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)

SELPLG encodes a glycoprotein that functions as a high affinity counter-receptor for the cell adhesion molecules P-

acetylcholine at neuromuscular junctions and brain cholinergic synapses

Nuclear pore complexes (NPCs) regulate the transport of macromolecules between the nucleus and cytoplasm

Contains 8 LRR (leucine-rich) repeats

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