1969	Chromatographic, ultracentrifugal, and related studies of the fibrinogen of a patient with a congenital disorder of fibrinogen (fibrinogen "Baltimore" have provided evidence of structural differences from normal.Diethylaminoethyl-cellulose (DEAE-cellulose) gradient elution chromatography demonstrated two major peaks in the elution pattern of fibrinogen Baltimore as was the case for normal fibrinogen.	DEAE-Cellulose	241-255	fibrinogen beta chain	Homo sapiens	116-126
5822576-1	1969	Chromatographic, ultracentrifugal, and related studies of the fibrinogen of a patient with a congenital disorder of fibrinogen (fibrinogen "Baltimore" have provided evidence of structural differences from normal.Diethylaminoethyl-cellulose (DEAE-cellulose) gradient elution chromatography demonstrated two major peaks in the elution pattern of fibrinogen Baltimore as was the case for normal fibrinogen.	DEAE-Cellulose	241-255	fibrinogen beta chain	Homo sapiens	116-126
5822576-1	1969	Chromatographic, ultracentrifugal, and related studies of the fibrinogen of a patient with a congenital disorder of fibrinogen (fibrinogen "Baltimore" have provided evidence of structural differences from normal.Diethylaminoethyl-cellulose (DEAE-cellulose) gradient elution chromatography demonstrated two major peaks in the elution pattern of fibrinogen Baltimore as was the case for normal fibrinogen.	DEAE-Cellulose	241-255	fibrinogen beta chain	Homo sapiens	116-126
4388685-7	1968	(4) Deproteinization of DEAE-cellulose supernatants results in a complete loss of G6PD-inactivating ability; moreover, kinetic experiments performed with the extracts lacking pyrophosphatase strongly support the view that the inactivating protein is an enzyme, although its mechanism is not clear.	DEAE-Cellulose	24-38	glucose-6-phosphate dehydrogenase	Rattus norvegicus	82-86
5941349-11	1966	A 400-500-fold purification of the ribonuclease inhibitor was achieved by ammonium sulphate fractionation, treatment with calcium phosphate gel and DEAE-cellulose chromatography.	DEAE-Cellulose	148-162	ribonuclease/angiogenin inhibitor	Rattus norvegicus	35-57
5944237-2	1966	An 870-fold purification of glucokinase from rat liver is described which involves ammonium sulphate fractionation and the use of DEAE-Sephadex, DEAE-cellulose and polyacrylamide columns.	DEAE-Cellulose	145-159	glucokinase	Rattus norvegicus	28-39
14102873-6	1964	A 120-fold purification of the proteinase was obtained from the cell-free culture medium by ammonium sulfate fractionation, calcium phosphate gel treatment, and chromatography on diethylaminoethyl cellulose.	DEAE-Cellulose	179-206	prtP	Lactococcus lactis	31-41
5938660-2	1966	Galactokinase has been purified from the liver of young pigs by high-speed centrifugation, chromatography on Sephadex G-100 and DEAE-cellulose, and ammonium sulphate fractionation.	DEAE-Cellulose	128-142	galactokinase	Saccharomyces cerevisiae S288C	0-13
16749124-12	1965	Liver lysosomal beta-galactosidase exists in multiple forms that can be separated on DEAE-cellulose, and the enzyme components that are bound to the membrane appear to be similar to those of the lysosome sap.	DEAE-Cellulose	85-99	galactosidase, beta 1	Rattus norvegicus	16-34
4285846-0	1966	Investigation of myosin heterogeneity observed during chromatography on diethylaminoethyl cellulose.	DEAE-Cellulose	72-99	myosin heavy chain 14	Homo sapiens	17-23
14110749-1	1963	gamma-Globulin fractions isolated from guinea-pig serum by chromatography on diethylaminoethyl cellulose exhibited all the properties of kallikrein.	DEAE-Cellulose	77-104	kallikrein related peptidase 4	Homo sapiens	137-147
14035995-5	1962	Chromatography on DEAE-cellulose separated thrombin from thrombokinase.	DEAE-Cellulose	18-32	coagulation factor II, thrombin	Bos taurus	43-51
33443641-2	2021	RESULTS: The phospholipase A2 (PLA2) has been apparently purified from the venom of Egyptian honey bee (Apis mellifera lamarckii) 8.9-fold to a very high specific activity of 6033 U/mg protein using DEAE-cellulose and Sephacryl S-300 columns.	DEAE-Cellulose	199-213	phospholipase A2	Apis mellifera	13-29
14455076-0	1962	Renin purification by DEAE cellulose chromatography.	DEAE-Cellulose	22-36	renin	Homo sapiens	0-5
13866571-0	1962	Separation of leucylaminopeptidase components in normal human sera by DEAE cellulose column chromatography.	DEAE-Cellulose	70-84	leucine aminopeptidase 3	Homo sapiens	14-34
13916294-0	1961	The use of DEAE cellulose in the preparation of a factor VIII (AHG)-free bovine fibrinogen reagent.	DEAE-Cellulose	11-25	coagulation factor VIII	Bos taurus	50-61
13716724-0	1961	Qunatitative determination of the minor hemoglobin component Hb-A2 by DEAE-cellulose chromatography.	DEAE-Cellulose	70-84	hemoglobin subunit alpha 2	Homo sapiens	61-66
33443641-2	2021	RESULTS: The phospholipase A2 (PLA2) has been apparently purified from the venom of Egyptian honey bee (Apis mellifera lamarckii) 8.9-fold to a very high specific activity of 6033 U/mg protein using DEAE-cellulose and Sephacryl S-300 columns.	DEAE-Cellulose	199-213	phospholipase A2	Apis mellifera	31-35
