Rat UDP-glucumno-syltransferase 1 (UGT1) ELISA Kit

UGT1A10 encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has glucuronidase activity on mycophenolic acid, coumarins, and quinolines.

UGT1A1; GNT1; HUG-BR1; UDPGT; UGT1; UGT1A; UDP glucuronosyltransferase 1A1; UDP glycosyltransferase 1 family; polypeptide A1; bilirubin UDP-glucuronosyltransferase 1-1; bilirubin UDP-glucuronosyltransferase is

The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Rat UDP-glucumno-syltransferase 1 (UGT1) ELISA Kit has high sensitivity and excellent specificity for detection of Rat UGT1A1. No significant cross-reactivity or interference between Rat UGT1A1 and analogues was observed.

This Rat UDP-glucumno-syltransferase 1 (UGT1) ELISA Kit employs a two-site sandwich ELISA to quantitate UGT1A1 in samples. An antibody specific for UGT1A1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyUGT1A1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for UGT1A1 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 UGT1A1 bound in the initial step. The color development is stopped and the intensity of the color is measured.

UGT1A1; GNT1; HUG-BR1; UDPGT; UGT1; UGT1A; UDP glucuronosyltransferase 1A1; UDP glycosyltransferase 1 family; polypeptide A1; bilirubin UDP-glucuronosyltransferase 1-1; bilirubin UDP-glucuronosyltransferase is

• Do not mix components from different kit lots or use reagents beyond the kit expiration date.• Allow all reagents to warm to room temperature for at least 30 minutes before opening.• Pre-rinse the pipet tip with reagent, use fresh pipet tips for each sample, standard and reagent to avoid contamination.• Unused wells must be kept desiccated at 4 °C in the sealed bag provided.• Mix Thoroughly is very important for the result. It is recommended using low frequency oscillator or slight hand shaking every 10 minutes.• It is recommended that all samples and standards be assayed in duplicate or triplicate.