PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 25860295-6 2015 Bovine fibrinogen immobilized on CNBr-activated Sepharose 4B beads showed affinity for hemin, Sn-PPIX, Zn-PPIX, and iron-free PPIX in the order Sn-PPIX < iron-free PPIX < hemin < Zn-PPIX. Sepharose 48-60 fibrinogen beta chain Homo sapiens 7-17 28365482-0 2017 Distributed vasculogenesis from modular agarose-hydroxyapatite-fibrinogen microbeads. Sepharose 40-47 fibrinogen beta chain Homo sapiens 63-73 28365482-16 2017 In this study, we developed small, non-aggregating agarose-hydroxyapatite-fibrinogen microbeads that contained endothelial cells and fibroblasts. Sepharose 51-58 fibrinogen beta chain Homo sapiens 74-84 11171108-4 2001 Anhydrothrombin retained affinity for various natural substrates of thrombin, including fibrinogen, factor VIII, factor XIII and protein C. In addition, these proteins were bound to anhydrothrombin-agarose in a reversible manner. Sepharose 198-205 fibrinogen beta chain Homo sapiens 88-98 23864430-2 2013 In this study, human fibrinogen was immobilized on CNBr-activated Sepharose 4B beads. Sepharose 66-78 fibrinogen beta chain Homo sapiens 21-31 23864430-3 2013 The fibrinogen beads bound hemin (iron-protoporphyrin IX: PPIX) as well as iron ion released from ferrous ammonium sulfate (FAS) more efficiently than Sepharose 4B beads alone. Sepharose 151-163 fibrinogen beta chain Homo sapiens 4-14 20002787-8 2010 Fibrinopeptides A and B (FPA and FPB, respectively) were released after fibrinogen cleavage by L-FCN-MASPs complexes captured on N-acetylcysteine-Sepharose. Sepharose 146-155 fibrinogen beta chain Homo sapiens 72-82 19595454-3 2009 Human marrow stromal cells (hMSCs) were singularly encapsulated in agarose capsules containing the immobilized matrix molecules, fibronectin and fibrinogen to ameliorate cell-matrix survival signals. Sepharose 67-74 fibrinogen beta chain Homo sapiens 145-155 15039285-6 2004 Binding of (125)I-IL-1beta to Sepharose-immobilized fibrinogen also demonstrated a single binding site with an apparent K(d) of 3.5 nM. Sepharose 30-39 fibrinogen beta chain Homo sapiens 52-62 14691567-8 2004 Sepharose beads covalently coated with either whole fibrinogen or Haptides (SB-Fib or SB-Haptide) highly adsorbed free (FITC) Haptides. Sepharose 0-9 fibrinogen beta chain Homo sapiens 52-62 14606683-1 2003 Using a combination of Cohn ethanol fractionation, virus inactivation, glycine and sodium chloride precipitation, and lysine-Sepharose affinity chromatography, a unique and rapid simplified method was developed to obtain highly purified fibrinogen for diagnostic use with both biological (Clauss method) and immunological (Jacobsson method) activity. Sepharose 125-134 fibrinogen beta chain Homo sapiens 237-247 9516457-4 1998 Binding studies were performed using bFGF immobilized on Sepharose beads and soluble 125I-labeled fibrinogen and also using Sepharose-immobilized fibrinogen and soluble 125I-bFGF. Sepharose 124-133 fibrinogen beta chain Homo sapiens 146-156 10713316-1 2000 Fibrinogen was purified by protamine-agarose chromatography from plasma from three patients after their submission to hospital due to acute myocardial infarction. Sepharose 37-44 fibrinogen beta chain Homo sapiens 0-10 9523852-4 1998 We developed a new cell haptotactic/attachment assay by using Thr and Fib covalently bound to Sepharose beads (SBs). Sepharose 94-103 fibrinogen beta chain Homo sapiens 70-73 8457652-10 1993 These clones secreted biologically active recombinant human fibrinogen, which was purified from serum-free culture media by protamine-Sepharose chromatography. Sepharose 134-143 fibrinogen beta chain Homo sapiens 60-70 7601270-3 1994 Pigeon