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Arginase-1 (ABT-Arg1) mouse mAb

货号: YP-Ab-18163
促销价:

产品介绍

反应种属
Human
应用范围
IHC;WB;IF;ELISA
抗体类型
单克隆抗体
基因名称(Gene Name)
ARG1
蛋白名称
Arginase-1 (EC 3.5.3.1) (Liver-type arginase) (Type I arginase)
分子量(DA)
35kD
免疫原
Synthesized peptide derived from human Arginase-1 AA range: 200-322
特异性
The antibody can specifically recognize human Arginase-1 protein. In western blotting of HepG2 cell lysate, the antibody can label a 35 kDa band corresponding to Arginase-1.
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
来源
Mouse, Monoclonal/IgG2b, kappa
稀释比例
IHC 1:200-1000. WB 1:500-2000. IF 1:100-500. ELISA 1:1000-5000
纯化工艺
Protein G
浓度
1 mg/ml
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
其他名称
背景
Arginase-1 is a key enzyme in the urea cycle, which can catalyze the decomposition of arginine into ornithine and urea. Highly specific expression in liver tissue, but not in bile duct epithelial cells, hepatic sinusoidal endothelial cells, Kupffer cells and vascular endothelial cells.
功能
catalytic activity:L-arginine + H(2)O = L-ornithine + urea.,cofactor:Binds 2 manganese ions per subunit.,disease:Defects in ARG1 are the cause of argininemia (ARGIN) [MIM:207800]; also known as hyperargininemia. Argininemia is a rare autosomal recessive disorder of the urea cycle. Arginine is elevated in the blood and cerebrospinal fluid, and periodic hyperammonemia occurs. Clinical manifestations include developmental delay, seizures, mental retardation, hypotonia, ataxia, progressive spastic quadriplegia.,induction:By arginine or homoarginine.,online information:Arginase entry,pathway:Nitrogen metabolism; urea cycle; L-ornithine and urea from L-arginine: step 1/1.,similarity:Belongs to the arginase family.,subunit:Homotrimer.,

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