ADT2 Polyclonal Antibody, 50ul Cell fragmentation and collection Defects in this gene cause

Defects in this gene cause familial adenomatous polyposis (FAP)

an autosomal dominant disorder

Diameter × depth : 8 x 26mm

This gene encodes a subunit of the heterotetrameric adaptor-related protein comlex 3 (AP-3)

Plays a role in blood glucose homeostasis contributing to the insulin secretion response by pancreatic beta cells

ADT2 Polyclonal Antibody, 50ul Cell fragmentation and collection Defects in this gene causeThis gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Suppressed expression of this gene has been shown to induce apoptosis and inhibit tumor growth. The human