fibrinogen, isolated from plasma by precipitation with PEG-1000 and purified over Sepharose 4B, was used to study receptor-ligand interaction. Sepharose 89-98 fibrinogen beta chain Homo sapiens 7-17 7509643-4 1994 The decrease in the fibrinogen concentration in human blood plasma caused by plasmosorption on plasminogen-Sepharose enhanced the model fibrin clot lysis by urokinase and streptokinase, however, by no more than 5-10%. Sepharose 107-116 fibrinogen beta chain Homo sapiens 20-30 8384496-2 1993 Urinary PCI bound to fibrin(ogen)-Sepharose in a heparin-dependent manner at a level about 1.6-fold higher to fibrin-Sepharose than to fibrinogen-Sepharose. Sepharose 34-43 fibrinogen beta chain Homo sapiens 135-145 8384496-3 1993 Scatchard analysis of the binding between urinary PCI and fibrin(ogen)-Sepharose showed that the Kd for fibrin-Sepharose and fibrinogen-Sepharose were 4.0 nM and 5.7 nM respectively. Sepharose 71-80 fibrinogen beta chain Homo sapiens 125-135 8128455-2 1993 First, we prepared fibrinogen-coated agarose beads (fbg-beads) as a model of platelets, and subjected them to aggregometry using TSP as an inducer. Sepharose 37-44 fibrinogen beta chain Homo sapiens 19-29 1517349-1 1992 The three proteins phosphorylase b, calmodulin and fibrinogen are adsorbed onto thioalkyl derivatives of Sepharose much more strongly than onto gels carrying the same alkyl residue coupled via a carbamate linkage. Sepharose 105-114 fibrinogen beta chain Homo sapiens 51-61 1616632-2 1992 After the cryogel was solubilized at 37 degrees C, 1:1 complex of fibrinogen and fibronectin was purified at room temperature by affinity chromatography on a gelatin-Sepharose 4B. Sepharose 166-175 fibrinogen beta chain Homo sapiens 66-76 3217916-5 1988 Degraded fibrinogen molecules whose A alpha chains all terminated before A alpha #540-554 were isolated from purified fibrinogen preparations by immunoaffinity chromatography on F-102 Sepharose. Sepharose 184-193 fibrinogen beta chain Homo sapiens 9-19 2403558-14 1990 Affinity chromatography of surface-labeled cell extracts on fibrinogen-Sepharose revealed a 94 +/- 2-kDa membrane protein that bound specifically to fibrinogen-Sepharose only on cells that expressed the MFR. Sepharose 71-80 fibrinogen beta chain Homo sapiens 60-70 2403558-14 1990 Affinity chromatography of surface-labeled cell extracts on fibrinogen-Sepharose revealed a 94 +/- 2-kDa membrane protein that bound specifically to fibrinogen-Sepharose only on cells that expressed the MFR. Sepharose 71-80 fibrinogen beta chain Homo sapiens 149-159 2403558-14 1990 Affinity chromatography of surface-labeled cell extracts on fibrinogen-Sepharose revealed a 94 +/- 2-kDa membrane protein that bound specifically to fibrinogen-Sepharose only on cells that expressed the MFR. Sepharose 160-169 fibrinogen beta chain Homo sapiens 60-70 2403558-14 1990 Affinity chromatography of surface-labeled cell extracts on fibrinogen-Sepharose revealed a 94 +/- 2-kDa membrane protein that bound specifically to fibrinogen-Sepharose only on cells that expressed the MFR. Sepharose 160-169 fibrinogen beta chain Homo sapiens 149-159 2713997-6 1989 Likewise, the isoelectrofocussing of purified non-reduced patient"s fibrinogen in agarose gel showed an abnormal distribution in its focussed bands, especially in a group which focussed in a pI-interval between 5.20-5.85. Sepharose 82-89 fibrinogen beta chain Homo sapiens 68-78 3217923-0 1988 Isolation of fibrinogen A alpha-chain by affinity chromatography on concanavalin A-sepharose. Sepharose 83-92 fibrinogen beta chain Homo sapiens 13-23 3217923-2 1988 A mixture of the three constituent polypeptide chains of human fibrinogen was applied onto