Antibodies that bind to target receptors on the cell surface can confer conformation and clustering alterations. These dynamic changes have implications for characterizing drug development in target cells. This protocol utilizes confocal microscopy and image correlation spectroscopy through ImageJ/FIJI to quantify the extent of receptor clustering on the cell surface.
Here, we demonstrate a protocol to use 16α-[18F]-fluoro-17β-estradiol (18F-FES) positron emission tomography (PET) as a tool to visualize ERα expression in ERα-positive breast xenografts.
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