PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2605191-0	1989	Cholesterol metabolism by purified cytochrome P-450scc is highly stimulated by octyl glucoside and stearic acid exclusively in large unilamellar phospholipid vesicles.	octyl-beta-D-glucoside	79-94	cholesterol side-chain cleavage enzyme, mitochondrial	Bos taurus	35-54
2909509-2	1989	Cytochrome b558 was solubilized from the crude membrane fraction which was pretreated with both 1 M potassium phosphate buffer and 1% octyl glucoside at low ionic strength.	octyl-beta-D-glucoside	134-149	mitochondrially encoded cytochrome b	Homo sapiens	0-12
2768222-1	1989	Human microsomal dipeptidase (MDP, formerly referred to as dehydropeptidase-I or renal dipeptidase) [EC 3.4.13.11] was solubilized from the membrane fraction of kidney by treatment with octyl-beta-D-glucoside and purified by a procedure including ion exchange chromatography and affinity chromatography on cilastatin-immobilized Sepharose.	octyl-beta-D-glucoside	186-208	dipeptidase 1	Homo sapiens	6-28
2768222-1	1989	Human microsomal dipeptidase (MDP, formerly referred to as dehydropeptidase-I or renal dipeptidase) [EC 3.4.13.11] was solubilized from the membrane fraction of kidney by treatment with octyl-beta-D-glucoside and purified by a procedure including ion exchange chromatography and affinity chromatography on cilastatin-immobilized Sepharose.	octyl-beta-D-glucoside	186-208	dipeptidase 1	Homo sapiens	30-33
2768222-1	1989	Human microsomal dipeptidase (MDP, formerly referred to as dehydropeptidase-I or renal dipeptidase) [EC 3.4.13.11] was solubilized from the membrane fraction of kidney by treatment with octyl-beta-D-glucoside and purified by a procedure including ion exchange chromatography and affinity chromatography on cilastatin-immobilized Sepharose.	octyl-beta-D-glucoside	186-208	dipeptidase 1	Homo sapiens	59-77
2768222-1	1989	Human microsomal dipeptidase (MDP, formerly referred to as dehydropeptidase-I or renal dipeptidase) [EC 3.4.13.11] was solubilized from the membrane fraction of kidney by treatment with octyl-beta-D-glucoside and purified by a procedure including ion exchange chromatography and affinity chromatography on cilastatin-immobilized Sepharose.	octyl-beta-D-glucoside	186-208	dipeptidase 1	Homo sapiens	81-98
2465293-3	1989	When an octyl glucoside extract of surface-radioiodinated platelets was applied to an affinity matrix of KYGRGDS-coupled Sepharose 4B, a 160-kDa-labeled protein (P160) and GPIIb-IIIa bound and were specifically eluted by soluble GRGDSP peptide, but not by the variant GRGESP peptide.	octyl-beta-D-glucoside	8-23	MYB binding protein 1a	Homo sapiens	162-166
2465293-3	1989	When an octyl glucoside extract of surface-radioiodinated platelets was applied to an affinity matrix of KYGRGDS-coupled Sepharose 4B, a 160-kDa-labeled protein (P160) and GPIIb-IIIa bound and were specifically eluted by soluble GRGDSP peptide, but not by the variant GRGESP peptide.	octyl-beta-D-glucoside	8-23	integrin subunit alpha 2b	Homo sapiens	172-177
2470757-7	1989	The following observations suggest that the structure capable of recognizing Lex per se on F9 cells is Lex: (i) Cell surface-labeled components solubilized in octylglucoside, affinity-bound on an Lex-octyl-Sepharose column, contained glycoproteins reactive with anti-Lex antibody.	octyl-beta-D-glucoside	159-173	fucosyltransferase 4	Mus musculus	77-80
2470757-7	1989	The following observations suggest that the structure capable of recognizing Lex per se on F9 cells is Lex: (i) Cell surface-labeled components solubilized in octylglucoside, affinity-bound on an Lex-octyl-Sepharose column, contained glycoproteins reactive with anti-Lex antibody.	octyl-beta-D-glucoside	159-173	fucosyltransferase 4	Mus musculus	103-106
2470757-7	1989	The following observations suggest that the structure capable of recognizing Lex per se on F9 cells is Lex: (i) Cell surface-labeled components solubilized in octylglucoside, affinity-bound on an Lex-octyl-Sepharose column, contained glycoproteins reactive with anti-Lex antibody.	octyl-beta-D-glucoside	159-173	fucosyltransferase 4	Mus musculus	103-106
2470757-7	1989	The following observations suggest that the structure capable of recognizing Lex per se on F9 cells is Lex: (i) Cell surface-labeled components solubilized in octylglucoside, affinity-bound on an Lex-octyl-Sepharose column, contained glycoproteins reactive with anti-Lex antibody.	octyl-beta-D-glucoside	159-173	fucosyltransferase 4	Mus musculus	103-106
2541739-1	1989	Acid sphingomyelinase was purified to homogeneity from human placenta in the presence of a dialyzable detergent, n-octyl-beta-D-glucopyranoside.	octyl-beta-D-glucoside	113-143	sphingomyelin phosphodiesterase 1	Homo sapiens	0-21
2909509-3	1989	The solubilization of cytochrome b558 was carried out efficiently with 1.6% octyl glucoside in the presence of 100 mM phosphate buffer.	octyl-beta-D-glucoside	76-91	mitochondrially encoded cytochrome b	Homo sapiens	22-34
2846575-1	1988	The non-ionic detergent n-octyl-beta-D-glucopyranoside was used to solubilize the VIP (vasoactive intestinal peptide) receptor from human colonic adenocarcinoma cell line HT29-D4.	octyl-beta-D-glucoside	24-54	vasoactive intestinal peptide	Homo sapiens	82-85
2904677-2	1988	This NEM-sensitive ATPase was solubilized with n-octyl glucoside and purified using anion-exchange sievorptive chromatography on sequential DEAE-Sephadex and QAE-Sephadex columns followed by a final hydroxyapatite HPLC column.	octyl-beta-D-glucoside	47-64	dynein axonemal heavy chain 8	Homo sapiens	19-25
2846575-9	1988	When analyzed by gel filtration, the n-octyl-beta-D-glucopyranoside-solubilized 125I-VIP-receptor complex was resolved into two major peaks with molecular mass in the range of 60-70 and 270-300 kDa.	octyl-beta-D-glucoside	37-67	vasoactive intestinal peptide	Homo sapiens	85-88
3042032-3	1988	Sixty-seven to one hundred percent of the PH-20 antigenic activity present in an octylglucoside (OG) extract of sperm was recovered in the purified protein.	octyl-beta-D-glucoside	81-95	hyaluronidase PH-20	Cavia porcellus	42-47
3167081-1	1988	Phospholipase A has been solubilized from the sarcoplasmic reticulum of rat heart by treatment with Tris buffer, potassium chloride, taurodeoxycholate or octyl glucoside.	octyl-beta-D-glucoside	154-169	phospholipase A and acyltransferase 1	Rattus norvegicus	0-15
3164277-0	1988	High-performance liquid chromatography of the main polypeptide (MP26) of lens fiber plasma membranes solubilized with n-octyl beta-D-glucopyranoside.	octyl-beta-D-glucoside	118-148	major intrinsic protein of lens fiber	Homo sapiens	64-68
3372499-4	1988	Triton X-100, N-octyl-beta-D-glucopyranoside, and Zwittergent were effective in solubilizing PAM activity from crude pituitary membranes.	octyl-beta-D-glucoside	14-44	peptidylglycine alpha-amidating monooxygenase	Rattus norvegicus	93-96
3371459-9	1988	Total cellular LDL receptor-mediated binding, measured using an octylglucoside solubilization-filtration assay, confirmed the CF-induced decrease in high-affinity LDL binding.	octyl-beta-D-glucoside	64-78	low density lipoprotein receptor	Homo sapiens	15-27
2455298-3	1988	Two protocols were followed to purify the IFN-gamma receptor from octyl glucoside-solubilized membranes: (i) sequential affinity chromatography over wheat germ agglutinin- and IFN-gamma-Sepharose and (ii) affinity chromatography over columns containing receptor-specific monoclonal antibody and wheat germ agglutinin.	octyl-beta-D-glucoside	66-81	interferon gamma	Homo sapiens	42-51
3042032-3	1988	Sixty-seven to one hundred percent of the PH-20 antigenic activity present in an octylglucoside (OG) extract of sperm was recovered in the purified protein.	octyl-beta-D-glucoside	97-99	hyaluronidase PH-20	Cavia porcellus	42-47
3042032-4	1988	From 10(10) sperm, approximately 0.4 mg of PH-20 protein was obtained, which was about 0.24% of the total protein in the OG extract.	octyl-beta-D-glucoside	121-123	hyaluronidase PH-20	Cavia porcellus	43-48
3355850-4	1988	Human platelet phospholipase A2 was solubilized and then partially purified in the presence of n-octyl-beta-D-glucopyranoside (octyl glucoside).	octyl-beta-D-glucoside	95-125	phospholipase A2 group IB	Homo sapiens	15-31
2965731-6	1988	Liposomes prepared from octyl-beta-D-glucopyranoside-extracted YAC-1 and NK-enriched effector cell membranes interfered with conjugate formation, whereas liposomes prepared from NK-insensitive P815 cells were inconsequential.	octyl-beta-D-glucoside	24-52	ADP-ribosyltransferase 1	Mus musculus	63-68
3355850-4	1988	Human platelet phospholipase A2 was solubilized and then partially purified in the presence of n-octyl-beta-D-glucopyranoside (octyl glucoside).	octyl-beta-D-glucoside	127-142	phospholipase A2 group IB	Homo sapiens	15-31
3337799-2	1988	The hydrodynamic studies indicated that the cytochrome b/detergent complex had a sedimentation coefficient, partial specific volume and Stokes radius of 5.25 S, 0.82 cm3/g and 6.2 nm in Triton X-100 and 6.05 S, 0.80 cm3/g and 5.6 nm in octylglucoside, respectively.	octyl-beta-D-glucoside	236-250	mitochondrially encoded cytochrome b	Homo sapiens	44-56
3343241-4	1988	This phospholipase A2 has now been solubilized from the membrane fraction with octyl glucoside and partially purified.	octyl-beta-D-glucoside	79-94	phospholipase A2, group IB, pancreas	Mus musculus	5-21
2963631-3	1988	Iodinated recombinant mouse gamma interferon incubated with WEHI-3 cells, as well as membranes prepared from them, bound specifically to a single class of sites with a Kd of 7 x 10(-9)M. Membranes were solubilized with the non-ionic detergent octyl-beta-D-glucopyranoside.	octyl-beta-D-glucoside	243-271	interferon gamma	Mus musculus	28-44
3949762-5	1986	But when the particulate fraction was briefly sonicated in 0.1% octylglucoside before chromatography at 22 degrees C, a different PLA2 activity peak, specific for PtdCho, was obtained.	octyl-beta-D-glucoside	64-78	phospholipase A2 group IIA	Homo sapiens	130-134
3435484-2	1987	Phospholipase A2 was solubilized and partially purified to a stable form in the presence of n-octyl beta-D-glucopyranoside (octyl glucoside), and its enzymic activity was determined with sonicated 2.5 microM-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine (arachidonoyl-PC) as substrate.	octyl-beta-D-glucoside	92-122	phospholipase A2 group IB	Homo sapiens	0-16
3435484-2	1987	Phospholipase A2 was solubilized and partially purified to a stable form in the presence of n-octyl beta-D-glucopyranoside (octyl glucoside), and its enzymic activity was determined with sonicated 2.5 microM-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine (arachidonoyl-PC) as substrate.	octyl-beta-D-glucoside	124-139	phospholipase A2 group IB	Homo sapiens	0-16
2824466-5	1987	The apparent molecular weight of the 125I-VIP.receptor.detergent complex was calculated as 270,000 +/- 36,000 in Triton X-100 and 320,000 +/- 32,000 in n-octyl-beta-D-glucopyranoside.	octyl-beta-D-glucoside	152-182	vasoactive intestinal peptide	Rattus norvegicus	42-45
3300709-0	1987	The use of a monoclonal antibody for the rapid purification of kidney neutral endopeptidase ("enkephalinase") solubilized in octyl glucoside.	octyl-beta-D-glucoside	125-140	neprilysin	Oryctolagus cuniculus	94-108
3300709-2	1987	In contrast with other methods used so far, a complete extraction of enkephalinase from the brush border membrane can be achieved with octyl glucoside, without loss of activity.	octyl-beta-D-glucoside	135-150	neprilysin	Oryctolagus cuniculus	69-82
3023809-1	1986	The atrial natriuretic factor (ANF) receptor has been solubilized from bovine adrenal zona glomerulosa membranes with the nonionic detergent octyl-beta-D-glucoside.	octyl-beta-D-glucoside	141-163	natriuretic peptide A	Bos taurus	31-34
3756201-3	1986	In the presence of 24 mM n-octyl-beta-D-glucopyranoside (octylglucoside) phospholipase A2 was effectively (more than 90%) extracted from platelet lysates without solubilization of platelet membranes.	octyl-beta-D-glucoside	25-55	phospholipase A2 group IB	Homo sapiens	73-89
3756201-3	1986	In the presence of 24 mM n-octyl-beta-D-glucopyranoside (octylglucoside) phospholipase A2 was effectively (more than 90%) extracted from platelet lysates without solubilization of platelet membranes.	octyl-beta-D-glucoside	57-71	phospholipase A2 group IB	Homo sapiens	73-89
3768315-2	1986	By use of a mixed detergent system of cholate and octyl glucoside to solubilize the phospholipid and rhodopsin, 15 membrane complexes of predetermined phospholipid to rhodopsin mole ratios of between 350:1 and 65:1 have been produced by exhaustive dialysis and studied by a variety of techniques.	octyl-beta-D-glucoside	50-65	rhodopsin	Bos taurus	101-110
3768315-2	1986	By use of a mixed detergent system of cholate and octyl glucoside to solubilize the phospholipid and rhodopsin, 15 membrane complexes of predetermined phospholipid to rhodopsin mole ratios of between 350:1 and 65:1 have been produced by exhaustive dialysis and studied by a variety of techniques.	octyl-beta-D-glucoside	50-65	rhodopsin	Bos taurus	167-176
3956935-1	1986	Rat lingual lipase was purified to homogeneity by solubilization in 1% octylglucoside, followed by centrifugation, affinity chromatography on hydroxylapatite, gel filtration, and chromatofocusing.	octyl-beta-D-glucoside	71-85	lipase F, gastric type	Rattus norvegicus	4-18
