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.

WB: 1/500-1/1000  IHC: 1/50-1/100  IF: 1/50-1/200  IP: 1/30  

Western

Western blot analysis of Liver Arginase in (1) Human fetal liver lysates; (2) Human fetal lung lysates using Liver Arginase antibody.

Immunohistochemistry

Immunohistochemistry analysis of paraffin-embedded Human liver using Liver Arginase antibody.High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。