Ornithine Carbamoyltransferase (OTC) Mouse Monoclonal Antibody [Kloon ID: LBI5A7]

This nuclear gene encodes a mitochondrial matrix enzyme. Missense, nonsense, and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. Since the gene for this enzyme maps close to that for Duchenne muscular dystrophy, it may play a role in that disease also. [provided by RefSeq, Jul 2008]

Carrier-free (BSA/glycerol-free) OTC mouse monoclonal antibody, clone LBI5A7

OCTD; OTCD

Homo sapiens ornithine transcarbamylase (OTC), mRNA; nuclear gene for mitochondrial product.

5009

P00480

Unconjugated

Arginine and proline metabolism, Metabolic pathways

Arginine and proline metabolism, Metabolic pathways

WB 1:2000, IHC 1:150

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.

OTC

https://www.ncbi.nlm.nih.gov/gene/?term=5009

https://www.uniprot.org/uniprot/P00480