a column of concanavalin A-Sepharose. Sepharose 118-127 fibrinogen beta chain Homo sapiens 63-73 3191112-9 1988 When fibrinogen is chromatographed on a column of agarose-bound B beta 15-42, a cation-dependent retention of fibrinogen on the peptide column was observed, and fibrinogen was eluted from the column by B beta 15-42 but not by B beta 1-14. Sepharose 50-57 fibrinogen beta chain Homo sapiens 5-15 3191112-9 1988 When fibrinogen is chromatographed on a column of agarose-bound B beta 15-42, a cation-dependent retention of fibrinogen on the peptide column was observed, and fibrinogen was eluted from the column by B beta 15-42 but not by B beta 1-14. Sepharose 50-57 fibrinogen beta chain Homo sapiens 110-120 3191112-9 1988 When fibrinogen is chromatographed on a column of agarose-bound B beta 15-42, a cation-dependent retention of fibrinogen on the peptide column was observed, and fibrinogen was eluted from the column by B beta 15-42 but not by B beta 1-14. Sepharose 50-57 fibrinogen beta chain Homo sapiens 110-120 3745204-3 1986 Purified human fibrinogen specifically bound to HA-Sepharose to a greater extent (greater than 5-fold) than did alpha 1-acid glycoprotein, DNaseI, ovalbumin, haptoglobin, or lysozyme. Sepharose 51-60 fibrinogen beta chain Homo sapiens 15-25 3366765-7 1988 Electrophoretic light scattering and the binding of type IV collagen by fibrinogen-Sepharose further establish the interaction between type IV collagen and fibrinogen. Sepharose 83-92 fibrinogen beta chain Homo sapiens 72-82 3366765-7 1988 Electrophoretic light scattering and the binding of type IV collagen by fibrinogen-Sepharose further establish the interaction between type IV collagen and fibrinogen. Sepharose 83-92 fibrinogen beta chain Homo sapiens 156-166 3427134-2 1987 The optimal conditions for this binding were elaborated, and the quantitative parameters of Lys-plasminogen binding to fibrinogen-Sepharose were determined. Sepharose 130-139 fibrinogen beta chain Homo sapiens 119-129 2447894-1 1987 A specific antibody population against human fibrinogen was isolated from a rabbit antiserum by affinity chromatography on fibrinogen-bound Sepharose gel. Sepharose 140-149 fibrinogen beta chain Homo sapiens 45-55 2447894-1 1987 A specific antibody population against human fibrinogen was isolated from a rabbit antiserum by affinity chromatography on fibrinogen-bound Sepharose gel. Sepharose 140-149 fibrinogen beta chain Homo sapiens 123-133 3620475-0 1987 Fibrinogen-sepharose interaction with prothrombin, prethrombin 1, prethrombin 2 and thrombin. Sepharose 11-20 fibrinogen beta chain Homo sapiens 0-10 3620475-1 1987 Binding of prothrombin, prethrombin 1, prethrombin 2 and thrombin to fibrinogen-Sepharose was studied. Sepharose 80-89 fibrinogen beta chain Homo sapiens 69-79 3620475-2 1987 Thrombin and prethrombin 2 bound to fibrinogen-Sepharose, while prethrombin 1 and prothrombin did not. Sepharose 47-56 fibrinogen beta chain Homo sapiens 36-46 3620475-4 1987 The affinity of thrombin and prethrombin 2 to fibrinogen-Sepharose depended on ionic strength and reached a maximum at 50 mm concentration. Sepharose 57-66 fibrinogen beta chain Homo sapiens 46-56 3568326-2 1987 The formation of factor XIIIa-catalyzed fibrin polymers during clotting of plasma and purified fibrinogen in vivo was followed by a sodium dodecyl sulfate agarose gel technique, and an increase in both amount and size of gamma-chain cross-linked polymers was demonstrated before visible clot formation. Sepharose 155-162 fibrinogen beta chain Homo sapiens 95-105 3378041-4 1988 Chromatography of the isolated chains of fibrinogen E showed that the alpha(Gly17-Lys78) peptide region itself contains