25907067-4	2015	The catalytic activities (kcat) of the free, PANI, PAMP, and magnetic DEAE-cellulose were determined to be 4.0, 2.05, 0.59, and 0.042 mM/min mg protein, respectively.	DEAE-Cellulose	70-84	adrenomedullin	Homo sapiens	51-55
33141041-7	2021	Thermostable alpha-amylase was purified by 70% ammonium sulfate precipitation, DEAE-cellulose ion-exchange chromatography, and dialysis, with a 51-purification fold and 30% yield recovery.	DEAE-Cellulose	79-93	probable alpha-amylase 2	Malus domestica	13-26
32553949-3	2020	In this study, an acidic polysaccharide (PRP-2) was obtained from PR by ultrasonic assisted extraction and secondary column chromatography purification (Diethylaminoethyl cellulose-52 (DEAE-52) and Sephadex G-100).	DEAE-Cellulose	153-180	transmembrane protein 171	Homo sapiens	41-46
30832884-1	2019	Two polysaccharide fractions (TSP-1 and TSP-2) with molecular weights of 833.6 kDa and 81.6 kDa were isolated from Toona sinensis leaves (Meliaceae) by hot water extraction, DEAE Cellulose-52 chromatography and Sephacryl S-400 gel permeation chromatography.	DEAE-Cellulose	174-188	tumor suppressor region 1	Mus musculus	30-35
30832884-1	2019	Two polysaccharide fractions (TSP-1 and TSP-2) with molecular weights of 833.6 kDa and 81.6 kDa were isolated from Toona sinensis leaves (Meliaceae) by hot water extraction, DEAE Cellulose-52 chromatography and Sephacryl S-400 gel permeation chromatography.	DEAE-Cellulose	174-188	tumor suppressor region 2	Mus musculus	40-45
26869383-2	2016	MATERIALS AND METHODS: Hsp90 was extracted using glass beads and ultracentrifugation from yeast cells and purified by ion exchange chromatography (DEAE-cellulose) and followed by affinity chromatography (hydroxyapatite).	DEAE-Cellulose	147-161	Hsp90 family chaperone HSP82	Saccharomyces cerevisiae S288C	23-28
26478094-3	2016	The polysaccharide, AMPS-a, was obtained from the ethanol-extracted debris of Flos A. manihot by successive purification through DEAE-cellulose-52 and Sephadex G-100 column.	DEAE-Cellulose	129-143	adenylosuccinate lyase	Homo sapiens	20-24
32744543-1	2020	A water-soluble neutral homopolysaccharide (PLP-1) was obtained from the roots of Pueraria lobata by DEAE cellulose and Sephadex G-200 gel chromatography purification.	DEAE-Cellulose	101-115	proteolipid protein 1	Homo sapiens	44-49
29155159-2	2018	PRG1-1 has a molecular weight of 630kDa and was extracted and purified using DEAE-cellulose and gel filtration chromatography from crude polysaccharide extract of R. griseocarnosa sporocarp.	DEAE-Cellulose	77-91	PRG1	Homo sapiens	0-4
26130925-4	2015	METHODS: The Pax6 transcription factor was purified by heparin agarose affinity chromatography and DEAE cellulose chromatography techniques from the developing zebrafish embryos.	DEAE-Cellulose	99-113	paired box 6a	Danio rerio	13-17
25536026-1	2015	A new acidic polysaccharide (PLP) was isolated and characterized from Plantago asiatic L. seeds by hot alkali extraction and chromatographic purification using DEAE cellulose and Sephacryl S-400 columns.	DEAE-Cellulose	160-174	proteolipid protein 1	Homo sapiens	29-32
30364910-12	2015	CONCLUSIONS: Separation of proteins and particularly of BuChE on a chromatographic DEAE Cellulose column can be considered as a method for separation and purification of BuChE from human plasma.	DEAE-Cellulose	83-97	butyrylcholinesterase	Homo sapiens	56-61
30364910-12	2015	CONCLUSIONS: Separation of proteins and particularly of BuChE on a chromatographic DEAE Cellulose column can be considered as a method for separation and purification of BuChE from human plasma.	DEAE-Cellulose	83-97	butyrylcholinesterase	Homo sapiens	170-175
25339497-2	2015	In the present study, human S100A4 protein was expressed in Escherichia coli (E. coli) BL21 (DE3), successfully purified by diethylaminoethyl cellulose anion-exchange chromatography and identified by western blot analysis.	DEAE-Cellulose	124-151	S100 calcium binding protein A4	Homo sapiens	28-34
25374234-3	2014	HSP70 was purified from renal cell carcinoma specimens by serial column chromatography on Con A-sepharose, PD-10, ADP-agarose and DEAE-cellulose, and finally subjected to fast protein liquid chromatography (FPLC).	DEAE-Cellulose	130-144	heat shock protein family A (Hsp70) member 4	Homo sapiens	0-5
23987429-1	2013	The extracellular polysaccharide (LEP) produced by Lachnum YM281 was obtained from the fermentation broth, and LEP-1b with molecular weight of 4.02x10(4) Da was separated and sequentially purified through DEAE-cellulose 52 column chromatography and Sepharose CL-6B column chromatography.	DEAE-Cellulose	205-219	leptin	Mus musculus	34-37
24654772-2	2014	The purified polysaccharide AP1-1 was obtained from PE by macroporous adsorption resin chromatography, DEAE cellulose chromatography, and Sephadex gel chromatography; the homogeneity and the molecular weight of AP1-1 were determined by gel filtration; and the acid hydrolysis, periodate oxidation, Smith degradation, and NMR analysis were used to analyze the chemical structure of AP1-1.	DEAE-Cellulose	103-117	JunB proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	28-33