<p>In Binding Diffusion* (14), <i>c</i><sub><i>k</i></sub> represents the concentration of ligand receptor complex in the <i>k</i>th image, </p><p></p><p></p><p><mi>c</mi><mi>k</mi><mi>M</mi></p><p></p><p></p> is the mobile fraction of <i>c</i>, <i>β</i> is the immobile fraction, and <i>τ</i> is the time needed for each image scan. Finally, <i>g</i><sub>1</sub> and <i>g</i><sub>2</sub> are the bleaching functions for bounded (<i>c</i>) and free (<i>u</i>) proteins.<p></p
Fluorescence recovery after photobleaching (FRAP) is a common experimental method for investigating ...
Fluorescence recovery after photobleaching (FRAP) is one of the most widely used approaches to quant...
AbstractFluorescence recovery after photobleaching (FRAP) is now widely used to investigate binding ...
Fluorescence recovery after photobleaching is a widely established method for the estimation of diff...
Fluorescence Recovery After Photobleaching (FRAP) has been a versatile tool to study transport and r...
AbstractMost of the important types of interactions that occur in cells can be characterized as bind...
The immunological synapse is a stable intercellular structure that specializes in substance and sign...
The fluorescence recovery after photobleaching (FRAP) technique has been used for decades to measure...
Fluorescence recovery after photobleaching (FRAP) is a versatile tool for determining diffusion and ...
Kinetic rates and binding affinity of receptor-ligand interactions are important determinants of cel...
Fluorescence recovery after photobleaching (FRAP) is a versatile tool for determining diffusion and ...
Protein lateral mobility in cell membranes is generally measured using fluorescence photobleaching r...
International audienceFluorescence recovery after photobleaching (FRAP) is a standard method used to...
AbstractKinetic rates and binding affinity of receptor-ligand interactions are important determinant...
<p>FRAP data with photofading (•) were simulated using <i>f</i><sub><i>dADaM</i><sub><i>f</i></sub><...
Fluorescence recovery after photobleaching (FRAP) is a common experimental method for investigating ...
Fluorescence recovery after photobleaching (FRAP) is one of the most widely used approaches to quant...
AbstractFluorescence recovery after photobleaching (FRAP) is now widely used to investigate binding ...
Fluorescence recovery after photobleaching is a widely established method for the estimation of diff...
Fluorescence Recovery After Photobleaching (FRAP) has been a versatile tool to study transport and r...
AbstractMost of the important types of interactions that occur in cells can be characterized as bind...
The immunological synapse is a stable intercellular structure that specializes in substance and sign...
The fluorescence recovery after photobleaching (FRAP) technique has been used for decades to measure...
Fluorescence recovery after photobleaching (FRAP) is a versatile tool for determining diffusion and ...
Kinetic rates and binding affinity of receptor-ligand interactions are important determinants of cel...
Fluorescence recovery after photobleaching (FRAP) is a versatile tool for determining diffusion and ...
Protein lateral mobility in cell membranes is generally measured using fluorescence photobleaching r...
International audienceFluorescence recovery after photobleaching (FRAP) is a standard method used to...
AbstractKinetic rates and binding affinity of receptor-ligand interactions are important determinant...
<p>FRAP data with photofading (•) were simulated using <i>f</i><sub><i>dADaM</i><sub><i>f</i></sub><...
Fluorescence recovery after photobleaching (FRAP) is a common experimental method for investigating ...
Fluorescence recovery after photobleaching (FRAP) is one of the most widely used approaches to quant...
AbstractFluorescence recovery after photobleaching (FRAP) is now widely used to investigate binding ...