ALDH4A1 Mouse Monoclonal Antibody [Kloon ID: LBI1H10]

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. [provided by RefSeq, Jun 2009]

Carrier-free (BSA/glycerol-free) ALDH4A1 mouse monoclonal antibody, clone LBI1H10

ALDH4; P5CD; P5CDh

Homo sapiens aldehyde dehydrogenase 4 family member A1 (ALDH4A1), transcript variant 3, mRNA; nuclear gene for mitochondrial product.

8659

P30038

Unconjugated

Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways

Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways

WB 1:500, IHC 1:500

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

ALDH4A1

https://www.ncbi.nlm.nih.gov/gene/?term=8659

https://www.uniprot.org/uniprot/P30038