3597441-15	1987	Disruption of the mitochondrial inner membrane by octyl glucoside causes inactivation of carnitine palmitoyltransferase I while releasing carnitine palmitoyltransferase II in active form.	octyl-beta-D-glucoside	50-65	carnitine palmitoyltransferase 2	Rattus norvegicus	138-171
3597442-3	1987	Exposure of rat liver mitochondrial membranes to octyl glucoside, Triton X-100, or Tween 20 solubilized an active and tetradecylglycidyl-CoA (TG-CoA)-insensitive carnitine palmitoyltransferase (presumed to be carnitine palmitoyltransferase II).	octyl-beta-D-glucoside	49-64	carnitine palmitoyltransferase 2	Rattus norvegicus	209-242
3654814-5	1987	The apparent Mr values for the octyl glucoside complexes of the main components were: anion transporter, 900,000; glycophorin A, 210,000-360,000, dependent on ionic strength; glucose transporter, 110,000-160,000; lipids, 70,000.	octyl-beta-D-glucoside	31-46	glycophorin A (MNS blood group)	Homo sapiens	114-127
3566971-5	1987	As with the other nonionic detergents examined, Triton X-100 and octyl beta-D-glucoside were maximally effective in solubilizing acetylcholinesterase activity at concentrations greater than their respective critical micelle concentrations.	octyl-beta-D-glucoside	65-87	acetylcholinesterase	Bos taurus	129-149
2876988-0	1986	Reconstitution of mitochondrial F0.F1-ATPase with phosphatidylcholine using the nonionic detergent, octylglucoside.	octyl-beta-D-glucoside	100-114	ATP synthase F1 subunit epsilon	Homo sapiens	32-44
2876989-1	1986	Beef heart mitochondrial F0.F1-ATPase was reconstituted into phospholipid liposomes using the octylglucoside solubilization, discontinuous sucrose gradient centrifugation procedure described in the preceding manuscript (Laird, D., Smith Eble, K., and Cunningham, C. (1986) J. Biol.	octyl-beta-D-glucoside	94-108	ATP synthase F1 subunit epsilon	Homo sapiens	25-37
4041439-1	1985	Spectral changes accompanying the binding of the nonionic detergent n-octyl beta-D-glucopyranoside (n-octyl glucoside) to cytochrome P-450LM2 purified from liver microsomes of phenobarbital-treated rabbits have been compared to changes in catalytic activity obtained in a reconstituted system consisting of various levels of detergent, P-450LM2, and NADPH-cytochrome P-450 reductase.	octyl-beta-D-glucoside	68-98	cytochrome P450 2B4	Oryctolagus cuniculus	122-141
3002479-2	1986	The stability of porin structure in solution is much higher in the presence of beta-octyl glucoside than with SDS.	octyl-beta-D-glucoside	79-99	voltage dependent anion channel 1	Homo sapiens	17-22
3002479-4	1986	The nonionic detergent, beta-octyl glucoside, increases the stability of porin in acidic conditions, since neither dissociation nor denaturation was observed in the pH region between 7.5 and 2.0.	octyl-beta-D-glucoside	24-44	voltage dependent anion channel 1	Homo sapiens	73-78
3002479-6	1986	The thermal stability of porin is also increased by beta-octyl glucoside as evidenced by a transition temperature 15-20 degrees C higher as compared to SDS.	octyl-beta-D-glucoside	52-72	voltage dependent anion channel 1	Homo sapiens	25-30
3002479-7	1986	A considerable degree of native porin structure was regained after heat treatment in the presence of beta-octyl glucoside, though the reconstituted trimers were not identical to the native ones.	octyl-beta-D-glucoside	101-121	voltage dependent anion channel 1	Homo sapiens	32-37
3957415-2	1986	On western blots of lymphocyte surface proteins which had been solubilized and electrophoretically separated in octylglucoside, they detected bands which comigrated with Ly-6A.2 or Ly-6E.1 antigens.	octyl-beta-D-glucoside	112-126	lymphocyte antigen 6 complex, locus A	Mus musculus	170-177
3957415-2	1986	On western blots of lymphocyte surface proteins which had been solubilized and electrophoretically separated in octylglucoside, they detected bands which comigrated with Ly-6A.2 or Ly-6E.1 antigens.	octyl-beta-D-glucoside	112-126	lymphocyte antigen 6 complex, locus A	Mus musculus	181-188
2422138-3	1986	After different detergent treatments, with either octyl glucoside or sodium N-lauroyl sarcosinate, SAF showed differing sedimentation characteristics but nevertheless cosedimented with scrapie infectivity in both cases.	octyl-beta-D-glucoside	50-65	phosphatidylglycerophosphate synthase 1	Mus musculus	99-102
4074733-2	1985	The procedure relies on the ability of the hydrophobic resin Bio-Beads SM-2 to remove octyl glucoside from a mixture of deoxycholate-purified bR, asolectin, and the detergent.	octyl-beta-D-glucoside	86-101	SM2	Homo sapiens	71-75
3933557-1	1985	Carnitine acylcarnitine translocase has been solubilized from inverted inner membrane vesicles of rat liver mitochondria with octyl glucoside and reconstituted into asolectin liposomes.	octyl-beta-D-glucoside	126-141	solute carrier family 25 member 20	Rattus norvegicus	0-35
4041439-1	1985	Spectral changes accompanying the binding of the nonionic detergent n-octyl beta-D-glucopyranoside (n-octyl glucoside) to cytochrome P-450LM2 purified from liver microsomes of phenobarbital-treated rabbits have been compared to changes in catalytic activity obtained in a reconstituted system consisting of various levels of detergent, P-450LM2, and NADPH-cytochrome P-450 reductase.	octyl-beta-D-glucoside	68-98	cytochrome P450 2B4	Oryctolagus cuniculus	133-141
4041439-1	1985	Spectral changes accompanying the binding of the nonionic detergent n-octyl beta-D-glucopyranoside (n-octyl glucoside) to cytochrome P-450LM2 purified from liver microsomes of phenobarbital-treated rabbits have been compared to changes in catalytic activity obtained in a reconstituted system consisting of various levels of detergent, P-450LM2, and NADPH-cytochrome P-450 reductase.	octyl-beta-D-glucoside	68-98	NADPH--cytochrome P450 reductase	Oryctolagus cuniculus	350-382
4041439-1	1985	Spectral changes accompanying the binding of the nonionic detergent n-octyl beta-D-glucopyranoside (n-octyl glucoside) to cytochrome P-450LM2 purified from liver microsomes of phenobarbital-treated rabbits have been compared to changes in catalytic activity obtained in a reconstituted system consisting of various levels of detergent, P-450LM2, and NADPH-cytochrome P-450 reductase.	octyl-beta-D-glucoside	100-117	cytochrome P450 2B4	Oryctolagus cuniculus	122-141
4041439-1	1985	Spectral changes accompanying the binding of the nonionic detergent n-octyl beta-D-glucopyranoside (n-octyl glucoside) to cytochrome P-450LM2 purified from liver microsomes of phenobarbital-treated rabbits have been compared to changes in catalytic activity obtained in a reconstituted system consisting of various levels of detergent, P-450LM2, and NADPH-cytochrome P-450 reductase.	octyl-beta-D-glucoside	100-117	cytochrome P450 2B4	Oryctolagus cuniculus	133-141
4041439-1	1985	Spectral changes accompanying the binding of the nonionic detergent n-octyl beta-D-glucopyranoside (n-octyl glucoside) to cytochrome P-450LM2 purified from liver microsomes of phenobarbital-treated rabbits have been compared to changes in catalytic activity obtained in a reconstituted system consisting of various levels of detergent, P-450LM2, and NADPH-cytochrome P-450 reductase.	octyl-beta-D-glucoside	100-117	NADPH--cytochrome P450 reductase	Oryctolagus cuniculus	350-382
4078886-1	1985	Purified, delipidated rhodopsin is recombined with phospholipid using octyl-glucoside (OG) and preformed vesicles.	octyl-beta-D-glucoside	70-85	rhodopsin	Bos taurus	22-31
2859892-2	1985	The pig small intestinal dipeptidyl peptidase IV was asymmetrically integrated into egg phosphatidylcholine and microvillar lipid vesicles prepared by a beta-octylglucoside dialysis method.	octyl-beta-D-glucoside	153-172	dipeptidyl peptidase 4	Sus scrofa	25-48
4078886-1	1985	Purified, delipidated rhodopsin is recombined with phospholipid using octyl-glucoside (OG) and preformed vesicles.	octyl-beta-D-glucoside	87-89	rhodopsin	Bos taurus	22-31
6233283-1	1984	A Ca2+-ATPase from human platelets has been purified after solubilization with octyl glucoside.	octyl-beta-D-glucoside	79-94	dynein axonemal heavy chain 8	Homo sapiens	7-13
3881128-0	1985	Rhodopsin-egg phosphatidylcholine reconstitution by an octyl glucoside dilution procedure.	octyl-beta-D-glucoside	55-70	rhodopsin	Bos taurus	0-9
3881128-1	1985	The transmembrane protein bovine rhodopsin was reconstituted with egg phosphatidylcholine (PC) by using a modified detergent dilution technique employing the nonionic detergent octyl-beta-D-glucoside (octyl glucoside).	octyl-beta-D-glucoside	177-199	rhodopsin	Bos taurus	33-42
3881128-1	1985	The transmembrane protein bovine rhodopsin was reconstituted with egg phosphatidylcholine (PC) by using a modified detergent dilution technique employing the nonionic detergent octyl-beta-D-glucoside (octyl glucoside).	octyl-beta-D-glucoside	201-216	rhodopsin	Bos taurus	33-42
6704207-1	1984	Cytochrome P-450 and NADPH cytochrome P-450 reductase were incorporated into large unilamellar lipid vesicles (200-300 nm in diameter) removing octylglucoside from mixed micelles by dialysis.	octyl-beta-D-glucoside	144-158	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	0-53
6421812-1	1984	Sedimentation equilibrium experiments with NADPH-cytochrome P-450 reductase showed that increasing 1-O-n-octyl-beta-D-glucopyranoside levels promoted disaggregation of the flavoprotein.	octyl-beta-D-glucoside	99-133	cytochrome p450 oxidoreductase	Homo sapiens	43-75
6704207-0	1984	Incorporation of the cytochrome P-450 monooxygenase system into large unilamellar liposomes using octylglucoside, especially for measurements of protein diffusion in membranes.	octyl-beta-D-glucoside	98-112	cytochrome P450 family 20 subfamily A member 1	Homo sapiens	21-51
6225641-12	1983	Activation of a Mg-specific ATPase in CF1 by octyl glucoside decreases the affinity for ADP and inorganic phosphate by about threefold but increases the affinity for ATP.	octyl-beta-D-glucoside	45-60	dynein axonemal heavy chain 8	Homo sapiens	28-34
6662111-1	1983	A cytochrome b-f complex has been extracted from pea chloroplast membranes with octyl glucoside and cholate and has been purified by ammonium sulphate fractionation and polyacrylamide gel electrophoresis in the presence of Triton X-100 and sodium deoxycholate.	octyl-beta-D-glucoside	80-95	mitochondrially encoded cytochrome b	Homo sapiens	2-14
6603574-5	1983	About 70% of H-2Kb activity could be eluted from anti-H-2Kb-immunoadsorbents in the presence of 3 M NH4SCN and octyl glucoside (pH 7.4).	octyl-beta-D-glucoside	111-126	histocompatibility 2, K1, K region	Mus musculus	13-18
6603574-5	1983	About 70% of H-2Kb activity could be eluted from anti-H-2Kb-immunoadsorbents in the presence of 3 M NH4SCN and octyl glucoside (pH 7.4).	octyl-beta-D-glucoside	111-126	histocompatibility 2, K1, K region	Mus musculus	54-59
6830759-5	1983	Fluorescent-labeled rhodopsin was affinity purified in octyl glucoside from rod outer segments which were previously reacted with either the sulfhydryl-specific reagents, pyrenylmaleimide or monobromobimane, or reagents specific to amino groups, dansyl chloride or fluorescein isothiocyanate.	octyl-beta-D-glucoside	55-70	rhodopsin	Homo sapiens	20-29
6184373-2	1983	Binding sites having the characteristics of receptors for "activated" alpha 2-macroglobulin (alpha 2M) have been solubilized with octyl-beta-D-glucoside from fibroblast membranes.	octyl-beta-D-glucoside	130-152	alpha-2-macroglobulin	Mus musculus	70-91
6184373-2	1983	Binding sites having the characteristics of receptors for "activated" alpha 2-macroglobulin (alpha 2M) have been solubilized with octyl-beta-D-glucoside from fibroblast membranes.	octyl-beta-D-glucoside	130-152	alpha-2-macroglobulin	Mus musculus	93-101
6298234-1	1983	The receptor for nerve growth factor (NGF) has been purified to near homogeneity from octylglucoside extracts of A875 melanoma cell membranes by the use of repetitive affinity chromatography on NGF-Sepharose.	octyl-beta-D-glucoside	86-100	nerve growth factor	Homo sapiens	17-36
6298234-1	1983	The receptor for nerve growth factor (NGF) has been purified to near homogeneity from octylglucoside extracts of A875 melanoma cell membranes by the use of repetitive affinity chromatography on NGF-Sepharose.	octyl-beta-D-glucoside	86-100	nerve growth factor	Homo sapiens	38-41
6298234-2	1983	Elution of purified receptor (NGF receptor) was accomplished with 0.15 M NaCl, pH 11.0, containing phosphatidylcholine and octylglucoside.	octyl-beta-D-glucoside	123-137	nerve growth factor receptor	Homo sapiens	30-42
6830760-3	1983	The interactions between rhodopsin molecules in a micellar detergent solution (octyl glucoside) and in reconstituted phospholipid vesicles were studied in the dark and after bleaching.	octyl-beta-D-glucoside	79-94	rhodopsin	Homo sapiens	25-34
6816797-6	1982	Sedimentation equilibrium experiments with P-450LM2 alone or in the presence of equimolar reductase showed that increasing octylglucoside levels promoted disaggregation of the cytochrome.	octyl-beta-D-glucoside	123-137	cytochrome P450 2B4	Oryctolagus cuniculus	43-51
6816797-9	1982	Moreover, both gel filtration and sedimentation equilibrium experiments demonstrated that a stable complex between P-450LM2 and its reductase was not formed at octylglucoside concentrations where high activity was evident.	octyl-beta-D-glucoside	160-174	cytochrome P450 2B4	Oryctolagus cuniculus	115-123
