<p>Analytical conditions: PBS, 25°C. <i>k</i><sub>a</sub>: association rate constant, <i>k</i><sub>d</sub>: dissociation rate constant, K<sub>D</sub>: dissociation constant, R<sub>max</sub>: maximum binding amount. RU: resonance unit. 1 RU = 1 pg/mm<sup>2</sup>.</p
Reversible, noncovalent binding is the first obligatory step in the expression of the function of mo...
The influence of drug-receptor binding kinetics has often been overlooked during the development of ...
The reversible combination of a ligand with specific sites on the surface of a receptor is one of th...
<p>Association rate constants (k<sub>a</sub>), dissociation rate constants (k<sub>d</sub>), equilibr...
<p>a: The association rate constant (<i>K</i>a) is here defined as the rate of complex formation per...
The development of ruthenium-based complexes for cancer treatment requires a variety of pharmacologi...
<p>(est): Binding rates were calculated by separately fitting association and dissociation rate cons...
<p>The K<sub>on</sub> (calculated on rate), K<sub>off</sub> (observed off rate), t<sub>1/2</sub> (ha...
Fast kinetic methods are used to measure reactions that take place in less time than required to mix...
<div><p>The prediction of protein-protein kinetic rate constants provides a fundamental test of our ...
The prediction of protein-protein kinetic rate constants provides a fundamental test of our understa...
<p>Kinetic constants of interaction between GFP-ready-TNFα and GFP variants, determined by interfero...
Drug-receptor interaction plays an important role in a series of biological effects, such as cell pr...
<p>Ka and Kd are rate constants for association and dissociation respectively; KD is the equilibrium...
<p>Ligand FlhA<sub>C</sub> was exposed to 2, 1, 0.5, 0.25 and 0.125 μM FlhB<sub>C</sub>. A, associat...
Reversible, noncovalent binding is the first obligatory step in the expression of the function of mo...
The influence of drug-receptor binding kinetics has often been overlooked during the development of ...
The reversible combination of a ligand with specific sites on the surface of a receptor is one of th...
<p>Association rate constants (k<sub>a</sub>), dissociation rate constants (k<sub>d</sub>), equilibr...
<p>a: The association rate constant (<i>K</i>a) is here defined as the rate of complex formation per...
The development of ruthenium-based complexes for cancer treatment requires a variety of pharmacologi...
<p>(est): Binding rates were calculated by separately fitting association and dissociation rate cons...
<p>The K<sub>on</sub> (calculated on rate), K<sub>off</sub> (observed off rate), t<sub>1/2</sub> (ha...
Fast kinetic methods are used to measure reactions that take place in less time than required to mix...
<div><p>The prediction of protein-protein kinetic rate constants provides a fundamental test of our ...
The prediction of protein-protein kinetic rate constants provides a fundamental test of our understa...
<p>Kinetic constants of interaction between GFP-ready-TNFα and GFP variants, determined by interfero...
Drug-receptor interaction plays an important role in a series of biological effects, such as cell pr...
<p>Ka and Kd are rate constants for association and dissociation respectively; KD is the equilibrium...
<p>Ligand FlhA<sub>C</sub> was exposed to 2, 1, 0.5, 0.25 and 0.125 μM FlhB<sub>C</sub>. A, associat...
Reversible, noncovalent binding is the first obligatory step in the expression of the function of mo...
The influence of drug-receptor binding kinetics has often been overlooked during the development of ...
The reversible combination of a ligand with specific sites on the surface of a receptor is one of th...