Detection Method:Sandwich
Test principle:This assay employs a two-site sandwich ELISA to quantitate ABCC10 in samples. An antibody specific for ABCC10 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyABCC10 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for ABCC10 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 ABCC10 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview:Members of the ABC family of membrane proteins, such as ABCC10, are involved in energy-dependent transport of a wide variety of substrates across membranes. The 1,492-amino acid ABCC10 protein has a calculated molecular mass of 162 kD. It contains 2 nucleotide-binding folds, 17 predicted transmembrane segments arranged in 3 transmembrane domains, and 3 predicted N-glycosylation sites. Northern blot analysis was unable to detected ABCC10 expression, but RT-PCR detected ABCC10 expression in all 10 tissues examined. In vitro-translated ABCC10 had an apparent molecular mass of 158 kD by SDS-PAGE.Basal MRP7 promoter activity relied upon a proximal segment of the 5-prime flanking region bearing an E2F site acting cooperatively with 2 closely positioned SP1 sites.
