PRODH Mouse Monoclonal Antibody [Kloon ID: LBI1H6]

This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4) . This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]

Carrier-free (BSA/glycerol-free) PRODH mouse monoclonal antibody, clone LBI1H6

HSPOX2; PIG6; POX; PRODH1; PRODH2; TP53I6

Homo sapiens proline dehydrogenase 1 (PRODH), transcript variant 1, mRNA; nuclear gene for mitochondrial product.

5625

O43272

Unconjugated

Arginine and proline metabolism, Metabolic pathways

Arginine and proline metabolism, Metabolic pathways

WB 1:2000, 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.

PRODH

https://www.ncbi.nlm.nih.gov/gene/?term=5625

https://www.uniprot.org/uniprot/O43272