a strong binding site for PMSF-thrombin-Sepharose. Sepharose 160-169 fibrinogen beta chain Homo sapiens 41-51 3590112-1 1987 A study was performed to investigate if protamine covalently attached to CNBr-activated agarose is a useful tool for the purification of fibrinogen from human plasma samples. Sepharose 88-95 fibrinogen beta chain Homo sapiens 137-147 3593282-5 1987 Also, the elution profile of phenylmethane-sulphonyl fluoride-inhibited thrombin from fibrinogen-Sepharose was identical with that of active thrombin from fibrin-monomer-Sepharose. Sepharose 97-106 fibrinogen beta chain Homo sapiens 86-96 3745204-5 1986 Treatment of HA-Sepharose containing bound 125I-fibrinogen with ovine testicular hyaluronidase released 44% of the 125I radioactivity, indicating that fibrinogen was specifically bound to HA. Sepharose 16-25 fibrinogen beta chain Homo sapiens 48-58 3745204-5 1986 Treatment of HA-Sepharose containing bound 125I-fibrinogen with ovine testicular hyaluronidase released 44% of the 125I radioactivity, indicating that fibrinogen was specifically bound to HA. Sepharose 16-25 fibrinogen beta chain Homo sapiens 151-161 3745204-6 1986 Moreover, 125I-fibrinogen bound to HA-Sepharose could be displaced by free HA but not by either of the monosaccharide components of this polymer, glucuronic acid, or N-acetylglucosamine. Sepharose 38-47 fibrinogen beta chain Homo sapiens 15-25 3745204-10 1986 Small HA oligosaccharides (Mr = 3900) were only 50% as effective as larger HA (Mr = 8 X 10(5)) in eluting bound 125I-fibrinogen from HA-Sepharose. Sepharose 136-145 fibrinogen beta chain Homo sapiens 117-127 3745204-12 1986 Additionally, the amount of 125I-fibrinogen bound to HA-Sepharose was directly related to the size of the HA-amine linked to the affinity support. Sepharose 56-65 fibrinogen beta chain Homo sapiens 33-43 3930491-10 1985 TSP binding to fibrinogen-Sepharose occurred in the presence of EDTA, indicating that calcium and magnesium ions are not required for interaction of TSP with fibrinogen. Sepharose 26-35 fibrinogen beta chain Homo sapiens 15-25 3715811-0 1986 Binding properties on Sepharose insolubilized fibrinogen and fibrin, of various species of fibrinogen and fibrin solubilized in plasma. Sepharose 22-31 fibrinogen beta chain Homo sapiens 46-56 3715811-0 1986 Binding properties on Sepharose insolubilized fibrinogen and fibrin, of various species of fibrinogen and fibrin solubilized in plasma. Sepharose 22-31 fibrinogen beta chain Homo sapiens 91-101 3715811-6 1986 Sepharose insolubilized fibrinogen favoured the adsorption of soluble fibrins as compared to fibrinogen in solution; the adsorption of soluble des-AA fibrin was similar to that of soluble des-AABB fibrin. Sepharose 0-9 fibrinogen beta chain Homo sapiens 24-34 3456154-2 1986 The fibrin fragment des-AB N-DSK, which contains the binding sites termed A and B, lost the ability to bind to the site termed a in fibrinogen-Sepharose upon the oxidation of histidine-16 in the B beta chain of fibrinogen [Shimizu, A., Saito, Y., Matsushima, A. Sepharose 143-152 fibrinogen beta chain Homo sapiens 132-142 3456154-2 1986 The fibrin fragment des-AB N-DSK, which contains the binding sites termed A and B, lost the ability to bind to the site termed a in fibrinogen-Sepharose upon the oxidation of histidine-16 in the B beta chain of fibrinogen [Shimizu, A., Saito, Y., Matsushima, A. Sepharose 143-152 fibrinogen beta chain Homo sapiens 211-221 3456154-7 1986 Some of the fragments, which became unable to bind to fibrinogen-Sepharose due to the destruction of site A, however, retained the ability to bind to D-dimer-Sepharose, which contains both sites a and b. Sepharose 65-74 fibrinogen