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ARG1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 5D6D12, Proteintech
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Arginase-1 (ARG1) catalyzes the hydrolysis of L-arginine into ornithine and urea, a critical step for the urea cycle. Defects in ARG1 are the cause of argininemia, an autosomal recessive disorder characterized by hyperammonemia. There are several isoforms of mammalian arginase. The type I isoform, is a cytosolic enzyme and expressed predomitly in the liver as a component of the urea cycle. Hepatocellular carcinoma usually shows higher protein expression of ARG1 than normal liver cells.
Specifications
Specifications
| Antigen | ARG1 |
| Applications | Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot |
| Classification | Monoclonal |
| Clone | 5D6D12 |
| Concentration | 1 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 |
| Gene | ARG1 |
| Gene Accession No. | P05089, P07824, Q61176, Q95JC8 |
| Gene Alias | ARG1, Arginase 1, liver Arginase, Liver type arginase |
| Show More |
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