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.

推荐稀释比 WB:1/1000-1/2000; IP:1/50

Western blot analysis of ARG1 in mouse liver lysates using Liver Arginase antibody.

-25 ~ -15℃保存，收到货之后有效期1年，避免反复冻融。