GAPDH Polyclonal Antibody, 20ul[BT-AP15693] Centrifuges This gene encodes a member

This gene encodes a member of the fibrillar collagen family

which is known to mediate various intracellular signaling pathways

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

a subpopulation that does not interact with catenins

GAPDH Polyclonal Antibody, 20ul[BT-AP15693] Centrifuges This gene encodes a memberThis 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