KIR3.3 Polyclonal Antibody, 20ul NGS Oligos Mutations in this gene cause

Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD)

Each chain contains a collagen-like region located near the N-terminus

ACTBL2 (Actin

Alternatively spliced transcript variants encoding multiple isoforms have been observed for MED27

KIR3.3 Polyclonal Antibody, 20ul NGS Oligos Mutations in this gene causePotassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by KCNJ9 is an integral membrane protein and inward rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G proteins. It associates with another G protein activated potassium channel to form a