GAPDH Polyclonal Antibody, 20ul[BT-AP15693] Centrifuges Mutations in this gene are

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

This gene encodes a member of the fibrillar collagen family

which is known to mediate various intracellular signaling pathways

The phosphorylation of the complex by CDC2 kinase reduces the helicase activity

ADRA1A encodes alpha-1A-adrenergic receptor

GAPDH Polyclonal Antibody, 20ul[BT-AP15693] Centrifuges Mutations in this gene areThis 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