6816797-1	1982	The detergent 1-O-n-octyl-beta-D-glucopyranoside (octylglucoside) was found to replace the phospholipid requirement in the demethylation of benzphetamine by cytochrome P-450LM2 and NADPH-cytochrome P-450 reductase purified from phenobarbital-treated rabbit liver.	octyl-beta-D-glucoside	14-48	cytochrome P450 2B4	Oryctolagus cuniculus	157-176
7171574-0	1982	Rhodopsin-phospholipid reconstitution by dialysis removal of octyl glucoside.	octyl-beta-D-glucoside	61-76	rhodopsin	Homo sapiens	0-9
6816797-1	1982	The detergent 1-O-n-octyl-beta-D-glucopyranoside (octylglucoside) was found to replace the phospholipid requirement in the demethylation of benzphetamine by cytochrome P-450LM2 and NADPH-cytochrome P-450 reductase purified from phenobarbital-treated rabbit liver.	octyl-beta-D-glucoside	14-48	NADPH--cytochrome P450 reductase	Oryctolagus cuniculus	181-213
6816797-1	1982	The detergent 1-O-n-octyl-beta-D-glucopyranoside (octylglucoside) was found to replace the phospholipid requirement in the demethylation of benzphetamine by cytochrome P-450LM2 and NADPH-cytochrome P-450 reductase purified from phenobarbital-treated rabbit liver.	octyl-beta-D-glucoside	50-64	cytochrome P450 2B4	Oryctolagus cuniculus	157-176
6816797-1	1982	The detergent 1-O-n-octyl-beta-D-glucopyranoside (octylglucoside) was found to replace the phospholipid requirement in the demethylation of benzphetamine by cytochrome P-450LM2 and NADPH-cytochrome P-450 reductase purified from phenobarbital-treated rabbit liver.	octyl-beta-D-glucoside	50-64	NADPH--cytochrome P450 reductase	Oryctolagus cuniculus	181-213
6979541-1	1982	The hydrogen exchange behavior of rhodopsin was re-examined by studies of the protein in the disc membrane and after solubilization in octyl glucoside.	octyl-beta-D-glucoside	135-150	rhodopsin	Homo sapiens	34-43
7096323-1	1982	Cytochrome b561 from bovine adrenal medulla chromaffin granules was purified in octylglucoside by hydrophobic chromatography.	octyl-beta-D-glucoside	80-94	cytochrome b561	Bos taurus	0-15
19431520-0	1982	Rhodopsin-Phospholipid Reconstitution from Octyl Glucoside-solubilized Samples.	octyl-beta-D-glucoside	43-58	rhodopsin	Homo sapiens	0-9
6254970-1	1980	The low density lipoprotein (LDL) receptor has been solubilized from bovine adrenocortical membranes with octyl-beta-D-glucoside and purified 350-fold in the presence of the detergent.	octyl-beta-D-glucoside	106-128	low density lipoprotein receptor	Bos taurus	4-42
7213599-1	1981	Solubilization of retinal rod outer segment disk membranes in octyl glucoside was employed to prepare rhodopsin samples with varying amounts of associated disk phospholipid.	octyl-beta-D-glucoside	62-77	rhodopsin	Homo sapiens	102-111
7213639-1	1980	At least two components of neuraminidase (acylneuraminyl hydrolase, EC 3.2.1.18) can be distinguished in human leucocytes on the basis of pH optimum, thermolability at 30 degrees C and the effect of the detergent octyl-beta-D-glucoside.	octyl-beta-D-glucoside	213-235	neuraminidase 1	Homo sapiens	27-40
6121556-2	1981	Pig intestinal microvillus aminopeptidase (EC 3.4.11.2) was reincorporated into lipid membranes by using either beta-octyl glucoside or sodium deoxycholate.	octyl-beta-D-glucoside	112-132	alanyl aminopeptidase, membrane	Sus scrofa	27-41
230482-1	1979	The low density lipoprotein (LDL) receptor was solubilized from membranes of bovine adrenal cortex and cultured human cells by incubation with the nonionic detergent octyl-beta-D-glucoside.	octyl-beta-D-glucoside	166-188	low density lipoprotein receptor	Bos taurus	4-42
7400149-1	1980	Highly purified HLA (A and B) antigens in octylglucoside were quantitatively incorporated into egg lecithin vesicles, and it was demonstrated that vesicles of different densities could be prepared by varying the ratio of lipid to protein.	octyl-beta-D-glucoside	42-56	major histocompatibility complex, class I, A	Homo sapiens	16-28
16661309-1	1980	The K(+)-stimulated ATPase was partially purified from a plasma membrane fraction from corn roots (WF9 x Mo 17) by solubilization with 30 millimolar octyl-beta-d-glucopyranoside followed by precipitation with dilute ammonium sulfate.	octyl-beta-D-glucoside	149-177	ATPase	Zea mays	20-26
16661309-9	1980	Low concentrations of each detergent, including octyl-beta-d-glucopyranoside, activated the ATPase and higher concentrations inactivated the enzyme.	octyl-beta-D-glucoside	48-76	ATPase	Zea mays	92-98
230482-7	1979	While in the soluble form in the presence of octyl-beta-D-glucoside, the LDL receptor can be carried through several steps of purification.	octyl-beta-D-glucoside	45-67	low density lipoprotein receptor	Homo sapiens	73-85
549635-4	1979	Octyl glucoside preferentially extracts aminopeptidase M and gamma-glutamyltranspeptidase in a concentration-dependent manner.	octyl-beta-D-glucoside	0-15	alanyl aminopeptidase, membrane	Homo sapiens	40-56
31758269-5	2019	After magnetic separation of the composites and adding n-octyl-beta-D-glucopyranoside, the fluorophore sulforhodamine B (SRB) is released.	octyl-beta-D-glucoside	55-85	chaperonin containing TCP1 subunit 4	Homo sapiens	103-119
456344-2	1979	The binding isotherms of bovine serum albumin with octylglucoside and decyl glucoside were determined at 7 degrees C and 25 degrees C at pH 7.4 and ionic strength 0.1 M. The average number of detergent molecules bound was found to increase with increasing hydrocarbon chain length.	octyl-beta-D-glucoside	51-65	albumin	Homo sapiens	32-45
397058-1	1979	The insulin receptor was solubilized from turkey erythrocyte membranes by extraction with 1% beta-octylglucopyranoside.	octyl-beta-D-glucoside	93-118	insulin receptor	Meleagris gallopavo	4-20
33345726-0	2020	Targeting a conserved pocket (n-octyl-beta-D-glucoside) on the dengue virus envelope protein by small bioactive molecule inhibitors.	octyl-beta-D-glucoside	30-54	endogenous retrovirus group K member 6, envelope	Homo sapiens	76-92
31758269-5	2019	After magnetic separation of the composites and adding n-octyl-beta-D-glucopyranoside, the fluorophore sulforhodamine B (SRB) is released.	octyl-beta-D-glucoside	55-85	chaperonin containing TCP1 subunit 4	Homo sapiens	121-124
31521813-5	2019	The release profile of VEGF-LLC was controlled using octyl glucoside (OG) as a hydration-modulating agent, which could enlarge the water channel, yielding a 2-fold increase in water channel size and a 7-fold increase in VEGF release.	octyl-beta-D-glucoside	53-68	vascular endothelial growth factor A	Homo sapiens	23-27
31521813-5	2019	The release profile of VEGF-LLC was controlled using octyl glucoside (OG) as a hydration-modulating agent, which could enlarge the water channel, yielding a 2-fold increase in water channel size and a 7-fold increase in VEGF release.	octyl-beta-D-glucoside	70-72	vascular endothelial growth factor A	Homo sapiens	23-27
31521813-14	2019	The results showed that the addition of octyl glucoside (OG) could change the water channel size of LLC, which enabled the LLC system to release VEGF in a sustained manner and to possess a suitable modulus to favor angiogenesis simultaneously.	octyl-beta-D-glucoside	40-55	vascular endothelial growth factor A	Rattus norvegicus	145-149
31521813-14	2019	The results showed that the addition of octyl glucoside (OG) could change the water channel size of LLC, which enabled the LLC system to release VEGF in a sustained manner and to possess a suitable modulus to favor angiogenesis simultaneously.	octyl-beta-D-glucoside	57-59	vascular endothelial growth factor A	Rattus norvegicus	145-149
28836172-7	2018	OG treatment can inhibit the expression of TNF-alpha and IL-6.	octyl-beta-D-glucoside	0-2	tumor necrosis factor	Rattus norvegicus	43-52
31667125-6	2019	Here we describe a simple method that dissociates ACAT1 dimers through the addition of the non-ionic detergents Triton X-100 or octyl glucoside which disrupt the C-terminal dimerization domain.	octyl-beta-D-glucoside	128-143	acetyl-CoA acetyltransferase 1	Homo sapiens	50-55
31251920-0	2019	Triton X-100 or octyl glucoside inactivates acyl-CoA:cholesterol acyltransferase 1 by dissociating it from a two-fold dimer to a two-fold monomer.	octyl-beta-D-glucoside	16-31	acetyl-CoA acetyltransferase 1	Homo sapiens	44-82
31251920-10	2019	Here we show that treating ACAT1 with non-ionic detergent, Triton X-100 or octyl glucoside, causes the enzyme to become a two-fold monomer without any enzymatic activity.	octyl-beta-D-glucoside	75-90	acetyl-CoA acetyltransferase 1	Homo sapiens	27-32
29942142-10	2018	OG administration potentiated this effect and increased the NLR value, which was blocked by GSH, suggesting that reactive oxygen species play a critical role in maintaining lymphocyte numbers.	octyl-beta-D-glucoside	0-2	C-X-C motif chemokine receptor 5	Rattus norvegicus	60-63
31667125-8	2019	This method can be applied to dissociate ACAT1 subunits by using Triton X-100 or octyl glucoside.	octyl-beta-D-glucoside	81-96	acetyl-CoA acetyltransferase 1	Homo sapiens	41-46
31496649-11	2019	Inhibition of Wnt/beta-catenin by ICG-001 significantly reversed the effect of OG on osteogenic and adipogenic differentiation of BMSCs.	octyl-beta-D-glucoside	79-81	catenin beta 1	Homo sapiens	18-30
30851394-7	2019	Three detergents (1,2-diheptanoyol-sn-glycero-3-phosphocholine, dodecyl maltoside and n-octyl-beta-d-glucopyranoside) were used to solubilize and purify P-gp from insect cell membranes.	octyl-beta-D-glucoside	86-116	ATP binding cassette subfamily B member 1	Homo sapiens	153-157
28836172-7	2018	OG treatment can inhibit the expression of TNF-alpha and IL-6.	octyl-beta-D-glucoside	0-2	interleukin 6	Rattus norvegicus	57-61
29500903-3	2018	When octyl-beta-d-glucopyranoside is used to reconstitute the protein, Syt1 is present in an aggregated state that is mediated by the long juxta-membrane linker.	octyl-beta-D-glucoside	5-33	synaptotagmin 1	Homo sapiens	71-75
29415006-0	2018	A single beta-octyl glucoside molecule induces HIV-1 Nef dimer formation in the absence of partner protein binding.	octyl-beta-D-glucoside	9-29	Nef	Human immunodeficiency virus 1	53-56
29664970-0	2018	Correction: A single beta-octyl glucoside molecule induces HIV-1 Nef dimer formation in the absence of partner protein binding.	octyl-beta-D-glucoside	21-41	Nef	Human immunodeficiency virus 1	65-68
28326898-7	2018	Under these conditions, the mean removal of OG from synthesized solution after 720 minutes of treatment was 86.64% (59.51 mg L-1) for the electroflotation process and 61.52% (12.91 mg L-1) after down-flow granular filtration.	octyl-beta-D-glucoside	44-46	immunoglobulin kappa variable 1-16	Homo sapiens	125-128
28326898-7	2018	Under these conditions, the mean removal of OG from synthesized solution after 720 minutes of treatment was 86.64% (59.51 mg L-1) for the electroflotation process and 61.52% (12.91 mg L-1) after down-flow granular filtration.	octyl-beta-D-glucoside	44-46	immunoglobulin kappa variable 1-16	Homo sapiens	184-187
29415006-6	2018	In this study, we show that monomeric Nef core proteins can be induced to form dimers in the presence of low concentrations of the non-ionic surfactant, beta-octyl glucoside (betaOG).	octyl-beta-D-glucoside	153-173	S100 calcium binding protein B	Homo sapiens	38-41
28259683-1	2017	Olumacostat glasaretil (OG) is a small molecule inhibitor of acetyl coenzyme A (CoA) carboxylase (ACC), the enzyme that controls the first rate-limiting step in fatty acid biosynthesis.	octyl-beta-D-glucoside	24-26	acetyl-CoA carboxylase alpha	Homo sapiens	98-101
29110486-4	2018	We found that mAb 1A5 could immunoprecipitate Cad11 when membranes were solubilized by dodecyl maltoside (DDM) but not by octylglucoside, suggesting that octylglucoside interferes with Cad11-mAb 1A5 interaction.	octyl-beta-D-glucoside	154-168	cadherin 11	Homo sapiens	46-51
29110486-4	2018	We found that mAb 1A5 could immunoprecipitate Cad11 when membranes were solubilized by dodecyl maltoside (DDM) but not by octylglucoside, suggesting that octylglucoside interferes with Cad11-mAb 1A5 interaction.	octyl-beta-D-glucoside	154-168	cadherin 11	Homo sapiens	185-190
29211991-4	2017	Assessment of the method"s precision and robustness is evaluated by performing shape restorations from simulated data of a tetrameric alpha-helical membrane channel (Aquaporin-0) solubilized by n-Dodecyl beta-D-Maltoside and from previously published small-angle neutron scattering experimental data of the filamentous hemagglutinin adhesin beta-barrel protein transporter solubilized by n-Octyl beta-D-glucopyranoside.	octyl-beta-D-glucoside	388-418	major intrinsic protein of lens fiber	Homo sapiens	166-177
29629142-7	2018	The model reveals that OG originates from stimulated emission from the bi-exciton states and the OG threshold is reached when the average number of excitons per NPL is about half the occupation of the band-edge exciton states.	octyl-beta-D-glucoside	23-25	N-acetylneuraminate pyruvate lyase	Homo sapiens	161-164
24196960-5	2013	UCP1 was folded in octyl glucoside, as indicated by its high helical content and binding to ATP, a known UCP1 proton transport inhibitor.	octyl-beta-D-glucoside	19-34	uncoupling protein 1	Homo sapiens	0-4
