Detection Method:Sandwich
Test principle:This assay employs a two-site sandwich ELISA to quantitate SPR in samples. An antibody specific for SPR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySPR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SPR is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of SPR bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview:Sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase; EC 1.1.1.153) catalyzes the NADPH-dependent reduction of various carbonyl substances, including derivatives of pteridines, and belongs to a group of enzymes called aldo-keto reductases. SPR plays an important role in the biosynthesis of tetrahydrobiopterin (BH4).
The clone encoded a protein of 261 amino acids with a calculated molecular mass of 28,047 Da. The predicted amino acid sequence of human sepiapterin reductase shows 74% identity with the rat enzyme and a striking homology with human carbonyl reductase, estradiol 17-beta-dehydrogenase, and 3-beta-hydroxy-5-ene steroid dehydrogenase, especially in the N-terminal region.
