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• W2171922654 abstract "Membrane domains, such as caveolae and clathrin-coated pits, regulate cell signaling and protein internalization in the plasma membrane. Fluorescence imaging and microscopy provide an opportunity to determine the receptor protein dynamics of membrane microdomains. The family of image correlation spectroscopy (ICS) techniques provides powerful tools with which to measure the aggregation, clustering, and dynamics of proteins in the plasma membrane. ICS is used to calculate the cluster density and the degree of aggregation of plasma membrane proteins, whereas image cross-correlation spectroscopy (ICCS) measures the fraction of colocalization of two proteins. Dynamic image correlation spectroscopy (DICS) can be used to analyze protein dynamics on the cell surface during live-cell imaging." @default.
• W2171922654 created "2016-06-24" @default.
• W2171922654 creator A5013661873 @default.
• W2171922654 creator A5044713611 @default.
• W2171922654 date "2007-12-18" @default.
• W2171922654 modified "2023-10-18" @default.
• W2171922654 title "Image Correlation Spectroscopy" @default.
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• W2171922654 doi "https://doi.org/10.1126/stke.4172007pl7" @default.
• W2171922654 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18089858" @default.
• W2171922654 hasPublicationYear "2007" @default.
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