kinetics neo 2.5 software package Search Results


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Biacore 3000 bioevaluation software program package
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
3000 Bioevaluation Software Program Package, supplied by Biacore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biacore biacore t100 evaluation software
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
Biacore T100 Evaluation Software, supplied by Biacore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad icycler iq real time pcr detection system
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
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FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
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FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
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NETZSCH advanced thermokinetic software package kinetics neo
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
Advanced Thermokinetic Software Package Kinetics Neo, supplied by NETZSCH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GraphPad Software Inc michaelis–menten enzyme kinetic model
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
Michaelis–Menten Enzyme Kinetic Model, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad kinetic software
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
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KinetX Inc uncertainty-aware kinetic-modeling program
FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore <t>3000.</t> In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.
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FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore 3000. In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.

Journal: Journal of Biological Chemistry

Article Title: Mapping of a Conformational Epitope on Plasminogen Activator Inhibitor-1 by Random Mutagenesis

doi: 10.1074/jbc.m208420200

Figure Lengend Snippet: FIG. 6. Real time affinity binding of active and latent PAI-1 to 33B8 (panel A) or to control monoclonal antibody 31C9 (panel B). Binding was measured by SPR with a biosensor BIAcore 3000. In each case 62 nM of purified active or latent PAI-1 in HBS-P buffer (pH 7.4) was analyzed on a CM 5 chip with amine-coupled murine 33B8 and 31C9 at a flow rate of 20 l/min at 25 °C. The binding association and dissociation phases were monitored for 3 min, then the chip surface was regenerated by a 20-l pulse of 10 mM glycine (pH 1.5) after each injection. The SPR response of control activated surfaces without anti- bodies or with mouse Fc fragments was subtracted from each curve.

Article Snippet: All measurements were performed at 25 °C, and BIAcore 3000 Bioevaluation software program package (BIAcore AB) was used for analysis of data.

Techniques: Binding Assay, Control, Purification, Injection