Anti-Type I arginase antibody produced in rabbit
- Product NameAnti-Type I arginase antibody produced in rabbit
- CAS
- CBNumberCB22878270
- MW0
- MOL FileMol file
Chemical Properties
storage temp. | -20°C |
form | buffered aqueous glycerol solution |
Anti-Type I arginase antibody produced in rabbit Price
Product number | Packaging | Price | Product description | Buy |
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Sigma-Aldrich AV45673 | 100μL | $381 | Anti-ARG1 (AB2) antibody produced in rabbit IgG fraction of antiserum |
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Sigma-Aldrich HPA003595 | 25μL | $282 | Anti-ARG1 antibody produced in rabbit Prestige Antibodies? Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution |
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Sigma-Aldrich HPA003595 | 100μL | $547 | Anti-ARG1 antibody produced in rabbit Prestige Antibodies? Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution |
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Sigma-Aldrich AMAB90545 | 25μL | $186 | Monoclonal Anti-ARG1 antibody produced in mouse Prestige Antibodies? Powered by Atlas Antibodies, clone CL0186, purified immunoglobulin, buffered aqueous glycerol solution |
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Sigma-Aldrich AMAB90545 | 100μL | $507 | Monoclonal Anti-ARG1 antibody produced in mouse Prestige Antibodies? Powered by Atlas Antibodies, clone CL0186, purified immunoglobulin, buffered aqueous glycerol solution |
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Anti-Type I arginase antibody produced in rabbit Chemical Properties,Usage,Production
Uses
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.Western Blotting (1 paper)
General Description
ARG1 (arginase 1) is an enzyme responsible for the processing of the essential amino acid arginine, to produce urea and L-ornithine. This enzyme is expressed in the presence of Th2 (T-helper) cytokines such as, interleukin (IL-4), IL-13 and TGFβ (tumor growth factor).Biochem/physiol Actions
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 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.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.Preparation Products And Raw materials
Anti-Type I arginase antibody produced in rabbit Suppliers
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