GAPDH Monoclonal Antibody(2B8), 50ul[BT-MCA0039] Bottle-Top Dispenser With Other Brain Malformations 8

With Other Brain Malformations 8 and Optic Nerve Hypoplasia

a single pass transmembrane region

Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C

This gene belongs to the amiloride-sensitive Na+ channel and degenerin (NaC/DEG) family

integrin complexes mediate cell-cell and cell-extracellular matrix interactions and this complex plays a role in human airway epithelial proliferation

GAPDH Monoclonal Antibody(2B8), 50ul[BT-MCA0039] Bottle-Top Dispenser With Other Brain Malformations 8This gene encodes a member of the glyceraldehyde 3 phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde 3 phosphate in the presence of inorganic phosphate and nicotinamide