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重组人Arginase-1/ARG1 Protein(C-6His)

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产品名称: 重组人Arginase-1/ARG1 Protein(C-6His)
产品型号: PN100102-50ug
产品展商: PERFEMIKER
产品价格: 4320.00 元
会员价格: 0.00 元
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简单介绍

重组人Arginase-1/ARG1 Protein(C-6His) 货号:PN100102 规格:50ug; 标签:C-6His; 来源:Human; 表达宿主:Human cells


重组人Arginase-1/ARG1 Protein(C-6His)  的详细介绍

名称:重组人Arginase-1/ARG1 Protein(C-6His);


产品说明(Description)
Recombinant Human Arginase-1 is produced by our Mammalian expression system and the target gene encoding Met1-Lys322 is expressed with a 6His tag at the C-terminus. 
Accession #: P05089
Known as: Arginase-1; Liver-type arginase; Type I arginase; ARG1

制剂(Formulation)
Supplied as a 0.2 μm filtered solution of 20mM Tris, 150mMNaCl, 20%Glycerol,1mMDTT,pH7.4.

质量控制(Quality Control) 
Purity: Greater than 90% as determined by reducing SDS-PAGE.    
Endotoxin: Less than 0.1 ng/ug (1 IEU/ug) as determined by LAL test.

复溶(Reconstitution)

保存(Storage)
Store at < -20°C, stable for 6 months after receipt.Please minimize freeze-thaw cycles.   

背景(Background)
ARG1 is a member of the ureohydrolase family of enzymes. ARG1 can catalyze the hydrolysis of arginine to ornithine and urea. In the urea cycle, ARG1 catalyzes the fifth and final step, a series of biochemical reactions in mammals during which the body disposes of harmful ammonia. ARG1 is a cytosolic enzyme and expressed widely in the liver as part of the urea cycle, while it is also expressed in cells and tissues that lack a complete urea cycle, including lung. Inherited deficiency of this ARG1 causes argininemia, which is an autosomal recessive disorder characterized by hyperammonemia.

电泳(SDS-PAGE)

FOR RESEARCH USE ONLY