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Last updated: 2022/11/27

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ARG1 (Human) Recombinant Protein BioActive

  • Catalog # : P6839
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  • Specification
  • Product Description:
  • Human Arginase 1/ARG1 protein (NP_000036, 1 a.a.-322 a.a.) full length recombinant protein with His tag expressed in Escherichia coli.
  • Host:
  • Escherichia coli
  • Theoretical MW (kDa):
  • 35.8
  • Form:
  • Liquid
  • Preparation Method:
  • Escherichia coli expression system
  • Purity:
  • > 85% by SDS-PAGE
  • Activity:
  • Specific activity is > 150,000 pmol/min/ug, and is defined as the amount of enzyme that hydrolyze 1.0 pmole of arginine to urea per minute at pH 10.5 at 37°C.
  • Quality Control Testing:
  • SDS-PAGE under reducing condition and visualized by coomassie blue stain.

    QC Testing of P6839
    SDS-PAGE under reducing condition and visualized by coomassie blue stain.
  • Recommend Usage:
  • SDS-PAGE
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In 20 mM Tris-HCl, 100 mM NaCl, pH 8.0 (20% glycerol, 2 mM DTT)
  • Storage Instruction:
  • Store at -20°C. For long term storage store at -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Applications
  • SDS-PAGE
  • Application Image
  • SDS-PAGE
  • Gene Information
  • Entrez GeneID:
  • 383
  • Gene Name:
  • ARG1
  • Gene Alias:
  • -
  • Gene Description:
  • arginase, liver
  • Gene Summary:
  • 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. [provided by RefSeq
  • Other Designations:
  • A-I,OTTHUMP00000017209,arginase, type I
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