GPX3 Polyclonal Antibody, 100ul Sealing Film Defects in this gene are

Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC)

making it possible to observe cells clearly under light microscopes and fluorescence microscopes

has two repeats of quasi-RRM (RNA recognition motif) domains that bind to RNAs

acetylcholine at neuromuscular junctions and brain cholinergic synapses

This protein is thought to contribute to the transformed phenotype of T cells after infection by herpesvirus samimiri

GPX3 Polyclonal Antibody, 100ul Sealing Film Defects in this gene areThe protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of organic hydroperoxides and hydrogen peroxide (H2O2) by glutathione, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme is secreted, and is abundantly found in plasma. Downregulation of expression of