beta chain Homo sapiens 54-64 3930491-11 1985 The binding of TSP to fibrinogen-Sepharose was quantitatively blocked by pretreatment with an antibody to the cyanogen bromide cleavage fragment composed of residues 241-476 of the carboxyl-terminal end of the alpha chain of fibrinogen. Sepharose 33-42 fibrinogen beta chain Homo sapiens 22-32 3930491-11 1985 The binding of TSP to fibrinogen-Sepharose was quantitatively blocked by pretreatment with an antibody to the cyanogen bromide cleavage fragment composed of residues 241-476 of the carboxyl-terminal end of the alpha chain of fibrinogen. Sepharose 33-42 fibrinogen beta chain Homo sapiens 225-235 3930491-13 1985 Excess fibrinogen (30 mg/ml) added to platelet extract quantitatively inhibited binding of TSP to fibrinogen-Sepharose. Sepharose 109-118 fibrinogen beta chain Homo sapiens 7-17 3930491-13 1985 Excess fibrinogen (30 mg/ml) added to platelet extract quantitatively inhibited binding of TSP to fibrinogen-Sepharose. Sepharose 109-118 fibrinogen beta chain Homo sapiens 98-108 4035652-6 1985 Fibrinogen subjected to gelatin-Sepharose chromatography or dialysis against 3.3M urea reacted equivalently with H3. Sepharose 32-41 fibrinogen beta chain Homo sapiens 0-10 4030100-1 1985 Immunochemically identical components were isolated from water-soluble phases of five Staphylococcus aureus strains by affinity chromatography on fibrinogen-linked Sepharose 4B. Sepharose 164-173 fibrinogen beta chain Homo sapiens 146-156 4049326-1 1985 DesAA-fibrin Sepharose was produced by treating fibrinogen-Sepharose with batroxobin. Sepharose 13-22 fibrinogen beta chain Homo sapiens 48-58 4049326-1 1985 DesAA-fibrin Sepharose was produced by treating fibrinogen-Sepharose with batroxobin. Sepharose 59-68 fibrinogen beta chain Homo sapiens 48-58 6441307-0 1984 Specific fibrinogen quantitation by electroimmunodiffusion in agarose gel containing heparin. Sepharose 62-69 fibrinogen beta chain Homo sapiens 9-19 2581874-2 1985 Fibrinogen was isolated from plasmas by affinity chromatography at fibrin monomer Sepharose and characterized by SDS-PAGE. Sepharose 82-91 fibrinogen beta chain Homo sapiens 0-10 6441307-1 1984 In the determination of plasma fibrinogen by electroimmunodiffusion, commercial sodium heparin, previously included in the agarose gel, by interacting with fibrinogen molecules, enhances their anodic mobility more strongly than after carbamylation with potassium cyanate. Sepharose 123-130 fibrinogen beta chain Homo sapiens 156-166 6863272-4 1983 Photooxidation of the activated NH2-terminal disulfide knot, which is derived from fibrin and contains the NH2-terminal binding domain, reduced the ability of this fragment to bind to fibrinogen-Sepharose conjugate. Sepharose 195-204 fibrinogen beta chain Homo sapiens 184-194 6849976-6 1983 In the second series of studies, fibrinogen-Sepharose was prepared and the binding of degradation products directly determined. Sepharose 44-53 fibrinogen beta chain Homo sapiens 33-43 7466316-1 1981 During routine investigation of plasma proteins by agarose gel electrophoresis, a double fibrinogen band was found in a 79-year-old woman without previous history or clinical symptoms of bleeding tendency. Sepharose 51-58 fibrinogen beta chain Homo sapiens 89-99 6890955-5 1982 SK-potentiator showed a similar mobility to that of fibrinogen on both SDS-polyacrylamide gel and agarose gel electrophoresis, and cross-reacted with anti-fibrinogen antiserum. Sepharose 98-105 fibrinogen beta chain Homo sapiens 52-62 7107587-12 1982 Affinity chromatography of the glycopeptides on concanavalin A-Sepharose also showed that the glycopeptides from fibrinogen are greater than 95% biantennary