PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 16311081-2 2006 An immunosorbent of polyclonal anti-bovine serum albumin (BSA) antibodies immobilized on CNBR agarose is used in the on-line mode for selective sample pretreatment. Sepharose 94-101 albumin Homo sapiens 43-56 17210183-2 2007 Blue-Sepharose is often used to remove bovine serum albumin (BSA) from samples, but when we applied BSA to Blue-Sepharose in 20 mM phosphate, pH 7.0, 50%-60% of the protein flowed through the column; however, complete binding of BSA was achieved by the addition of 2 M ammonium sulfate (AS) to the column equilibration buffer and the sample. Sepharose 5-14 albumin Homo sapiens 46-59 10076829-8 1998 The characteristics of electrophoretic binding of HSA on Blue Sepharose Fast Flow are examined. Sepharose 62-71 albumin Homo sapiens 50-53 14735978-3 2003 An experimental study on the interplay of sorbent structure and fluid phase conditions (pH) has been carried out examining adsorption and transport of bovine serum albumin (BSA) and a monoclonal antibody (IgG 2a) on SP Sepharose Fast Flow and SP Sepharose XL. Sepharose 219-228 albumin Homo sapiens 158-171 9420169-0 1997 Detection and semiquantitation of albumin forms in fresh human plasma separated on gradient polyacrylamide gel by means of electroblotting on agarose gel matrix. Sepharose 142-149 albumin Homo sapiens 34-41 9420169-6 1997 After staining of the agarose gel, it revealed the presence of seven stained bands of albumin in addition to the monomer. Sepharose 22-29 albumin Homo sapiens 86-93 9188815-3 1997 Albumin was separated by chromatography on Blue-Sepharose. Sepharose 48-57 albumin Homo sapiens 0-7 7580117-6 1995 HSA or BSA linked to Sepharose was incubated with a 15, 20, or 24 mer S-ODN followed by the addition of selected drugs known to be highly protein bound (nifedipine, warfarin, midazolam, probenecid, indomethacin, and mitoxantrone). Sepharose 21-30 albumin Homo sapiens 7-10 8639481-4 1996 Alb-hep surfaces incubated in plasma which was preexposed to heparin-Sepharose retained 30% of their initial activity. Sepharose 69-78 albumin Homo sapiens 0-3 34954298-4 2022 Agarose native gel electrophoresis showed that aggregation of bovine serum albumin (BSA) induced by heating was slightly reduced by NaCl and ArgHCl. Sepharose 0-7 albumin Homo sapiens 69-82 1642965-1 1992 The effect of phenprocoumon enantiomers on the stereoselective binding of 3-substituted 1,4-benzodiazepines to human serum albumin (HSA) was studied by chromatography on HSA-Sepharose column. Sepharose 174-183 albumin Homo sapiens 117-130 8075524-1 1994 A method for the preparation of a p-aminobenzene sulphonyl ethyl containing crosslinked Sepharose 4B (ABSE-Sepharose 4B-CL) is described, trypsin, bovine serum albumin (BSA) and concanavalin A (Con A) were immobilized onto this matrix by diazotization. Sepharose 88-100 albumin Homo sapiens 154-167 1632506-2 1992 In this assay an agarose replica of the polyacrylamide gel which contains hyaluronic acid and bovine serum albumin (BSA) was used. Sepharose 17-24 albumin Homo sapiens 101-114 2268430-3 1990 Fractions from Q Sepharose chromatography, eluted with a linear gradient 0-1.0 M NaCl and subsequently acetylated, proved to be the most effective method for obtaining deoxyribonuclease-free bovine serum albumin. Sepharose 17-26 albumin Homo sapiens 198-211 2275755-0 1990 Thyroxine binding to human serum albumin immobilized on sepharose and effects of nonprotein albumin-binding plasma constituents. Sepharose 56-65 albumin Homo sapiens 27-40 6955933-2 1982 It was found that the main component was anionic and was eluted between albumin and lysozyme on Sepharose. Sepharose 96-105 albumin Homo sapiens 72-79 3511088-4 1986 Hybridoma supernatants exhibiting dual reactivity were absorbed over HIgG and bovine serum albumin (BSA)-Sepharose immunoabsorbent columns. Sepharose 105-114 albumin Homo sapiens 85-98 34723292-3 2021 In this paper, we carried out an innovative study on the ability of bovine serum albumin stabilized gold nanoclusters (BSA-AuNCs) to perform as reliable label-free contrast agents for the visualization of tissue-like agarose phantoms via TPE-FLIM. Sepharose 217-224 albumin Homo sapiens 75-88 35133130-3 2022 As evidenced by agarose gel electrophoresis and liquid chromatography-mass spectrometry, it could realize the fluorescent labeling of human serum albumin (HSA) through a thiol-cyanimide addition. Sepharose 16-23 albumin Homo sapiens 140-153 3475025-0 1987 Interferometric determination of the effective diffusion coefficient of albumin in single sepharose beads. Sepharose 90-99 albumin Homo sapiens 72-79 24253644-2 1984 Cyanogen-bromide-activated agarose beads were coated with protein (gelatine or bovine serum albumin) and lectins were subsequently linked to the protein layer using glutaraldehyde. Sepharose 27-34 albumin Homo sapiens 86-99 6839503-0 1983 Determination of a glycosyl subunit of human serum albumin by concanavalin A-sepharose. Sepharose 77-86 albumin Homo sapiens 51-58 6839503-3 1983 The