Arginase 1 Mouse anti-Human, Clone: 658934, Invitrogen
Mouse Monoclonal Antibody
Manufacturer: Invitrogen MA524298
Reconstitute at 0.5 mg/mL in sterile PBS.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.
|PBS with 5% trehalose and No Preservative|
|arginase-1, liver-type arginase, type I arginase|
|-20° C, Avoid Freeze/Thaw Cycles|
|Immunoprecipitation, Western Blot|
|E. coli-derived recombit human Arginase 1/ARG1 Met1-Lys322|
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