PPP1R3A Polyclonal Antibody, 100ul General Lab Use The genome has two identical

The genome has two identical copies of this gene within a palindromic region

Disruption of VEGFA in mice resulted in abnormal embryonic blood vessel formation

Mutations in this gene cause Griscelli syndrome type-1 (GS1)

CLDN2 (claudin 2) product belongs to the claudin protein family whose members have been identified as major integral membrane proteins localized exclusively at tight junctions

This gene encodes a preproprotein that is proteolytically processed to generate multiple protein products

PPP1R3A Polyclonal Antibody, 100ul General Lab Use The genome has two identicalThe glycogen associated form of protein phosphatase 1 (PP1) derived from skeletal muscle is a heterodimer composed of a 37 kD catalytic subunit and a 124 kD targeting and regulatory subunit. PPP1R3A (protein phosphatase 1 regulatory subunit 3A) encodes the regulatory subunit which binds to muscle glycogen with high affinity, thereby enhancing dephosphorylation of glycogen bound substrates for PP1 such as glycogen synthase and glycogen phosphorylase