AGTR2 Polyclonal Antibody, 50ul NGS Oligos hydrophobic C-terminal domain with a

hydrophobic C-terminal domain with a steroid substrate binding site

GTP-bound G alpha subunits and acting as a GTPase activating protein (GAP)

Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy

With a capacity of 100-1000μl and DNase/RNase-free properties

TPH1 encodes a member of the aromatic amino acid hydroxylase family

AGTR2 Polyclonal Antibody, 50ul NGS Oligos hydrophobic C-terminal domain with aThe protein encoded by this gene belongs to the G protein coupled receptor 1 family, and functions as a receptor for angiotensin II. It is an intergral membrane protein that is highly expressed in fetus, but scantily in adult tissues, except brain, adrenal medulla, and atretic ovary. This receptor has been shown to mediate programmed cell death and this apoptotic function may play an important role in developmental biology and pathophysiology.