Detection Method:Sandwich
Test principle:This assay employs a two-site sandwich ELISA to quantitate PRUNE2 in samples. An antibody specific for PRUNE2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRUNE2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PRUNE2 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 PRUNE2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview:The deduced 2,714-amino acid protein has a coiled-coil sequence, a proline-rich region, a P loop, and a C-terminal BNIP2 and CDC42GAP (ARHGAP1) homology (BCH) domain, which contains 3 putative transmembrane domains. Northern blot analysis detected a 12-kb transcript in fetal brain. Semiquantitative RT-PCR revealed BMCC1 expression in all tissues examined except bone marrow, thymus, and spleen.
Expression was highest in brain, cerebellum, spinal cord, and adrenal gland. RT-PCR of synchronized HeLa cells showed that BMCC1 was predominantly expressed in G1 phase of the cell cycle. In situ hybridization of mouse embryos showed that Bmcc1 was specifically expressed in neural tube and neural crest-related tissues.
