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Last updated: 2016/11/27
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ARG1 polyclonal antibody

  • Catalog # : PAB15607
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised aganist synthetic peptide of ARG1.
  • Immunogen:
  • A synthetic peptide corresponding to human ARG1.
  • Sequence:
  • CFGLAREGNHKPID
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 34.7
  • Reactivity:
  • Human
  • Specificity:
  • Approximately 37 KDa band observed in human liver lysates (calculated MW of 34.7 KDa according to NP_000036.2). The observed molecular weight corresponds to earlier findings with different antibodies from other commercial sources.
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Recommend Usage:
  • ELISA (1:64000)
    Western Blot (0.01-0.03 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • ARG1 polyclonal antibody (Cat # PAB15607) (0.01 ug/mL) staining of human liver lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • 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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