oligosaccharide chains. Sepharose 63-72 fibrinogen beta chain Homo sapiens 113-123 6302680-9 1983 In order to identify the platelet fibrinogen receptor, A2A9 immobilized on agarose was used for affinity chromatography. Sepharose 75-82 fibrinogen beta chain Homo sapiens 34-44 6214865-0 1982 Fractionation of plasmic fibrinogen digest on lysine-agarose. Sepharose 53-60 fibrinogen beta chain Homo sapiens 25-35 79230-1 1978 An assay of human antiplasmins has been developed utilizing radial diffusion of plasma from wells cut in plasmin-enriched, fibrinogen-agarose plates. Sepharose 134-141 fibrinogen beta chain Homo sapiens 123-133 159511-2 1979 Agarose gel filtration of these samples revealed the presence of fibrinogen derivatives both larger and smaller than the parent molecule. Sepharose 0-7 fibrinogen beta chain Homo sapiens 65-75 540036-1 1979 Fibrinogen-fibrin-related antigen (FR antigen) was isolated from as little as 1 ml of human plasma by immuno-affinity chromatography with agarose-bound antibody to human fibrinogen. Sepharose 138-145 fibrinogen beta chain Homo sapiens 0-10 540036-1 1979 Fibrinogen-fibrin-related antigen (FR antigen) was isolated from as little as 1 ml of human plasma by immuno-affinity chromatography with agarose-bound antibody to human fibrinogen. Sepharose 138-145 fibrinogen beta chain Homo sapiens 170-180 706495-3 1978 Finding concerning the interaction of the platelets with fibrinogen connected to sepharose plead for the fact that a change of conformation in the molecule of fibrinogen precedes the specific platelet reaction. Sepharose 81-90 fibrinogen beta chain Homo sapiens 57-67 706495-3 1978 Finding concerning the interaction of the platelets with fibrinogen connected to sepharose plead for the fact that a change of conformation in the molecule of fibrinogen precedes the specific platelet reaction. Sepharose 81-90 fibrinogen beta chain Homo sapiens 159-169 19499-9 1977 Fibrinogen, as assessed by chromatographic experiments with heparin-Sepharose columns, had a considerably lower binding affinity for heparin than did CIg, suggesting that it participates in precipitate formation mainly, if not entirely, by virtue of its affinity for CIg. Sepharose 68-77 fibrinogen beta chain Homo sapiens 0-10 620051-9 1978 Photooxidized fibrinogen has affinity for thrombin-activated fibrinogen-Sepharose and thrombin-activated fragment N-DSK-Sepharose. Sepharose 72-81 fibrinogen beta chain Homo sapiens 14-24 620051-9 1978 Photooxidized fibrinogen has affinity for thrombin-activated fibrinogen-Sepharose and thrombin-activated fragment N-DSK-Sepharose. Sepharose 72-81 fibrinogen beta chain Homo sapiens 61-71 620051-9 1978 Photooxidized fibrinogen has affinity for thrombin-activated fibrinogen-Sepharose and thrombin-activated fragment N-DSK-Sepharose. Sepharose 120-129 fibrinogen beta chain Homo sapiens 14-24 924364-0 1977 Complex formation of crosslinked fibrin oligomers with agarose-coupled fibrinogen and fibrin. Sepharose 55-62 fibrinogen beta chain Homo sapiens 71-81 924364-4 1977 These fractions were subjected to affinity chromatography on agarose-coupled fibrinogen and fibrin. Sepharose 61-68 fibrinogen beta chain Homo sapiens 77-87 810399-1 1975 Human fibrinogen was adsorbed on thrombin-activated fibrinogen which had been immobilized by covalent coupling with Sepharose-6B (Fibrin-Sepharose). Sepharose 116-125 fibrinogen beta chain Homo sapiens 6-16 1036803-2 1976 Eight groups of fibrinogen derivatives could be separated by gel filtration through 6% agarose in large columns, four with an elution volume smaller and four groups with an elution volume larger than that of fibrinogen. Sepharose 87-94 fibrinogen beta chain Homo