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Fluorescence protection immunoassay

The hydrolysis of a nonfluorescent enzyme substrate to a fluorescent product is widely utilized to measure the activity of a large number of enzymes. Binding of enzyme substrates by antibodies often protects the enzymatically labile bond from hydrolysis. By the combination of these two formats, the substrate-labeled fluorescent immunoassay (SLFIA) was developed. ... [Pg.276]

Fluorescence Protection Immunoassay (Indirect Fluorescence Quenching... [Pg.61]

Cullum, M. E. Hine, R Simonson, L. G. Shih, C. N. Bienek, D. R. Park, S. Ragain, J. C. Rapid competitive fluorescence-polarization immunoassay of anthrax protective antigen in vaccine cultures and bodily fluids. U.S. Pat. Appl. Publ. US 2004235075, 2004 Chem. Abstr. 2004,142, 19550. [Pg.292]

Maragos CM, Kim EK. Detection of zearalenone and related metabolites by fluorescence polarization immunoassay. J Food Protect 2004 67 1039-43. [Pg.430]

See other pages where Fluorescence protection immunoassay is mentioned: [Pg.212]    [Pg.278]    [Pg.71]    [Pg.84]    [Pg.27]    [Pg.858]    [Pg.468]    [Pg.370]    [Pg.466]    [Pg.473]    [Pg.27]    [Pg.548]    [Pg.110]    [Pg.229]    [Pg.396]    [Pg.528]    [Pg.335]    [Pg.70]    [Pg.445]    [Pg.475]    [Pg.1238]    [Pg.161]    [Pg.162]    [Pg.748]   
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