AL4A1 Rabbit Polyclonal Antibody, 100ul Shakers PRPF31 encodes a component of

PRPF31 encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes

COL4A3 is also linked to an autosomal recessive form of Alport syndrome

average spacing of wire column: 260 µm

Pimase (DNA) subunit 1 ncoded by PRIM1 is the small

This protein is thought to play an important role in glucose homeostasis by regulating the insulin-dependent trafficking of the glucose transporter 4 (GLUT4)| important for removing glucose from the bloodstream into skeletal muscle and fat tissues

AL4A1 Rabbit Polyclonal Antibody, 100ul Shakers PRPF31 encodes a component ofThis protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline 5 carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta 1 pyrroline 5 carboxylate (P5C) and proline. Alternatively