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ARG1 polyclonal antibody

  • Catalog # : PAB24634
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of ARG1.
  • Immunogen:
  • A synthetic peptide corresponding to N-terminus of human ARG1.
  • Host:
  • Rabbit
  • Theoretical MW (kDa):
  • 35
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Immunogen affinity purification
  • Isotype:
  • IgG
  • Recommend Usage:
  • Western Blot (1:100)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:100)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.6 (1% BSA, 0.09% sodium azide)
  • Storage Instruction:
  • Store at 4°C. Do not freeze.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • Western blot analysis of MOLT 4 cell lysate with ARG1 polyclonal antibody (Cat # PAB24634).
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) of human hepatocellular carcinoma tissue with ARG1 polyclonal antibody (Cat # PAB24634).
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • 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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