
pmid: 23093350
AbstractIn this unit on fluorescence recovery after photobleaching (FRAP), an imaging approach to study protein‐protein interactions in situ is described. The protocols presented use confocal microscopy to examine the mobility of a fluorescent protein by measuring the recovery of the protein in a bleached area. The data gained in FRAP studies is qualitative and yields insight into relative binding affinity, binding characteristics, and the effect of treatments or mutations on protein mobility. Curr. Protoc. Neurosci. 61:2.17.1‐2.17.12. © 2012 by John Wiley & Sons, Inc.
Microscopy, Confocal, Time Factors, actins, GFPactin cytoskeleton, Green Fluorescent Proteins, fluorescence recovery after photobleaching, Neurosciences, time factors, Actins, Actin Cytoskeleton, confocal, Neurology, FRAP, microscopy, Medicine and Health Sciences, cells, cultured, green fluorescent proteins, actin, protein mobility, Cells, Cultured, Fluorescence Recovery After Photobleaching
Microscopy, Confocal, Time Factors, actins, GFPactin cytoskeleton, Green Fluorescent Proteins, fluorescence recovery after photobleaching, Neurosciences, time factors, Actins, Actin Cytoskeleton, confocal, Neurology, FRAP, microscopy, Medicine and Health Sciences, cells, cultured, green fluorescent proteins, actin, protein mobility, Cells, Cultured, Fluorescence Recovery After Photobleaching
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