27792324-5	2016	In contrast, A2AR mutants in either octylglucoside or nonylglucoside showed decreased alpha-helicity in transmembrane regions, decreased alpha-helical packing, and the interpenetration of detergent molecules between transmembrane alpha-helices.	octyl-beta-D-glucoside	36-50	adenosine A2a receptor	Homo sapiens	13-17
25907854-4	2015	The alpha-helix content of Apo A-1 increased from 50% in aqueous buffer to 75% in the presence of lipid vesicles, but remained constant in solutions of beta-octyl glucoside.	octyl-beta-D-glucoside	152-172	apolipoprotein A1	Homo sapiens	27-34
24338013-3	2014	We report the effects of N-terminal acetylation on alpha-synuclein binding to lipid vesicles of different composition and curvature and to micelles composed of the detergents beta-octyl-glucoside (BOG) and SDS.	octyl-beta-D-glucoside	175-195	synuclein alpha	Homo sapiens	51-66
23838013-9	2014	Our findings suggest that OG improved depressive behaviour in CUMS rats by downregulating HPA axis hyperactivity and increasing BDNF expression and ERK1/2 phosphorylation in the hippocampus.	octyl-beta-D-glucoside	26-28	brain-derived neurotrophic factor	Rattus norvegicus	128-132
23838013-9	2014	Our findings suggest that OG improved depressive behaviour in CUMS rats by downregulating HPA axis hyperactivity and increasing BDNF expression and ERK1/2 phosphorylation in the hippocampus.	octyl-beta-D-glucoside	26-28	mitogen activated protein kinase 3	Rattus norvegicus	148-154
26696140-4	2016	We identified 2",7"-dichlorofluorescein (DCF), 4",5"-dibromofluorescein (DBF), and Oregon green (OG) as good OATP1B1 substrates with Km values of 5.29, 4.16, and 54.1 muM and Vmax values of 87.9, 48.1, and 187 pmol/min/mg protein, respectively.	octyl-beta-D-glucoside	97-99	solute carrier organic anion transporter family member 1B1	Homo sapiens	109-116
26696140-4	2016	We identified 2",7"-dichlorofluorescein (DCF), 4",5"-dibromofluorescein (DBF), and Oregon green (OG) as good OATP1B1 substrates with Km values of 5.29, 4.16, and 54.1 muM and Vmax values of 87.9, 48.1, and 187 pmol/min/mg protein, respectively.	octyl-beta-D-glucoside	97-99	latexin	Homo sapiens	167-170
26696140-5	2016	In addition to FL, fluo-3, and 8-fluorescein-cAMP, OG, and DBF were identified as OATP1B3 substrates.	octyl-beta-D-glucoside	51-53	solute carrier organic anion transporter family member 1B3	Homo sapiens	82-89
26696140-6	2016	FL, OG, DCF, and DBF were identified as OATP2B1 substrates.	octyl-beta-D-glucoside	4-6	solute carrier organic anion transporter family member 2B1	Homo sapiens	40-47
24312215-3	2013	We have investigated the thermal stress-induced structural alterations of detergent (octyl glucoside)-solubilized calf lens AQP0.	octyl-beta-D-glucoside	85-100	major intrinsic protein of lens fiber	Bos taurus	124-128
23948376-3	2013	To reveal new mechanisms modulating prion conversion, we analyzed the PrP(C) profiles by determining the differential PrP(C) protein solubilities in the anionic and nonionic detergents N-lauroylsarcosine, N-octyl-beta-D-glucopyranoside, CHAPS and deoxycholic acid.	octyl-beta-D-glucoside	205-235	prion protein	Homo sapiens	70-76
24196960-5	2013	UCP1 was folded in octyl glucoside, as indicated by its high helical content and binding to ATP, a known UCP1 proton transport inhibitor.	octyl-beta-D-glucoside	19-34	uncoupling protein 1	Homo sapiens	105-109
23772395-4	2013	CPT-2 is a monotopic membrane protein and was solubilized by beta-octylglucoside (beta-OG) above its critical micellar concentration (CMC) to perform inhibitor titrations in solutions containing detergent micelles.	octyl-beta-D-glucoside	61-80	carnitine palmitoyltransferase 2	Rattus norvegicus	0-5
23611728-3	2013	The LDT-mediated labeling yielded a semisynthetic FKBP12 containing the Oregon green (OG) dye near the catalytic pocket.	octyl-beta-D-glucoside	86-88	FKBP prolyl isomerase 1A	Homo sapiens	50-56
23772395-4	2013	CPT-2 is a monotopic membrane protein and was solubilized by beta-octylglucoside (beta-OG) above its critical micellar concentration (CMC) to perform inhibitor titrations in solutions containing detergent micelles.	octyl-beta-D-glucoside	82-89	carnitine palmitoyltransferase 2	Rattus norvegicus	0-5
16470026-3	2006	Purified PGHS-1 was stabilized when solubilized in beta-octylglucoside (rather than Tween-20 or CHAPS) and when reconstituted with hemin chloride (rather than hematin).	octyl-beta-D-glucoside	51-70	prostaglandin-endoperoxide synthase 1	Homo sapiens	9-15
20804539-6	2010	However, even when a comparable number of B cells were present in the mesentery, the absence of TNFalpha resulted in similar defects in OG formation after pristane treatment, demonstrating that both B cells and TNFalpha are very crucial for pristane-induced OG formation.	octyl-beta-D-glucoside	136-138	tumor necrosis factor	Mus musculus	96-104
20804539-6	2010	However, even when a comparable number of B cells were present in the mesentery, the absence of TNFalpha resulted in similar defects in OG formation after pristane treatment, demonstrating that both B cells and TNFalpha are very crucial for pristane-induced OG formation.	octyl-beta-D-glucoside	258-260	tumor necrosis factor	Mus musculus	211-219
20045406-6	2010	Therefore, we developed an optimized purification method based on n-octyl-beta-d-glucopyranoside solubilization, where the functional properties of beta(2)-adrenoceptor, Gs and adenylate cyclase were preserved in the CRLDF.	octyl-beta-D-glucoside	66-96	adrenoceptor beta 2	Homo sapiens	148-168
19664589-0	2010	Dissimilar mechanisms of cytochrome c release induced by octyl glucoside-activated BAX and by BAX activated with truncated BID.	octyl-beta-D-glucoside	57-72	cytochrome c, somatic	Homo sapiens	25-37
19664589-0	2010	Dissimilar mechanisms of cytochrome c release induced by octyl glucoside-activated BAX and by BAX activated with truncated BID.	octyl-beta-D-glucoside	57-72	BCL2 associated X, apoptosis regulator	Homo sapiens	83-86
19564333-5	2009	During BAX activation with n-octyl glucoside, it has been shown that BAX forms high molecular weight complexes that are larger than the combined molecular weight of BAX monomer and one detergent micelle.	octyl-beta-D-glucoside	27-44	BCL2 associated X, apoptosis regulator	Homo sapiens	7-10
19564333-5	2009	During BAX activation with n-octyl glucoside, it has been shown that BAX forms high molecular weight complexes that are larger than the combined molecular weight of BAX monomer and one detergent micelle.	octyl-beta-D-glucoside	27-44	BCL2 associated X, apoptosis regulator	Homo sapiens	69-72
19564333-5	2009	During BAX activation with n-octyl glucoside, it has been shown that BAX forms high molecular weight complexes that are larger than the combined molecular weight of BAX monomer and one detergent micelle.	octyl-beta-D-glucoside	27-44	BCL2 associated X, apoptosis regulator	Homo sapiens	69-72
19811221-6	2009	In the presence of the specific fatty acid amide hydrolase (FAAH) inhibitors URB597 and AM374, though, 2-OG hydrolysis was inhibited up to 55% in a concentration-dependent manner (IC(50) = 129.8 nM and 20.9 nM respectively).	octyl-beta-D-glucoside	105-107	fatty acid amide hydrolase	Homo sapiens	32-58
19811221-6	2009	In the presence of the specific fatty acid amide hydrolase (FAAH) inhibitors URB597 and AM374, though, 2-OG hydrolysis was inhibited up to 55% in a concentration-dependent manner (IC(50) = 129.8 nM and 20.9 nM respectively).	octyl-beta-D-glucoside	105-107	fatty acid amide hydrolase	Homo sapiens	60-64
17194147-8	2007	Subsequently, the SRB dye molecules were released from the bound liposomes via the addition of the detergent octyl glucopyranoside.	octyl-beta-D-glucoside	109-130	chaperonin containing TCP1 subunit 4	Homo sapiens	18-21
17098868-6	2006	These peptide surfactants not only enhance the stability of bovine rhodopsin in the presence of lipids and the common surfactants n-dodecyl-beta-D-maltoside and octyl-D-glucoside, but they also significantly stabilize rhodopsin under thermal denaturation conditions, even after lipids are removed.	octyl-beta-D-glucoside	161-178	rhodopsin	Bos taurus	67-76
23201117-4	2013	As this GPI-linked receptor predominantly resides in lipid rafts (LR), we used a modified RIPA lysis buffer containing the non-ionic detergent, octyl-glucoside which solubilizes LRs to extract uPAR.	octyl-beta-D-glucoside	144-159	plasminogen activator, urokinase receptor	Homo sapiens	193-197
21515882-3	2011	Rat liver microsomal lysoplasmalogenase was solubilized with octyl glucoside and purified 500-fold to near homogeneity using four chromatography steps.	octyl-beta-D-glucoside	61-76	transmembrane protein 86B	Homo sapiens	21-39
21689528-3	2011	Rhodopsin kinetic stability was examined under subsolubilizing (rhodopsin in a bilayer environment perturbed by octyl-beta-D-glucopyranoside) and under fully solubilizing conditions (rhodopsin in a micelle with cosolubilized phospholipids).	octyl-beta-D-glucoside	112-140	rhodopsin	Bos taurus	0-9
21560112-7	2011	The proinflammatory cytokines IL1-beta and TNF-alpha significantly increased the expression of CTGF (p<0.05) by 65.1% and 101.3%, respectively, and the expression and secretion of OGP by 62.3-165.8% (p<0.05).	octyl-beta-D-glucoside	183-186	interleukin 1 beta	Homo sapiens	30-38
21560112-7	2011	The proinflammatory cytokines IL1-beta and TNF-alpha significantly increased the expression of CTGF (p<0.05) by 65.1% and 101.3%, respectively, and the expression and secretion of OGP by 62.3-165.8% (p<0.05).	octyl-beta-D-glucoside	183-186	tumor necrosis factor	Homo sapiens	43-52
21070768-6	2011	Single and sequential application of the detergents Triton X-100, octyl-glucopyranoside and CHAPS facilitated high solubility of glycosylated PrP(C) isoforms, whereas high proportions of nonglycosylated PrP(C) remained non-soluble.	octyl-beta-D-glucoside	66-87	prion protein	Homo sapiens	142-148
19307590-0	2009	Binding of an octylglucoside detergent molecule in the second substrate (S2) site of LeuT establishes an inhibitor-bound conformation.	octyl-beta-D-glucoside	14-28	Leucine transport, high	Homo sapiens	85-89
19307590-3	2009	Here, we show a profound inhibitory effect of n-octyl-beta-d-glucopyranoside (OG), the detergent used for LeuT crystallization, on substrate binding to the S2 site.	octyl-beta-D-glucoside	46-76	Leucine transport, high	Homo sapiens	106-110
19307590-3	2009	Here, we show a profound inhibitory effect of n-octyl-beta-d-glucopyranoside (OG), the detergent used for LeuT crystallization, on substrate binding to the S2 site.	octyl-beta-D-glucoside	78-80	Leucine transport, high	Homo sapiens	106-110
19307590-6	2009	We also observed electron density at the S2 site in LeuT-WT crystals, and this also was accounted for by an OG molecule in that site.	octyl-beta-D-glucoside	108-110	Leucine transport, high	Homo sapiens	52-56
18841885-1	2008	We report on photophysical studies of the interaction between an anesthetic analogue, methyl 2-amino-4,5-dimethoxybenzoate (ADMB), with the human serum albumin (HSA) protein and the normal micelle of n-octyl-beta-D-glucopyranoside (OG) in water solutions.	octyl-beta-D-glucoside	232-234	albumin	Homo sapiens	146-173
17996248-6	2008	Since Cyt b could be affinity-purified in the detergent octylglucoside, high-level functional reconstitution was carried out directly on elution fractions by simple addition of solubilized phospholipid and subsequent dialysis for detergent removal.	octyl-beta-D-glucoside	56-70	mitochondrially encoded cytochrome b	Homo sapiens	6-11
17266258-11	2007	Reasonable agreement between the CMCs predicted by the CS-MT model and the experimental CMCs was obtained for octyl glucoside (OG), dodecyl maltoside (DM), octyl sulfinyl ethanol (OSE), decyl methyl sulfoxide (C10SO), decyl dimethyl phosphine oxide (C10PO), and decanoyl-n-methylglucamide (MEGA-10).	octyl-beta-D-glucoside	110-125	chorionic somatomammotropin hormone 1	Homo sapiens	55-60
17266258-11	2007	Reasonable agreement between the CMCs predicted by the CS-MT model and the experimental CMCs was obtained for octyl glucoside (OG), dodecyl maltoside (DM), octyl sulfinyl ethanol (OSE), decyl methyl sulfoxide (C10SO), decyl dimethyl phosphine oxide (C10PO), and decanoyl-n-methylglucamide (MEGA-10).	octyl-beta-D-glucoside	127-129	chorionic somatomammotropin hormone 1	Homo sapiens	55-60
16729976-7	2006	However, perturbation of the lipid environment of the reconstituted Pgp by nonionic detergent octylglucoside abolishes stimulation by cis-(Z)-flupentixol of [125I]IAAP binding.	octyl-beta-D-glucoside	94-108	phosphoglycolate phosphatase	Homo sapiens	68-71
16800634-4	2006	GLUT1 forms a multimeric complex in octyl glucoside that dissociates upon addition of reductant.	octyl-beta-D-glucoside	36-51	solute carrier family 2 member 1	Homo sapiens	0-5
16042397-8	2005	DGKA displayed Michaelis-Menten kinetics with respect to bulk substrate concentration (1,2-dioleoyl-sn-glycerol) in octyl glucoside mixed micelles when the surface substrate concentration was at or below 3.5 mol %.	octyl-beta-D-glucoside	116-131	diacylglycerol kinase alpha	Homo sapiens	0-4
16596723-8	2006	RESULTS: The levels of Akt protein expression increased significantly after partial hepatectomy in OG group and with a peak at 24 h post operation.	octyl-beta-D-glucoside	99-101	AKT serine/threonine kinase 1	Rattus norvegicus	23-26
