Responses were correlated to calcium release in cultured rat uterine smooth muscle cells
measured by fluorescence microscopy.
Not exact matches
Energy transfer between the subunits, a
measure of cytosolic cAMP concentration -LRB-[cAMP]-RRB-, and compartmentation of the dissociated subunits were monitored
by confocal
fluorescence microscopy.
By developing a new
fluorescence microscopy - based technique, the researchers were able to
measure how long it takes proteins to move over distances ranging from 0.2 to 3 micrometres in living cells.
We, therefore, treated macrophages of six AD patients and 3 controls
by curcuminoids in vitro and
measured Aβ uptake using
fluorescence and confocal
microscopy.
Several methods to
measure FRET
by fluorescence microscopy can be used, including
fluorescence lifetime imaging, spectral imaging, donor
fluorescence dequenching upon acceptor photobleaching.