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. [provided by RefSeq].
Alternative names: ARG1; OTTHUMP00000017209; Arginase 1; liver-type arginase; type I arginase; arginase, liver.
| Product Name: | Anti-ARG1 Antibody |
|---|---|
| Reference #: | CE00080 |
| Clone #: | 4E6 |
| Source #: | Mouse Monoclonal |
| Reactivity: | Human |
| Catalog Number & Aliquote Size #: |
C0080MA01-MA | 0.1 mL C0080MA05-MA | 0.5 mL C0080MA10-MA | 1.0 mL |
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