AL4A1

BT-AP01547

Rabbit

IgG

100ul,50ul,20ul

Polyclonal

Synthesized peptide derived from human AL4A1

The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.103% sodium azide.

-20°C for 1 year

This 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 spliced transcript variants encoding different isoforms have been identified for this gene.

Human: P30038; Mouse: Q8CHT0; Rat: P0C2X9;

Human: 8659; Mouse: 212647; Rat: 0

AL4A1; Delta-1-pyrroline-5-carboxylate dehydrogenase; mitochondrial; P5C dehydrogenase; EC 1.5.1.12; Aldehyde dehydrogenase family 4 member A1)

Metabolism; Signal transduction; Tags & cell markers

ALDH4A1