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Time resolved-FRET signal

Fluorescence-based detection methods are the most commonly used readouts for HTS as these readouts are sensitive, usually homogeneous and can be readily miniaturised, even down to the single molecule level.7,8 Fluorescent signals can be detected by methods such as fluorescence intensity (FI), fluorescence polarisation (FP) or anisotropy (FA), fluorescence resonance energy transfer (FRET), time-resolved fluorescence resonance energy transfer (TR-FRET) and fluorescence intensity life time (FLIM). Confocal single molecule techniques such as fluorescence correlation spectroscopy (FCS) and one- or two-dimensional fluorescence intensity distribution analysis (ID FID A, 2D FIDA) have been reported but are not commonly used. [Pg.249]

Time-resolved fluorescence Z -LYTE A site-specific protease recognizes and cleaves non-phosphorylated ERET-peptides. Cleavage disrupts FRET signals, whereas uncleaved, phosphorylated ERET-peptides maintain ERET High... [Pg.330]


See other pages where Time resolved-FRET signal is mentioned: [Pg.90]    [Pg.599]    [Pg.376]    [Pg.423]    [Pg.927]    [Pg.6]    [Pg.26]    [Pg.5]    [Pg.167]    [Pg.167]    [Pg.243]    [Pg.15]    [Pg.361]    [Pg.454]    [Pg.335]    [Pg.373]    [Pg.377]    [Pg.111]    [Pg.168]    [Pg.127]    [Pg.59]    [Pg.74]   
See also in sourсe #XX -- [ Pg.599 ]




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