16849006-0	2006	Permeability enhancing effects of the alkylglycoside, octylglucoside, on insulin permeation across epithelial membrane in vitro.	octyl-beta-D-glucoside	54-68	insulin	Homo sapiens	73-80
16849006-1	2006	PURPOSE: To evaluate the permeability enhancing effects of octylglucoside (OG) for molecules with poor absorption such as insulin by in vitro cell models.	octyl-beta-D-glucoside	59-73	insulin	Homo sapiens	122-129
16849006-1	2006	PURPOSE: To evaluate the permeability enhancing effects of octylglucoside (OG) for molecules with poor absorption such as insulin by in vitro cell models.	octyl-beta-D-glucoside	75-77	insulin	Homo sapiens	122-129
16309179-1	2005	Membrane vesicles from the multidrug-resistant KB-V1 and KB-C1 cell lines overexpressing P-glycoprotein (Pgp), responsible for pleiotropic chemotherapeutic agents resistance, were solubilized with octyl-glucoside (OG-EX) and further fractionated on DEAE-sepharose column with increased concentrations of NaCl.	octyl-beta-D-glucoside	197-212	ATP binding cassette subfamily B member 1	Homo sapiens	105-108
15501933-3	2005	Octylglucoside-solubilized rhodopsin was incorporated by detergent dilution into solid-supported bilayers composed either of egg phosphatidylcholine or various mixtures of a nonlamellar-forming lipid (dioleoylphosphatidylethanolamine; DOPE) together with a lamellar-forming lipid (dioleoylphosphatidylcholine; DOPC).	octyl-beta-D-glucoside	0-14	rhodopsin	Homo sapiens	27-36
16096722-1	2005	The in vitro reassembled species of OmpF porin, which was renatured from its denatured monomer using n-octyl-beta-D-glucopyranoside, was characterized by low-angle laser light scattering photometry, circular dichroism spectroscopy and synchrotron radiation small-angle X-ray scattering measurements.	octyl-beta-D-glucoside	101-131	voltage dependent anion channel 1	Homo sapiens	41-46
14687727-0	2003	Determination of CD59 protein in normal human serum by enzyme immunoassay, using octyl-glucoside detergent to release glycosyl-phosphatidylinositol-CD59 from lipid complex.	octyl-beta-D-glucoside	81-96	CD59 molecule (CD59 blood group)	Homo sapiens	17-21
15265584-4	2004	Salt (1.0M NaCl), but not non-ionic detergents such as Triton X-100 (1.0%) and n-octyl glucoside (1.0%), could dissociate eEF1A from the PSD core.	octyl-beta-D-glucoside	79-96	eukaryotic translation elongation factor 1 alpha 1	Rattus norvegicus	122-127
15240890-9	2004	NHE1 in Chinese hamster ovary fibroblasts (but not NHE3 in opossum kidney cells) is inhibited by agents that thin the membrane (L-alpha-lysophosphatidylcholine and octyl-beta-D-glucopyranoside) and activated by cholesterol enrichment, which thickens membranes.	octyl-beta-D-glucoside	164-192	sodium/hydrogen exchanger 1	Cricetulus griseus	0-4
15293782-3	2004	Five proteins are abundant in a caveolin-1 protein complex, analyzed by sucrose gradient velocity sedimentation following octyl-beta-D-glucopyranoside extraction.	octyl-beta-D-glucoside	122-150	caveolin 1	Homo sapiens	32-42
16328826-2	2004	A peripheral observation towards the end of 1979 initiated an intensive investigation, which is still ongoing today: next to the ATP synthase the cytochrome b (6f ) complex could be selectively solubilized from the chloroplast membrane by the combined action of octyl glucoside and cholate.	octyl-beta-D-glucoside	262-277	mitochondrially encoded cytochrome b	Homo sapiens	146-158
14690423-1	2003	Membrane-bound H/K-ATPase was solubilized by octaethylene glycol dodecyl ether (C(12)E(8)) or n-octyl glucoside (nOG).	octyl-beta-D-glucoside	94-111	ATPase H+/K+ transporting subunit alpha	Sus scrofa	15-25
14687727-0	2003	Determination of CD59 protein in normal human serum by enzyme immunoassay, using octyl-glucoside detergent to release glycosyl-phosphatidylinositol-CD59 from lipid complex.	octyl-beta-D-glucoside	81-96	CD59 molecule (CD59 blood group)	Homo sapiens	148-152
12684054-5	2003	Sodium deoxycholate (SDC) and octyl-beta-glucoside (OG), structurally similar to CHAPS and Brij35 and disrupting the lipid bilayer, showed a modest increase of MRP1 photolabeling with IAARh123.	octyl-beta-D-glucoside	52-54	ATP binding cassette subfamily C member 1	Homo sapiens	160-164
12269810-7	2002	We report structures of human apolipoprotein A-II and its complex with beta-octyl glucoside, a widely used lipid surrogate.	octyl-beta-D-glucoside	71-91	apolipoprotein A2	Homo sapiens	30-49
12460774-2	2002	The mPGES-1 was solubilized from Sf9 cell membranes with diheptanoylphosphatidylcholine and purified in the presence of octylglucoside using hydroxyapatite column chromatography.	octyl-beta-D-glucoside	120-134	prostaglandin E synthase	Mus musculus	4-11
12747626-7	2003	RESULTS: The incubation of paraffin sections with ICG-sulfo-OSu-labeled MUC1 antibody resulted in positive staining of the tumor sites by an IR fluorescence imaging system, and the intensity of fluorescence was increased depending on the concentration of octylglucoside and grade of imaging processing.	octyl-beta-D-glucoside	255-269	mucin 1, cell surface associated	Homo sapiens	72-76
12202484-7	2002	Consistent with cytoskeletal association, most DRM-H-associated flotillin 2, Lyn, and Galpha(i-2) also resist extraction with 0.1 m octyl glucoside.	octyl-beta-D-glucoside	132-147	flotillin 2	Bos taurus	64-75
12202484-7	2002	Consistent with cytoskeletal association, most DRM-H-associated flotillin 2, Lyn, and Galpha(i-2) also resist extraction with 0.1 m octyl glucoside.	octyl-beta-D-glucoside	132-147	LYN proto-oncogene, Src family tyrosine kinase	Bos taurus	77-80
12269810-9	2002	Dramatic changes, observed in the presence of beta-octyl glucoside, might provide clues to the structural basis for its antagonism of apolipoprotein A-I.	octyl-beta-D-glucoside	46-66	apolipoprotein A1	Homo sapiens	134-152
12200375-6	2002	Furthermore, the C-terminal CA domain of N-WASp, which sequesters Arp2/3 complex, inhibits by half the actin nucleation capacity of octylglucoside-permeabilized and activated WAS platelets, similar to its effect in WASp-expressing cells.	octyl-beta-D-glucoside	132-146	WASP like actin nucleation promoting factor	Homo sapiens	41-47
12370420-2	2002	Rhodopsin purified from rod outer segments of bovine retinae by immunoaffinity chromatography in octyl glucoside was reconstituted into liposomes prepared from soybean phospholipids by detergent dialysis.	octyl-beta-D-glucoside	97-112	rhodopsin	Bos taurus	0-9
12200375-6	2002	Furthermore, the C-terminal CA domain of N-WASp, which sequesters Arp2/3 complex, inhibits by half the actin nucleation capacity of octylglucoside-permeabilized and activated WAS platelets, similar to its effect in WASp-expressing cells.	octyl-beta-D-glucoside	132-146	actin related protein 2	Homo sapiens	66-70
12200375-6	2002	Furthermore, the C-terminal CA domain of N-WASp, which sequesters Arp2/3 complex, inhibits by half the actin nucleation capacity of octylglucoside-permeabilized and activated WAS platelets, similar to its effect in WASp-expressing cells.	octyl-beta-D-glucoside	132-146	WASP actin nucleation promoting factor	Homo sapiens	43-46
12200375-6	2002	Furthermore, the C-terminal CA domain of N-WASp, which sequesters Arp2/3 complex, inhibits by half the actin nucleation capacity of octylglucoside-permeabilized and activated WAS platelets, similar to its effect in WASp-expressing cells.	octyl-beta-D-glucoside	132-146	WASP actin nucleation promoting factor	Homo sapiens	43-47
12186385-1	2002	The refolding and reassembly of an integral membrane protein OmpF porin denatured in sodium dodecylsulfate (SDS) into its stable species by the addition of n-octyl-beta-D-glucopyranoside (OG) have been studied by means of circular dichroism (CD) spectroscopy and low-angle laser light scattering photometry coupled with high-performance gel chromatography.	octyl-beta-D-glucoside	156-186	voltage dependent anion channel 1	Homo sapiens	66-71
12186385-1	2002	The refolding and reassembly of an integral membrane protein OmpF porin denatured in sodium dodecylsulfate (SDS) into its stable species by the addition of n-octyl-beta-D-glucopyranoside (OG) have been studied by means of circular dichroism (CD) spectroscopy and low-angle laser light scattering photometry coupled with high-performance gel chromatography.	octyl-beta-D-glucoside	188-190	voltage dependent anion channel 1	Homo sapiens	66-71
11910014-6	2002	Gel filtration of microsomal fractions solubilized with octylglucoside revealed that the Cf-9 protein, either as c-myc or TAP fusions, migrated at a molecular mass of 350 to 475 kD.	octyl-beta-D-glucoside	56-70	Carbohydrate-binding protein	Arabidopsis thaliana	89-93
11855827-4	2002	In contrast to the ZAP-70/diphosphorylated CD8-epsilon-ITAM interaction, the Lck/monophosphorylated CD8-epsilon-ITAM interaction was sensitive to octylglucoside, an agent that disrupts Lck interaction with membrane rafts.	octyl-beta-D-glucoside	146-160	LCK proto-oncogene, Src family tyrosine kinase	Homo sapiens	77-80
11855827-4	2002	In contrast to the ZAP-70/diphosphorylated CD8-epsilon-ITAM interaction, the Lck/monophosphorylated CD8-epsilon-ITAM interaction was sensitive to octylglucoside, an agent that disrupts Lck interaction with membrane rafts.	octyl-beta-D-glucoside	146-160	CD8a molecule	Homo sapiens	100-103
11855827-4	2002	In contrast to the ZAP-70/diphosphorylated CD8-epsilon-ITAM interaction, the Lck/monophosphorylated CD8-epsilon-ITAM interaction was sensitive to octylglucoside, an agent that disrupts Lck interaction with membrane rafts.	octyl-beta-D-glucoside	146-160	LCK proto-oncogene, Src family tyrosine kinase	Homo sapiens	185-188
11861064-5	2002	HIV-1IHI Env, expressed on the surface of Rabbit Kidney cells (RK13) with a recombinant vaccinia virus (rVV), was solubilized using the non-ionic detergent n-Octyl beta-D-glucopyranoside (OG).	octyl-beta-D-glucoside	156-186	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	0-12
11861064-5	2002	HIV-1IHI Env, expressed on the surface of Rabbit Kidney cells (RK13) with a recombinant vaccinia virus (rVV), was solubilized using the non-ionic detergent n-Octyl beta-D-glucopyranoside (OG).	octyl-beta-D-glucoside	188-190	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	0-12
11413134-7	2001	Analytical ultracentrifugation experiments revealed that SLN oligomerizes in the presence of the nonionic detergents octylpolyoxyethylene and octyl glucoside in a concentration-dependent manner.	octyl-beta-D-glucoside	142-157	sarcolipin	Homo sapiens	57-60
11686930-0	2001	Octyl glucoside induced formation of the molten globule-like state of glutamate dehydrogenase.	octyl-beta-D-glucoside	0-15	glutamate dehydrogenase 1, mitochondrial	Bos taurus	70-93
11686930-1	2001	The interaction between n-octyl-beta-D-glucopyranoside (octyl glucoside) and bovine liver glutamate dehydrogenase (GDH) was studied using techniques including equilibrium dialysis, UV-spectrophotometry, circular dichroism (CD), fluorescence energy transfer and extrinsic spectrofluorometry in 50 mM sodium phosphate buffer solution (pH 7.6).	octyl-beta-D-glucoside	24-54	glutamate dehydrogenase 1, mitochondrial	Bos taurus	90-113
11686930-1	2001	The interaction between n-octyl-beta-D-glucopyranoside (octyl glucoside) and bovine liver glutamate dehydrogenase (GDH) was studied using techniques including equilibrium dialysis, UV-spectrophotometry, circular dichroism (CD), fluorescence energy transfer and extrinsic spectrofluorometry in 50 mM sodium phosphate buffer solution (pH 7.6).	octyl-beta-D-glucoside	24-54	glutamate dehydrogenase 1, mitochondrial	Bos taurus	115-118
11686930-1	2001	The interaction between n-octyl-beta-D-glucopyranoside (octyl glucoside) and bovine liver glutamate dehydrogenase (GDH) was studied using techniques including equilibrium dialysis, UV-spectrophotometry, circular dichroism (CD), fluorescence energy transfer and extrinsic spectrofluorometry in 50 mM sodium phosphate buffer solution (pH 7.6).	octyl-beta-D-glucoside	56-71	glutamate dehydrogenase 1, mitochondrial	Bos taurus	90-113
11686930-1	2001	The interaction between n-octyl-beta-D-glucopyranoside (octyl glucoside) and bovine liver glutamate dehydrogenase (GDH) was studied using techniques including equilibrium dialysis, UV-spectrophotometry, circular dichroism (CD), fluorescence energy transfer and extrinsic spectrofluorometry in 50 mM sodium phosphate buffer solution (pH 7.6).	octyl-beta-D-glucoside	56-71	glutamate dehydrogenase 1, mitochondrial	Bos taurus	115-118
11686930-2	2001	The equilibrium dialysis experiment showed a higher binding of octyl glucoside to GDH that induces up to 80% enzyme inhibition in 20 mM octyl glucoside solution.	octyl-beta-D-glucoside	63-78	glutamate dehydrogenase 1, mitochondrial	Bos taurus	82-85
11686930-2	2001	The equilibrium dialysis experiment showed a higher binding of octyl glucoside to GDH that induces up to 80% enzyme inhibition in 20 mM octyl glucoside solution.	octyl-beta-D-glucoside	136-151	glutamate dehydrogenase 1, mitochondrial	Bos taurus	82-85
11686930-3	2001	The CD study indicated that GDH retains its secondary structure in the presence of octyl glucoside, but loses a degree of its tertiary structure by acquiring a more extended tertiary structure.	octyl-beta-D-glucoside	83-98	glutamate dehydrogenase 1, mitochondrial	Bos taurus	28-31
