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Anal Biochem ; 202(1): 6-9, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1320351

ABSTRACT

An enzymatic cycling procedure for beta-NADP+ generated by the enzyme 3'-phosphodiesterase, 2':3'-cyclic nucleotide (EC 3.1.4.37) from its substrate 2':3'-cyclic NADP+ is described. The enzymes glucose-6-phosphate dehydrogenase (EC 1.1.1.49) and diaphorase (EC 1.8.1.4) are used to cycle the cofactor between its oxidized and reduced forms in the presence of glucose-6-phosphate and p-iodonitrotetrazolium violet (INT) with the concomitant production of colored INT-formazan, monitored at 492 nm. The amplification is about 400-fold per hour and is sensitive enough to detect 6 x 10(-13) mol of NADP(H). A simple procedure for the optimization of this cycling assay is also described. Conjugates to 3'-phosphodiesterase, 2':3'-cyclic nucleotide may be used in heterogeneous enzyme immunoassays for the detection of small quantities of haptens or proteins in biological fluids.


Subject(s)
2',3'-Cyclic-Nucleotide Phosphodiesterases/metabolism , NADP/metabolism , Phosphoric Diester Hydrolases , 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase , Dihydrolipoamide Dehydrogenase/metabolism , Glucosephosphate Dehydrogenase/metabolism , Kinetics , Oxidation-Reduction , Sensitivity and Specificity , Spectrophotometry, Ultraviolet , Tetrazolium Salts/chemistry
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