Detection Method:Sandwich
Test principle:This assay employs a two-site sandwich ELISA to quantitate ZFAND6 in samples. An antibody specific for ZFAND6 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyZFAND6 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for ZFAND6 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 ZFAND6 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview:The deduced 208-amino acid AWP1 protein has a calculated molecular mass of 22.56 kD and shares approximately 55% sequence homology with mouse Awp1 and human ZNF216. AWP1 has 2 conserved zinc finger domains: ZFA20 at its N terminus and ZFAN1 at its C terminus. It contains 2 potential PEST sequences, 4 putative N-glycosylation sites, 7 casein kinase II phosphorylation sites, and 2 N-myristoylation sites. It has a putative nuclear localization signal, but no N-terminal signal peptide, transmembrane domain, or endoplasmic reticulum retention or membrane retention motifs. Northern blot analysis detected ubiquitous expression of a 1.5-kb transcript in all tissues examined, with relatively high levels in heart, skeletal muscle, liver, kidney, and placenta.