11686930-4	2001	Measurement of the binding of a hydrophobic fluorescent probe, 1-anilino-naphthalene-8-sulfonate (ANS), to GDH revealed that the binding of ANS to GDH is increased in the presence of octyl glucoside, a finding that may be interpreted in terms of the increment of surface hydrophobic patch(es) of GDH because of its binding to octyl glucoside.	octyl-beta-D-glucoside	183-198	glutamate dehydrogenase 1, mitochondrial	Bos taurus	107-110
11686930-4	2001	Measurement of the binding of a hydrophobic fluorescent probe, 1-anilino-naphthalene-8-sulfonate (ANS), to GDH revealed that the binding of ANS to GDH is increased in the presence of octyl glucoside, a finding that may be interpreted in terms of the increment of surface hydrophobic patch(es) of GDH because of its binding to octyl glucoside.	octyl-beta-D-glucoside	183-198	glutamate dehydrogenase 1, mitochondrial	Bos taurus	147-150
11686930-4	2001	Measurement of the binding of a hydrophobic fluorescent probe, 1-anilino-naphthalene-8-sulfonate (ANS), to GDH revealed that the binding of ANS to GDH is increased in the presence of octyl glucoside, a finding that may be interpreted in terms of the increment of surface hydrophobic patch(es) of GDH because of its binding to octyl glucoside.	octyl-beta-D-glucoside	183-198	glutamate dehydrogenase 1, mitochondrial	Bos taurus	147-150
11686930-4	2001	Measurement of the binding of a hydrophobic fluorescent probe, 1-anilino-naphthalene-8-sulfonate (ANS), to GDH revealed that the binding of ANS to GDH is increased in the presence of octyl glucoside, a finding that may be interpreted in terms of the increment of surface hydrophobic patch(es) of GDH because of its binding to octyl glucoside.	octyl-beta-D-glucoside	326-341	glutamate dehydrogenase 1, mitochondrial	Bos taurus	107-110
11686930-4	2001	Measurement of the binding of a hydrophobic fluorescent probe, 1-anilino-naphthalene-8-sulfonate (ANS), to GDH revealed that the binding of ANS to GDH is increased in the presence of octyl glucoside, a finding that may be interpreted in terms of the increment of surface hydrophobic patch(es) of GDH because of its binding to octyl glucoside.	octyl-beta-D-glucoside	326-341	glutamate dehydrogenase 1, mitochondrial	Bos taurus	147-150
11686930-4	2001	Measurement of the binding of a hydrophobic fluorescent probe, 1-anilino-naphthalene-8-sulfonate (ANS), to GDH revealed that the binding of ANS to GDH is increased in the presence of octyl glucoside, a finding that may be interpreted in terms of the increment of surface hydrophobic patch(es) of GDH because of its binding to octyl glucoside.	octyl-beta-D-glucoside	326-341	glutamate dehydrogenase 1, mitochondrial	Bos taurus	147-150
11686930-5	2001	Fluorescence energy transfer studies also showed more binding of the reduced coenzyme (NADH) to GDH and the Lineweaver-Burk plots (with respect to NADH) indicate the existence of substrate inhibition in the presence of octyl glucoside.	octyl-beta-D-glucoside	219-234	glutamate dehydrogenase 1, mitochondrial	Bos taurus	96-99
11686930-6	2001	These observations are aimed at explaining the formation of the molten globule-like structure of GDH, which is induced by a non-ionic detergent such as octyl glucoside.	octyl-beta-D-glucoside	152-167	glutamate dehydrogenase 1, mitochondrial	Bos taurus	97-100
11504728-4	2001	The Dol-P-P phosphatase encoded by CWH8 is optimally active in the presence of 0.5% octyl glucoside and relatively unstable in Triton X-100, distinguishing this activity from the lipid phosphatases encoded by LPP1 and DPP1.	octyl-beta-D-glucoside	84-99	dolichyldiphosphatase	Saccharomyces cerevisiae S288C	35-39
11811064-2	2001	Octyl beta-D-galactopyranoside and octyl beta-D-glucopyranoside were synthesized from the corresponding sugars (lactose or glucose) and octyl alcohol under catalysis with glycolytic enzymes, beta-galactosidase and beta-glucosidase, respectively.	octyl-beta-D-glucoside	35-63	galactosidase beta 1	Homo sapiens	191-209
10833273-5	2000	The preparation solubilized using n-octyl-beta-D-glucopyranoside from microsomes of CYP 4F2-expressing yeast cells catalyzes v- hydroxylation of LTB(4), 6-trans-LTB(4), lipoxin A(4), 8-hydroxyeicosatetraenoate, 12-hydroxyeicosatetraenoate, and 12-hydroxystearate in the presence of rabbit liver NADPH-P450 reductase.	octyl-beta-D-glucoside	34-64	cytochrome P450 family 4 subfamily F member 2	Homo sapiens	84-91
11256943-4	2001	When uroplakins are solubilized with 2% octylglucoside and fractionated with ion exchangers, UPIa and UPII were bound as a complex by a cation exchanger, whereas UPIb and UPIII were bound by an anion exchanger.	octyl-beta-D-glucoside	40-54	uroplakin 1A	Homo sapiens	93-97
11028547-6	2000	SP-A was purified from isolated surfactant using sequential butanol and octyl glucoside extractions.	octyl-beta-D-glucoside	72-87	surfactant protein A1	Homo sapiens	0-4
11074455-4	2000	The caveolin-1 in the membrane fraction extractable with 2% octyl glucoside was significant reduced, compared to untransformed cells.	octyl-beta-D-glucoside	60-75	caveolin 1	Homo sapiens	4-14
10614785-7	1999	When resting neutrophils were lysed in Triton X-100 or octyl glucoside buffer and separated into detergent-soluble and detergent-insoluble fractions, p40phox and p67phox were mainly associated with the detergent-insoluble fraction (defined as the cytoskeleton), whereas p47phox was mainly found in the soluble fraction.	octyl-beta-D-glucoside	55-70	neutrophil cytosolic factor 4	Homo sapiens	150-157
10644848-7	2000	If the binding of sialylated macromolecules was prevented by neuraminidase treatment, the parental virus was as sensitive to octylglucoside as were the HAD mutants.	octyl-beta-D-glucoside	125-139	neuraminidase 1	Homo sapiens	61-74
10620504-7	2000	Incubation of the monomeric Bax with 2% octyl glucoside induced formation of oligomers that displayed channel-forming activity in liposomes and triggered cytochrome c release from mitochondria.	octyl-beta-D-glucoside	40-55	BCL2 associated X, apoptosis regulator	Homo sapiens	28-31
10620504-7	2000	Incubation of the monomeric Bax with 2% octyl glucoside induced formation of oligomers that displayed channel-forming activity in liposomes and triggered cytochrome c release from mitochondria.	octyl-beta-D-glucoside	40-55	cytochrome c, somatic	Homo sapiens	154-166
10614785-7	1999	When resting neutrophils were lysed in Triton X-100 or octyl glucoside buffer and separated into detergent-soluble and detergent-insoluble fractions, p40phox and p67phox were mainly associated with the detergent-insoluble fraction (defined as the cytoskeleton), whereas p47phox was mainly found in the soluble fraction.	octyl-beta-D-glucoside	55-70	neutrophil cytosolic factor 2	Homo sapiens	162-169
10208569-4	1999	VDAC1 was enriched in the PSD fraction and was partially soluble in 1% n-octyl glucoside (NOG) or Triton X-100.	octyl-beta-D-glucoside	71-88	voltage-dependent anion channel 1	Rattus norvegicus	0-5
10620504-9	2000	In cytosolic extracts from mouse liver, Bax migrated at a molecular mass of 24000 Da on gel filtration, whereas after incubation of the cytosol with 2% octyl glucoside Bax migrated at approximately 140000 Da.	octyl-beta-D-glucoside	152-167	BCL2-associated X protein	Mus musculus	168-171
10231318-3	1999	METHODS: The distribution of intracellular IL-5 in human peripheral blood eosinophils (PBE) and lymphocytes (PBL) has been investigated using fixation and cell membrane permeabilization with octyl-glucopyranoside, the FOG-method, and flow cytometry.	octyl-beta-D-glucoside	191-212	interleukin 5	Homo sapiens	43-47
10198363-5	1999	Incubation of SP-A or SP-D with polymyxin, 100 mM N-octyl-beta-D-glucopyranoside, and 2 mM EDTA followed by dialysis was the most effective method of those tested for reducing endotoxin levels.	octyl-beta-D-glucoside	50-80	surfactant protein A1	Rattus norvegicus	14-18
10198363-5	1999	Incubation of SP-A or SP-D with polymyxin, 100 mM N-octyl-beta-D-glucopyranoside, and 2 mM EDTA followed by dialysis was the most effective method of those tested for reducing endotoxin levels.	octyl-beta-D-glucoside	50-80	surfactant protein D	Rattus norvegicus	22-26
10413522-1	1999	Rotational diffusion measurements using EPR and saturation transfer EPR were applied to analyze complex formation between the electron-transfer components of the mitochondrial steroid-hydroxylating cytochrome P450 systems (CYP11A1 and CYP11B1) in phosphatidylcholine/phosphatidylethanolamine/cardiolipin vesicles prepared by octyl glucoside dialysis/adsorption.	octyl-beta-D-glucoside	325-340	cytochrome P450 family 11 subfamily A member 1	Homo sapiens	223-230
10413522-1	1999	Rotational diffusion measurements using EPR and saturation transfer EPR were applied to analyze complex formation between the electron-transfer components of the mitochondrial steroid-hydroxylating cytochrome P450 systems (CYP11A1 and CYP11B1) in phosphatidylcholine/phosphatidylethanolamine/cardiolipin vesicles prepared by octyl glucoside dialysis/adsorption.	octyl-beta-D-glucoside	325-340	cytochrome P450 family 11 subfamily B member 1	Homo sapiens	235-242
10413522-2	1999	Octyl glucoside reconstitution of P450SCC results in large vesicles, which have an advantage over small vesicles in that vesicle tumbling does not contribute to measured rotational diffusion rates.	octyl-beta-D-glucoside	0-15	cytochrome P450 family 11 subfamily A member 1	Homo sapiens	34-41
9774337-9	1998	Significantly, LPA promoted the release of gelsolin from barbed actin filaments in octylglucoside-permeabilized human platelets.	octyl-beta-D-glucoside	83-97	gelsolin	Homo sapiens	43-51
10024463-7	1999	The rP5 was purified with the Talon metal affinity resin in a denatured form and then refolded by incorporation into mixed-detergent micelles of octylglucoside and SDS.	octyl-beta-D-glucoside	145-159	protein disulfide isomerase family A, member 6	Rattus norvegicus	4-7
9623777-1	1998	The glucose transporter of human erythrocytes (Glut1) was reconstituted into soybean phospholipid liposomes by a method of direct incorporation using the nonionic detergent n-octyl beta-D-glucopyranoside.	octyl-beta-D-glucoside	173-203	solute carrier family 2 member 1	Homo sapiens	47-52
9691283-5	1998	The catalytic activity of DAGK in detergents having medium-length alkyl chains such as dodecylphosphocholine or decylmaltoside was usually observed to be substantially higher than in short-chain detergents such as octylphosphocholine or octylglucoside.	octyl-beta-D-glucoside	237-251	diacylglycerol kinase alpha	Homo sapiens	26-30
9417990-1	1997	Aquaporin-1 (AQP-1) or CHIP28 occurs in glycosylated (glyCHIP) and non-glycosylated (CHIP) forms and solubilization in octyl-beta-D-glucoside (OG) results in a tight association of glyCHIP and CHIP to form a heterodimer.	octyl-beta-D-glucoside	143-145	aquaporin 1 (Colton blood group)	Homo sapiens	0-11
9338601-11	1997	Octylglucoside or Triton X-100 extracts of ascidian eggs had two forms of phospholipase activity as shown by ion affinity chromatography: PL1 eluting at 0.25 mol/L NaCl and PL2 eluting at 0.6 mol/L NaCl.	octyl-beta-D-glucoside	0-14	lethal, Chr 9, Russell 1	Mus musculus	138-141
9338601-11	1997	Octylglucoside or Triton X-100 extracts of ascidian eggs had two forms of phospholipase activity as shown by ion affinity chromatography: PL1 eluting at 0.25 mol/L NaCl and PL2 eluting at 0.6 mol/L NaCl.	octyl-beta-D-glucoside	0-14	lethal, Chr 9, Russell 2	Mus musculus	173-176
9538246-1	1998	Human glycosyl phosphatidylinositol-anchored protein CD59 was solubilized in detergent-insoluble complexes (DICs) and in post-nuclear pellets by a two-step solubilization procedure using Triton X-100 and octylglucoside.	octyl-beta-D-glucoside	204-218	CD59 molecule (CD59 blood group)	Homo sapiens	53-57
9417990-1	1997	Aquaporin-1 (AQP-1) or CHIP28 occurs in glycosylated (glyCHIP) and non-glycosylated (CHIP) forms and solubilization in octyl-beta-D-glucoside (OG) results in a tight association of glyCHIP and CHIP to form a heterodimer.	octyl-beta-D-glucoside	143-145	aquaporin 1 (Colton blood group)	Homo sapiens	13-18
9417990-1	1997	Aquaporin-1 (AQP-1) or CHIP28 occurs in glycosylated (glyCHIP) and non-glycosylated (CHIP) forms and solubilization in octyl-beta-D-glucoside (OG) results in a tight association of glyCHIP and CHIP to form a heterodimer.	octyl-beta-D-glucoside	143-145	aquaporin 1 (Colton blood group)	Homo sapiens	23-29
9042955-8	1997	The DAP was found to be contained in the sarcoglycan fraction which was prepared by treatment of the dystrophin-DAP complex with n-octyl beta-D-glucoside and crosslinked with beta- and/or gamma-sarcoglycan by a chemical crosslinker, dithiobis(succinimidyl propionate).	octyl-beta-D-glucoside	129-153	death associated protein	Homo sapiens	4-7
9310371-8	1997	On the other hand, ligand-bound [H57-H62, G63-G65]ET(B)R could be purified in various detergents, such as n-octyl-beta-D-glucopyranoside or n-decyl-beta-D-maltopyranoside.	octyl-beta-D-glucoside	106-136	endothelin receptor type B	Homo sapiens	50-56
9237635-5	1997	We have shown that about 66% of the annexin 2 associated with the Triton-X100-insoluble fraction is soluble in octylglucoside while the remnants are insoluble in the detergent and remain likely associated with actin filaments and associated cytoskeleton proteins.	octyl-beta-D-glucoside	111-125	annexin A2	Homo sapiens	36-45
