Fluo-3 absorbs at approximately 506 nm and emits at 526 nm when bound to calcium. In the absence of calcium it is practically non-fluorescent. The higher Kd and longer excitation wavelength of Fluo-3 can have significant advantages over other indicators because of the reduced interference with sample autofluorescence. It demonstrates efficient excitation with laser-based instrumentation, including confocal laser scanning microscopes. It has been widely used for flow cytometry and is one of the imaging methods of intracellular calcium flux that is associated with GPCR dynamics.
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