PHF8 belongs to the family of ferrous iron and 2-oxoglutarate dependent oxygenases, and is active as a histone lysine demethylase with selectivity for the di-and monomethyl states.Mutations in PHF8 cause Siderius type X-linked mental retardation (XLMR). In addition to moderate mental retardation, features of the Siderius-Hamel syndrome include facial dysmorphism, cleft lip and/or cleft palate, and in some cases microcephaly. A chromosomal microdeletion on Xp11.22 encompassing all of the PHF8 and FAM120C genes and a part of the WNK3 gene was reported in two brothers with autism spectrum disorder in addition to Siderius-type XLMR and cleft lip and palate.
Rat Prolyl hydroxylases (PHD) ELISA Kit employs a two-site sandwich ELISA to quantitate P4HA1 in samples. An antibody specific for P4HA1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyP4HA1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for P4HA1 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 P4HA1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Rat Prolyl hydroxylases (PHD) ELISA Kit 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.
Find more details at http://www.abbkine.com/product/rat-prolyl-hydroxylases-phd-elisa-kit-kte100877/
bio-equip.cn
中文