9237635-9	1997	It is suggested that the soluble octylglucoside fraction may represent a special lipidic membrane compartment where the NSF attachment proteins and the cytosolic proteins like annexin 2 and rab3a may become concentrated upon stimulation of the cell.	octyl-beta-D-glucoside	33-47	annexin A2	Homo sapiens	176-185
9237635-9	1997	It is suggested that the soluble octylglucoside fraction may represent a special lipidic membrane compartment where the NSF attachment proteins and the cytosolic proteins like annexin 2 and rab3a may become concentrated upon stimulation of the cell.	octyl-beta-D-glucoside	33-47	RAB3A, member RAS oncogene family	Homo sapiens	190-195
9218131-5	1997	The EGTA-resistant membrane-bound annexin II could be partially extracted by 1% Triton X-100 or 60 mM n-octyl-beta-D-glucopyranoside, and completely by 30 mM CHAPS or 0.1% deoxycholate.	octyl-beta-D-glucoside	102-132	annexin A2	Homo sapiens	34-44
9315619-4	1997	Unlike those on epithelial cells, the GPI-anchored proteins of lymphocytes (Thy-1 and the heat stable antigen CD24) were enriched in the floating fractions after extraction over a wide range of octylglucoside concentrations.	octyl-beta-D-glucoside	194-208	Thy-1 cell surface antigen	Homo sapiens	76-81
9315619-5	1997	In contrast, the floatability of endothelial GPI-anchored CD59 was markedly diminished, not only by octylglucoside, but also by increasing concentrations of Triton X-100.	octyl-beta-D-glucoside	100-114	CD59 molecule (CD59 blood group)	Homo sapiens	58-62
9315619-7	1997	Analysis of the intracellular acylated molecules revealed that a significant amount of p56(lck) was always associated with the floating GPI-rich fractions of lymphocytes when extracted by Triton X-100 or octylglucoside at 4 degrees C, while the behaviour of endothelial cell caveolin was comparable to that of CD59.	octyl-beta-D-glucoside	204-218	interferon induced protein with tetratricopeptide repeats 1	Homo sapiens	87-90
9042955-8	1997	The DAP was found to be contained in the sarcoglycan fraction which was prepared by treatment of the dystrophin-DAP complex with n-octyl beta-D-glucoside and crosslinked with beta- and/or gamma-sarcoglycan by a chemical crosslinker, dithiobis(succinimidyl propionate).	octyl-beta-D-glucoside	129-153	dystrophin	Homo sapiens	101-111
9042955-8	1997	The DAP was found to be contained in the sarcoglycan fraction which was prepared by treatment of the dystrophin-DAP complex with n-octyl beta-D-glucoside and crosslinked with beta- and/or gamma-sarcoglycan by a chemical crosslinker, dithiobis(succinimidyl propionate).	octyl-beta-D-glucoside	129-153	death associated protein	Homo sapiens	112-115
8943782-5	1996	The highly active 17 beta-HSD1 preparation was successfully crystallized in the presence of NADP-, polyethylene glycol, beta-octylglucoside and glycerol, resulting in the first diffraction quality crystals of any steroid-converting enzyme from a human source.	octyl-beta-D-glucoside	120-139	hydroxysteroid 17-beta dehydrogenase 1	Homo sapiens	18-30
8954151-11	1996	Transmission electron microscopy of purified MAO B was performed using protein prepared by octyl glucoside extraction.	octyl-beta-D-glucoside	91-106	monoamine oxidase B	Bos taurus	45-50
9048951-1	1997	The major intrinsic protein (MIP) from bovine lens fibre membranes has been purified from unstripped membranes using a single ion-exchange chromatography step (MonoS) in the non-ionic detergent octyl-beta-D-glucopyranoside (OG).	octyl-beta-D-glucoside	194-222	major intrinsic protein of lens fiber	Bos taurus	4-27
9048951-1	1997	The major intrinsic protein (MIP) from bovine lens fibre membranes has been purified from unstripped membranes using a single ion-exchange chromatography step (MonoS) in the non-ionic detergent octyl-beta-D-glucopyranoside (OG).	octyl-beta-D-glucoside	194-222	major intrinsic protein of lens fiber	Bos taurus	29-32
9048951-1	1997	The major intrinsic protein (MIP) from bovine lens fibre membranes has been purified from unstripped membranes using a single ion-exchange chromatography step (MonoS) in the non-ionic detergent octyl-beta-D-glucopyranoside (OG).	octyl-beta-D-glucoside	224-226	major intrinsic protein of lens fiber	Bos taurus	4-27
9048951-1	1997	The major intrinsic protein (MIP) from bovine lens fibre membranes has been purified from unstripped membranes using a single ion-exchange chromatography step (MonoS) in the non-ionic detergent octyl-beta-D-glucopyranoside (OG).	octyl-beta-D-glucoside	224-226	major intrinsic protein of lens fiber	Bos taurus	29-32
8529642-3	1995	The immunochemical properties of the reconstituted oxidase made use of monoclonal antibodies raised against membrane-bound and octyl-glucoside-extracted cytochrome b.	octyl-beta-D-glucoside	127-142	mitochondrially encoded cytochrome b	Homo sapiens	153-165
8776886-3	1996	Two-dimensional crystals of C-terminally truncated rhodopsin reconstituted from octyl glucoside solution formed in a p222(1) lattice (a = 44 A, b = 131 A).	octyl-beta-D-glucoside	80-95	rhodopsin	Bos taurus	51-60
8530366-8	1995	The formation of UPII homodimers is sensitive, however, to octyl glucoside that can solubilize the AUMs.	octyl-beta-D-glucoside	59-74	uroplakin 2	Homo sapiens	17-21
8679658-1	1996	The self-association state of the human red cell glucose transporter (Glut1) in octaethylene glycol n-dodecyl ether (C12E8) and n-octyl beta-D-glucopyranoside (OG) solution was analyzed in the presence of reductant by gel filtration with light-scattering, refractivity and absorbance detection, and by ultracentrifugation.	octyl-beta-D-glucoside	128-158	solute carrier family 2 member 1	Homo sapiens	70-75
8679658-1	1996	The self-association state of the human red cell glucose transporter (Glut1) in octaethylene glycol n-dodecyl ether (C12E8) and n-octyl beta-D-glucopyranoside (OG) solution was analyzed in the presence of reductant by gel filtration with light-scattering, refractivity and absorbance detection, and by ultracentrifugation.	octyl-beta-D-glucoside	160-162	solute carrier family 2 member 1	Homo sapiens	70-75
7487928-11	1995	Further purification of OG extracts using concanavalin A and wheat-germ lectin columns resulted in the separation of transport activity from the bulk (but not all) of alpha 3 beta 1 integrin without loss of the transport activity.	octyl-beta-D-glucoside	24-26	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	175-181
7626019-6	1995	However, rat, dog and normal human SP-A isolated by a novel method, involving extraction from pulmonary surfactant by using n-octyl beta-D-glucopyranoside and subsequent purification by cation-exchange chromatography, were able to elicit an oxidative burst in rat as well as normal human alveolar macrophages.	octyl-beta-D-glucoside	124-154	surfactant protein A1	Homo sapiens	35-39
8576649-8	1995	The delipidated apolipoprotein fragments of oxLDL that had been solubilized in beta-octylglucoside stimulated the production of IL-1 alpha by the foam cells to a greater degree than the lipid extract, while reductively methylated oxLDL did not.	octyl-beta-D-glucoside	79-98	interleukin-1 alpha	Oryctolagus cuniculus	128-138
7536473-4	1995	In this study we show that neutrophil AlkPase, FcRIII, and DAF display differential extractibility; they are relatively insensitive to TX-100 solubilization at 4 degrees C, but are readily extracted with TX-100 at 37 degrees C or by the detergent octyl glucoside at 4 degrees C. The differential extractibility of these GPI-anchored proteins is the same in unstimulated cells, where these proteins exist primarily in an intracellular pool, and stimulated cells, where they are expressed principally at the cell surface.	octyl-beta-D-glucoside	247-262	Fc gamma receptor IIIa	Homo sapiens	47-53
7612242-4	1995	The presence of p12 in the cytoplasmic fraction of infected cells has allowed the purification of the protein by a simple two-step procedure of aqueous phase partition and octyl-glucoside solubilization.	octyl-beta-D-glucoside	172-187	DNA polymerase epsilon 4, accessory subunit	Homo sapiens	16-19
7756303-3	1995	Twenty-three synthetic FPR-mimetic and control peptides were tested for their ability to disrupt functionally active complexes of FPR and Gi2 in octyl glucoside, assayed by changes in sedimentation rates of FPR in detergent-containing sucrose gradients.	octyl-beta-D-glucoside	145-160	formyl peptide receptor 1	Homo sapiens	130-133
7756303-3	1995	Twenty-three synthetic FPR-mimetic and control peptides were tested for their ability to disrupt functionally active complexes of FPR and Gi2 in octyl glucoside, assayed by changes in sedimentation rates of FPR in detergent-containing sucrose gradients.	octyl-beta-D-glucoside	145-160	formyl peptide receptor 1	Homo sapiens	130-133
7532004-6	1995	Glycosylated and nonglycosylated CHIP28 remained tightly associated when solubilized in octyl beta-D-glucoside (OG) and could not be separated by conventional chromatographic procedures.	octyl-beta-D-glucoside	88-110	aquaporin 1 (Colton blood group)	Homo sapiens	33-39
7532004-6	1995	Glycosylated and nonglycosylated CHIP28 remained tightly associated when solubilized in octyl beta-D-glucoside (OG) and could not be separated by conventional chromatographic procedures.	octyl-beta-D-glucoside	112-114	aquaporin 1 (Colton blood group)	Homo sapiens	33-39
7723792-3	1995	The TLF apolipoproteins were purified by anion exchange chromatography in the presence of the nonionic detergent octylglucoside and a reconstitution method was developed which allowed the role of the individual apolipoproteins and different lipids to be assessed.	octyl-beta-D-glucoside	113-127	TATA-box binding protein like 1	Homo sapiens	4-7
7848273-9	1995	MIP26 was extracted with n-octyl beta-D-glucopyranoside and then purified on an affinity gel column.	octyl-beta-D-glucoside	25-55	major intrinsic protein of lens fiber	Rattus norvegicus	0-5
7738118-10	1995	PM InsP3R-L of Pam cells was hardly extracted by treatment with 0.5% Triton X-100 or 60 mM octyl-glucoside in a cytoskeleton-stabilizing buffer for 15 minutes at 4 degrees C. The results show that the distribution of caveolae bearing PM InsP3R-L changes when the actin cytoskeleton is modified.	octyl-beta-D-glucoside	91-106	inositol 1,4,5-trisphosphate receptor 1	Mus musculus	3-9
18966211-5	1995	In contrast, the use of the zwitterionic surfactant and octyl-beta-d-glucoside as an affinity ligand proved to be effective for the extraction of hexokinase.	octyl-beta-D-glucoside	56-78	hexokinase 1	Homo sapiens	146-156
7947984-0	1994	Characterization of complex formation between Gi2 and octyl glucoside solubilized neutrophil N-formyl peptide chemoattractant receptor by sedimentation velocity.	octyl-beta-D-glucoside	54-69	formyl peptide receptor 1	Homo sapiens	93-134
7734245-1	1994	Cytochrome P450scc can be reconstituted successfully into large unilamellar phospholipid vesicles by a combined octylglucoside dialysis/adsorption method.	octyl-beta-D-glucoside	112-126	cholesterol side-chain cleavage enzyme, mitochondrial	Bos taurus	0-18
7979387-9	1994	The apparent molecular mass of hCox-2, determined by gel filtration chromatography in the presence of 2.0% beta-octylglucoside, is consistent with a dimeric structure.	octyl-beta-D-glucoside	107-126	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	31-37
7699013-4	1994	Analysis of the distribution of the alpha 6 and beta 1 integrin subunits in the gradients showed that they migrate as a large complex after extraction of cells with octylglucoside, but not after Triton X-100 extraction.	octyl-beta-D-glucoside	165-179	integrin subunit beta 1	Homo sapiens	48-63
7920712-7	1994	STP1-His6 protein is functionally active after solubilization with octyl-beta-D-glucoside, which was shown by insertion of the protein into proteoliposomes by detergent dilution and determination of the resulting transport capacity.	octyl-beta-D-glucoside	67-89	Stp1p	Saccharomyces cerevisiae S288C	0-4
8026484-0	1994	Dissociation of the complex of dystrophin and its associated proteins into several unique groups by n-octyl beta-D-glucoside.	octyl-beta-D-glucoside	100-124	dystrophin	Homo sapiens	31-41
8026484-3	1994	In the present study, we found that the purified dystrophin-DAP complex was dissociated into several groups by n-octyl-beta-D-glucoside treatment.	octyl-beta-D-glucoside	111-135	dystrophin	Homo sapiens	49-59
7920712-7	1994	STP1-His6 protein is functionally active after solubilization with octyl-beta-D-glucoside, which was shown by insertion of the protein into proteoliposomes by detergent dilution and determination of the resulting transport capacity.	octyl-beta-D-glucoside	67-89	1-(5-phosphoribosyl)-5- ((5-phosphoribosylamino)methylideneamino)imidazole-4-carboxamide isomerase HIS6	Saccharomyces cerevisiae S288C	5-9
8054657-2	1994	The bee PHM has a molecular weight of 71,000, is membrane associated but can be solubilized with a detergent (n-octyl-beta-D-glucopyranoside), and cross-reacts with rabbit antibodies generated toward bacterially expressed rat PHM.	octyl-beta-D-glucoside	110-140	peptidylglycine alpha-hydroxylating monooxygenase	Apis mellifera	8-11
8130257-3	1994	SP-A was isolated from bovine or rat lung surfactant by extraction with 1-butanol and octyl beta-D-glucopyranoside.	octyl-beta-D-glucoside	86-114	pulmonary surfactant-associated protein A	Bos taurus	0-4