glycosyl albumin bound to concanavalin-A Sepharose was homogeneous when examined by immunoelectrophoresis and sodium dodecyl-sulphate polyacrylamide electrophoresis, whereas it showed a microheterogeneity when tested by isoelectric focusing. Sepharose 45-54 albumin Homo sapiens 13-20 351754-0 1978 Differences in the isoelectric focussing pattern of antibodies to human serum albumin eluted from an immunoadsorbent (HSA-sepharose) with thiocyanate ions. Sepharose 122-131 albumin Homo sapiens 78-85 7261401-4 1981 Albumin was transported by electrophoresis into the agarose gels, in which zones of immunoprecipitates were formed. Sepharose 52-59 albumin Homo sapiens 0-7 657550-1 1978 The affinity adsorbent Cibacron Blue F3GA-Sepharose 4-B has been used to develop a binding assay for human serum albumin. Sepharose 42-55 albumin Homo sapiens 107-120 333666-2 1977 Separation of free and bound steroid was effected by Sepharose-coupled antiprogesterone-11alpha-hemisuccinyl bovine serum albumin antiserum (Sepharose-antisera). Sepharose 53-62 albumin Homo sapiens 116-129 33586042-8 2021 ALB-Cys34SNO was prepared by reacting n-butylnitrite with albumin after selective extraction from plasma of a healthy donor on HiTrapBlue Sepharose cartridges. Sepharose 138-147 albumin Homo sapiens 0-3 1249429-1 1976 Human serum albumin-Sepharose was prepared by coupling human serum albumin to cyanogen bromide activated Sepharose 4B. Sepharose 20-29 albumin Homo sapiens 6-19 1249429-1 1976 Human serum albumin-Sepharose was prepared by coupling human serum albumin to cyanogen bromide activated Sepharose 4B. Sepharose 20-29 albumin Homo sapiens 61-74 1249429-1 1976 Human serum albumin-Sepharose was prepared by coupling human serum albumin to cyanogen bromide activated Sepharose 4B. Sepharose 105-114 albumin Homo sapiens 6-19 1217705-0 1975 Albumin immobilized on agarose as a tool for measuring ligand binding of proteins or peptides. Sepharose 23-30 albumin Homo sapiens 0-7 33586042-9 2021 ALB-Cys34SNO was used in platelet aggregation measurements after extended purification on HiTrapBlue Sepharose and enrichment by ultrafiltration (cutoff, 20 kDa). Sepharose 101-110 albumin Homo sapiens 0-3 19671121-7 2009 Albumin was measured by using semiquantitative test strips, by agarose gel electrophoresis, and by an automated immunoturbidimetric assay designed for human samples (considered as the gold standard). Sepharose 63-70 albumin Homo sapiens 0-7 33196158-5 2020 Hydrophobic oil microparticles are produced by the simple plasma treatment of the DM, and agarose microparticles encapsulating bovine serum albumin (in a well-dispersed state) are produced by submerging the DM in fluorinated oil. Sepharose 90-97 albumin Homo sapiens 134-147 31537306-1 2020 Our previous studies on protein adsorption to the anion-exchangers of poly(ethylenimine) (PEI)-grafted Sepharose FF found that both adsorption capacity and uptake rate of bovine serum albumin (BSA) increased greatly when the PEI grafting density reached over a critical ionic capacity (cIC) due to the 3D protein binding and occurrence of "chain delivery" of bound proteins. Sepharose 103-112 albumin Homo sapiens 178-191 26164303-3 2015 The HD-ALB adduct was isolated from HD-exposed plasma with blue Sepharose. Sepharose 64-73 albumin Homo sapiens 7-10 33454336-8 2021 We have extracted bands of bovine serum albumin from the agarose native gel for sodium dodecylsulfate gel electrophoresis analysis, showing degradation of aged sample. Sepharose 57-64 albumin Homo sapiens 34-47 32043104-11 2020 The combination of ITC, agarose gel electrophoresis (AGE) and zeta potential showed that one HSA could bind 8 +- 1 DHLA-AuNCs and one Trf could bind 7 +- 2 DHLA-AuNCs, which was quite different from the conventional model of protein coronas. Sepharose 24-31 albumin Homo sapiens 93-96 28114763-5 2017 These ideas are validated in agarose gels loaded with latex particles stabilized by adsorbed bovine serum albumin. Sepharose 29-36 albumin Homo sapiens 100-113 26413976-0 2015 Facile synthesis of nano-sized agarose based amino acid-Its pH-dependent protein-like behavior and interactions with bovine serum albumin. Sepharose 31-38 albumin Homo sapiens 124-137 25465013-1 2014 We have previously studied poly(ethylenimine) (PEI)-grafted Sepharose FF resins for ion-exchange chromatography of bovine serum albumin (BSA), and found the presence of a critical ionic capacity (cIC, 600mmol/L for BSA), above which both BSA adsorption capacity and uptake rates increased drastically. Sepharose 60-69 albumin Homo sapiens 122-135 22740250-0 2012 Tris(hydroxymethyl)aminomethane-functionalized agarose particles: parameters affecting the binding of bovine serum albumin. Sepharose 47-54 albumin Homo sapiens 109-122 18947830-3 2008 The adsorption equilibrium and kinetics of lysozyme and bovine serum albumin (BSA) to AI-Sepharose were determined by batch adsorption experiments at different conditions to provide insight into the adsorption properties of the medium. Sepharose 89-98 albumin Homo sapiens 63-76