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重组人Arginase-1/ARG1Protein(C-6His)

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产品名称: 重组人Arginase-1/ARG1Protein(C-6His)
产品型号: PN100101-50ug
产品展商: PERFEMIKER
产品价格: 3520.00 元
会员价格: 0.00 元
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简单介绍

重组人Arginase-1/ARG1Protein(C-6His) 货号:PN100101 规格:50ug; 标签:C-6His; 来源:Human; 表达宿主:E.coli


重组人Arginase-1/ARG1Protein(C-6His)  的详细介绍

名称:重组人Arginase-1/ARG1Protein(C-6His);


产品说明(Description)
Recombinant Human Arginase-1 is produced by our E.coli 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,150mM NaCl,20% Glycerol,1mM DTT, pH 7.4.

质量控制(Quality Control) 
Purity: Greater than 95% 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. Inherited deficiency of this ARG1 causes argininemia, which is an autosomal recessive disorder characterized by hyperammonemia.

电泳(SDS-PAGE)

FOR RESEARCH USE ONLY