11537708-4	1993	The nonionic detergent known as n-octyl glucoside (n-octyl beta-D-glucopyranoside) was found to give the best combination of selectivity, yield, and maintenance of enzymatic activity of the human EGFR.	octyl-beta-D-glucoside	32-49	epidermal growth factor receptor	Homo sapiens	196-200
8375510-2	1993	EGF receptor dephosphorylation was clearly faster than PDGF receptor dephosphorylation and strongly inhibited by Triton X-100 and octylglucoside, whereas PDGF receptor dephosphorylation was to a lesser extent detergent-susceptible.	octyl-beta-D-glucoside	130-144	epidermal growth factor	Mus musculus	0-3
8348566-2	1993	Proteins and lipids of crude membranes of SL2 murine lymphosarcoma cells were partially solubilized with octylglucoside.	octyl-beta-D-glucoside	105-119	matrix metallopeptidase 10	Mus musculus	42-45
8335107-1	1993	Using octyl glucoside-solubilized cell extracts from human fibroblasts during growth phase to G0/G1 arrest state, we found that while the number of M(r) 120 kDa rasGTPase-activating protein (p120GAP) molecules per cell decreases to half its original levels, the amount of neurofibromatosis type 1 gene product (NF1, a neurofibromin) remains constant during the transition.	octyl-beta-D-glucoside	6-21	RAS p21 protein activator 1	Homo sapiens	191-198
8505299-8	1993	Incubation of the particulate fraction obtained from BK-stimulated and nonstimulated cells with 10 mM n-octyl-beta-D-glucopyranoside resulted in a differential solubilization of the HR-PLA2 activity.	octyl-beta-D-glucoside	102-132	kininogen 1	Bos taurus	53-55
8505299-8	1993	Incubation of the particulate fraction obtained from BK-stimulated and nonstimulated cells with 10 mM n-octyl-beta-D-glucopyranoside resulted in a differential solubilization of the HR-PLA2 activity.	octyl-beta-D-glucoside	102-132	LOC104974671	Bos taurus	185-189
8505299-10	1993	HR-PLA2 activity in the octyl glucoside extract of the particulate fraction from stimulated cells co-sedimented in sucrose gradients with the cytosolic PLA2.	octyl-beta-D-glucoside	24-39	LOC104974671	Bos taurus	3-7
8505299-10	1993	HR-PLA2 activity in the octyl glucoside extract of the particulate fraction from stimulated cells co-sedimented in sucrose gradients with the cytosolic PLA2.	octyl-beta-D-glucoside	24-39	LOC104974671	Bos taurus	152-156
11537708-4	1993	The nonionic detergent known as n-octyl glucoside (n-octyl beta-D-glucopyranoside) was found to give the best combination of selectivity, yield, and maintenance of enzymatic activity of the human EGFR.	octyl-beta-D-glucoside	51-81	epidermal growth factor receptor	Homo sapiens	196-200
8429563-1	1993	The human pancreatic lipase-porcine procolipase complex has been crystallized in space group P3(2)21 (a = b = 80.3 A and c = 251 A) from a solution containing polyethylene glycol, NaCl and beta-octyl glucoside.	octyl-beta-D-glucoside	189-209	pancreatic lipase	Homo sapiens	10-27
8095161-6	1993	Octyl glucoside in the low mM range also supported the ATPase, while deoxycholate destroyed all activity at 1 mM.	octyl-beta-D-glucoside	0-15	dynein axonemal heavy chain 8	Homo sapiens	55-61
1402914-1	1992	5-Hydroxytryptamine3 (5-HT3) receptor-type binding sites were solubilised from NG108-15 mouse neuroblastoma x rat glioma hybrid cells using five different detergents [n-octyl-beta-D-glucoside, Triton X-100, 3-[3-(cholamidopropyl)dimethylammonio]-1-propanesulphonate (CHAPS), sodium cholate, and deoxycholate] and the solubilisation efficiencies compared.	octyl-beta-D-glucoside	167-191	5-hydroxytryptamine (serotonin) receptor 3A	Mus musculus	0-28
1355580-5	1992	In conclusion, our results show that Arg abolishes the inhibitory effect of OG administration on the GHRH-induced GH response in man.	octyl-beta-D-glucoside	76-78	growth hormone releasing hormone	Homo sapiens	101-105
1355580-5	1992	In conclusion, our results show that Arg abolishes the inhibitory effect of OG administration on the GHRH-induced GH response in man.	octyl-beta-D-glucoside	76-78	growth hormone 1	Homo sapiens	101-103
1597144-1	1992	When n-octyl-beta-D-glucoside was used in several detergents to extract active avian pancreatic polypeptide (APP) receptors, a specific binding of [125I]APP to the solubilized chicken cerebellar and porcine hippocampal membranes was found.	octyl-beta-D-glucoside	5-29	pancreatic hormone	Gallus gallus	85-123
1312805-5	1992	On the partially purified insulin receptor, Na deoxycholate inhibited both insulin receptor activities; octyl-beta-D-glucopyranoside and octyl-beta-D-thioglucopyranoside decreased insulin binding and kinase activation as their concentration increased, particularly above their respective critical micellar concentration (CMC).	octyl-beta-D-glucoside	104-132	insulin	Homo sapiens	26-33
1500090-4	1992	Studies presented here demonstrate that if another well known detergent, octyl-beta-D-glucopyranoside (octyl glucoside), is utilized in place of digitonin, mIg receptors are immunoprecipitated from B cell lysates in association with several newly identified proteins, whose phosphorylation is also G protein dependent.	octyl-beta-D-glucoside	73-101	chemokine (C-X-C motif) ligand 9	Mus musculus	156-159
1500090-4	1992	Studies presented here demonstrate that if another well known detergent, octyl-beta-D-glucopyranoside (octyl glucoside), is utilized in place of digitonin, mIg receptors are immunoprecipitated from B cell lysates in association with several newly identified proteins, whose phosphorylation is also G protein dependent.	octyl-beta-D-glucoside	103-118	chemokine (C-X-C motif) ligand 9	Mus musculus	156-159
1560018-2	1992	Optimum enzyme activity for the deacylation of PLP was obtained in 0.5% Triton X-100, 1 mM dithiothreitol at pH 7.0 and at 37 degrees C. Other detergents (octyl beta-D-glucoside, Nonidet P-40, and Tween 20) have little or no effect, whereas deacylation was completely abolished by 0.1% sodium dodecyl sulfate or boiling the membrane fraction for 5 min prior to incubation.	octyl-beta-D-glucoside	155-177	proteolipid protein 1	Rattus norvegicus	47-50
1312805-13	1992	These alterations in the oligomerization status of the insulin receptor may explain the deleterious effects observed with both Chaps and octylglucoside at higher concentrations.	octyl-beta-D-glucoside	137-151	insulin receptor	Homo sapiens	55-71
1312930-0	1992	Effect of KCl on the interactions between NADPH:cytochrome P-450 reductase and either cytochrome c, cytochrome b5 or cytochrome P-450 in octyl glucoside micelles.	octyl-beta-D-glucoside	137-152	cytochrome p450 oxidoreductase	Homo sapiens	42-74
1312930-0	1992	Effect of KCl on the interactions between NADPH:cytochrome P-450 reductase and either cytochrome c, cytochrome b5 or cytochrome P-450 in octyl glucoside micelles.	octyl-beta-D-glucoside	137-152	cytochrome c, somatic	Homo sapiens	86-98
1312930-0	1992	Effect of KCl on the interactions between NADPH:cytochrome P-450 reductase and either cytochrome c, cytochrome b5 or cytochrome P-450 in octyl glucoside micelles.	octyl-beta-D-glucoside	137-152	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	48-64
1878372-1	1991	The human red cell glucose transporter (Glut 1) was purified by ion-exchange chromatography in the presence of octyl glucoside.	octyl-beta-D-glucoside	111-126	solute carrier family 2 member 1	Homo sapiens	40-46
1483409-4	1992	However, in octyl glucoside, at and above the critical micelle concentration, the peptide adopts a beta-sheet conformation.	octyl-beta-D-glucoside	12-27	amyloid beta precursor protein	Homo sapiens	97-103
1659898-10	1991	Octyl glucoside, a nonionic detergent, mimicked some of the effects of CaM antagonists, suggesting that the antagonists act by interfering with protein-protein interactions.	octyl-beta-D-glucoside	0-15	calmodulin	Bos taurus	71-74
1911761-3	1991	The 88-kDa polypeptide of MTP (88K) was dissociated from PDI by using chaotropic agents (NaClO4 and KSCN), low concentrations of a denaturant (guanidine hydrochloride) or a nondenaturing detergent (octyl glucoside).	octyl-beta-D-glucoside	198-213	microsomal triglyceride transfer protein	Homo sapiens	26-29
1878372-9	1991	Freshly prepared Glut 1 retained high activity after separation from membrane lipids on a TSKgel G3000SW column in the presence of 40 mM octyl glucoside and 1 mM PS or PC.	octyl-beta-D-glucoside	137-152	solute carrier family 2 member 1	Homo sapiens	17-23
1878372-11	1991	The presence of a phospholipid was thus essential for retention of high activity of the Glut 1 in octyl glucoside and PC was nearly as effective as PS.	octyl-beta-D-glucoside	98-113	solute carrier family 2 member 1	Homo sapiens	88-94
1902223-5	1991	Solubilization of p28 required buffers containing 1% octylglucoside and at least 300 mM KCl.	octyl-beta-D-glucoside	53-67	golgi SNAP receptor complex member 1	Rattus norvegicus	18-21
1849900-4	1991	We next studied the effect of 1 x 10(-5) M Ca2+ on the kinetic properties of DGK employing a beta-octyl glucoside mixed micellar assay system.	octyl-beta-D-glucoside	93-113	diacylglycerol kinase beta	Homo sapiens	77-80
1826933-8	1991	The detergent octylglucoside facilitated the delipidated (H+)ATPase reinsertion probably by promoting both a proper protein conformation and hydrophobic defects in the bilayer.	octyl-beta-D-glucoside	14-28	ATPase	Zea mays	58-67
2995429-3	1985	TPO was prepared from Graves" thyroid glands, solubilized by n-octyl glucoside, and its activity was assayed by the guaiacol method.	octyl-beta-D-glucoside	61-78	thyroid peroxidase	Homo sapiens	0-3
2373740-5	1990	In accordance with this, C-CAM was effectively incorporated into phosphatidylcholine liposomes by dialysis from octylglucoside-containing solutions.	octyl-beta-D-glucoside	112-126	CEA cell adhesion molecule 1	Rattus norvegicus	25-30
2166590-7	1990	Octyl glucoside and sodium cholate also uncoupled receptor regulation of phospholipase C but only at concentrations where solubilization of membrane proteins occurred.	octyl-beta-D-glucoside	0-15	LOC100009319	Oryctolagus cuniculus	73-88
2341401-2	1990	The major protein from the bovine lens fiber cell membranes, the 26-kilodalton protein (major intrinsic protein (MIP26)), has been solubilized in n-octyl-beta-D-glucopyranoside and purified by gel filtration.	octyl-beta-D-glucoside	146-176	major intrinsic protein of lens fiber	Bos taurus	113-118
2294117-3	1990	Diffraction quality crystals of the synthetic apolipoprotein E fragment129-169 have been obtained at room temperature by vapor diffusion with polyethylene glycol in the presence of the nonionic detergent beta-octylglucoside.	octyl-beta-D-glucoside	204-223	apolipoprotein E	Homo sapiens	46-62
34382261-5	2021	OG treatment alleviated the OVX-CUMS induced dysfunction of hypothalamic-pituitary-ovarian (HPO) axis by increased serum estradiol (E2) and decreased ovarian hormones follicle stimulating hormone (FSH), luteinizing hormone (LH), and gonadotropin-releasing hormone (GnRH) in serum.	octyl-beta-D-glucoside	0-2	gonadotropin releasing hormone 1	Mus musculus	233-263
34382261-5	2021	OG treatment alleviated the OVX-CUMS induced dysfunction of hypothalamic-pituitary-ovarian (HPO) axis by increased serum estradiol (E2) and decreased ovarian hormones follicle stimulating hormone (FSH), luteinizing hormone (LH), and gonadotropin-releasing hormone (GnRH) in serum.	octyl-beta-D-glucoside	0-2	gonadotropin releasing hormone 1	Mus musculus	265-269
35585885-9	2022	Meanwhile, the inhibitory effect of OG on autophagy was reversed by the Nrf2 inhibitor ML385.Conclusively, OG attenuated bone loss by inhibiting formation, differentiation, and bone resorption activities of osteoclast.	octyl-beta-D-glucoside	107-109	nuclear factor, erythroid derived 2, like 2	Mus musculus	72-76
34118644-1	2021	This study aimed to discuss the expression of angiogenesis-related proteins in bone marrow mesenchymal stem cells (BMSCs) induced by osteoprotegerin (OGP) during osteogenic differentiation in rats, and to analyze the effect of fracture healing inflammatory factor TNF-alpha on the osteogenic differentiation of BMSCs of rats.	octyl-beta-D-glucoside	150-153	TNF receptor superfamily member 11B	Rattus norvegicus	133-148
35585885-8	2022	Of note, the effect of OG on Nrf2/Keap1 signaling was neutralized by the mTOR inhibitor rapamycin.	octyl-beta-D-glucoside	23-25	nuclear factor, erythroid derived 2, like 2	Mus musculus	29-33
35585885-8	2022	Of note, the effect of OG on Nrf2/Keap1 signaling was neutralized by the mTOR inhibitor rapamycin.	octyl-beta-D-glucoside	23-25	kelch-like ECH-associated protein 1	Mus musculus	34-39
35585885-8	2022	Of note, the effect of OG on Nrf2/Keap1 signaling was neutralized by the mTOR inhibitor rapamycin.	octyl-beta-D-glucoside	23-25	mechanistic target of rapamycin kinase	Mus musculus	73-77
35435300-10	2022	Differentiation marker studies using human keratinocytes showed that gene expression of involucrin and serine palmitoyltransferase was upregulated by OG, which was almost equivalent concentration to OG formulation 80 ppm, suggesting that OGs can enhance turnover of the skin epidermis.	octyl-beta-D-glucoside	150-152	involucrin	Homo sapiens	88-98
35435300-10	2022	Differentiation marker studies using human keratinocytes showed that gene expression of involucrin and serine palmitoyltransferase was upregulated by OG, which was almost equivalent concentration to OG formulation 80 ppm, suggesting that OGs can enhance turnover of the skin epidermis.	octyl-beta-D-glucoside	199-201	involucrin	Homo sapiens	88-98