sapiens 16-26 53064-2 1975 The area of thrombin inactivation is subsequently observed by the coagulation of fibrinogen in a separate agarose gel layer poured over the thrombin gel. Sepharose 106-113 fibrinogen beta chain Homo sapiens 81-91 14416-2 1977 The influence of the pH on the separation of high molecular weight derivatives obtained by a limited action of thrombin on fibrinogen was studied by agarose gel chromatography. Sepharose 149-156 fibrinogen beta chain Homo sapiens 123-133 617780-1 1977 Affinity chromatographic studies using insolubilized fibrinogen (fibrinogen-agarose) revealed that fibrin monomer present in plasma is selectively adsorbed to fibrinogen-agarose and may be quantitatively estimated following desorption. Sepharose 76-83 fibrinogen beta chain Homo sapiens 53-63 617780-1 1977 Affinity chromatographic studies using insolubilized fibrinogen (fibrinogen-agarose) revealed that fibrin monomer present in plasma is selectively adsorbed to fibrinogen-agarose and may be quantitatively estimated following desorption. Sepharose 76-83 fibrinogen beta chain Homo sapiens 65-75 617780-1 1977 Affinity chromatographic studies using insolubilized fibrinogen (fibrinogen-agarose) revealed that fibrin monomer present in plasma is selectively adsorbed to fibrinogen-agarose and may be quantitatively estimated following desorption. Sepharose 76-83 fibrinogen beta chain Homo sapiens 65-75 617780-1 1977 Affinity chromatographic studies using insolubilized fibrinogen (fibrinogen-agarose) revealed that fibrin monomer present in plasma is selectively adsorbed to fibrinogen-agarose and may be quantitatively estimated following desorption. Sepharose 170-177 fibrinogen beta chain Homo sapiens 65-75 617780-1 1977 Affinity chromatographic studies using insolubilized fibrinogen (fibrinogen-agarose) revealed that fibrin monomer present in plasma is selectively adsorbed to fibrinogen-agarose and may be quantitatively estimated following desorption. Sepharose 170-177 fibrinogen beta chain Homo sapiens 65-75 1213264-4 1975 Gel filtration (4% agarose) of the redissolved precipitate resulted in a separation of SFMC and fibrinogen. Sepharose 19-26 fibrinogen beta chain Homo sapiens 96-106 1169259-1 1975 Monovalent goat antibody fragments (Fab) that were monospecific for human fibrinogen were isolated by affinity chromatography on fibrinogen-Sepharose and used as a direct probe for the involvement of fibrinogen in platelet aggregation and the release reaction. Sepharose 140-149 fibrinogen beta chain Homo sapiens 129-139 1169259-1 1975 Monovalent goat antibody fragments (Fab) that were monospecific for human fibrinogen were isolated by affinity chromatography on fibrinogen-Sepharose and used as a direct probe for the involvement of fibrinogen in platelet aggregation and the release reaction. Sepharose 140-149 fibrinogen beta chain Homo sapiens 129-139 810399-1 1975 Human fibrinogen was adsorbed on thrombin-activated fibrinogen which had been immobilized by covalent coupling with Sepharose-6B (Fibrin-Sepharose). Sepharose 116-125 fibrinogen beta chain Homo sapiens 52-62 4258201-0 1971 The identification of fibrinogen derivatives in plasma and serum by agarose gel filtration. Sepharose 68-75 fibrinogen beta chain Homo sapiens 22-32 4216122-0 1974 Characterization of the venoms of various Bothrops species by immunoelectrophoresis and reaction with fibrinogen agarose. Sepharose 113-120 fibrinogen beta chain Homo sapiens 102-112 4216114-0 1973 [Identification and preparation of high-molecular derivatives of fibrinogen from human plasma by means of PAA-gel electrophoresis and agarose-gel chromatography]. Sepharose 134-141 fibrinogen beta chain Homo sapiens 65-75