Arginase 1 (ARG1) Mouse Monoclonal Antibody [Clone ID: UMLBI288]

Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011].

Carrier-free (BSA/glycerol-free) Arginase-1 (ARG1) mouse monoclonal antibody, clone UMLBI288

Arginase, liver; arginase 1; liver-type arginase; OTTHUMP00000017209; type I arginase

Homo sapiens arginase 1 (ARG1), transcript variant 2, mRNA.

383

P05089

Unconjugated

Arginine and proline metabolism, Metabolic pathways

Arginine and proline metabolism, Metabolic pathways

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.

ARG1

https://www.ncbi.nlm.nih.gov/gene/?term=383

https://www.uniprot.org/uniprot/P05089