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Last updated: 2016/12/4
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GJA1 polyclonal antibody

  • Catalog # : PAB14139
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of GJA1.
  • Immunogen:
  • A synthetic peptide corresponding to human GJA1.
  • Sequence:
  • C-QPFDFPDDNQNSKK
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 43
  • Reactivity:
  • Rat
  • Specificity:
  • Approx 40 KDa band observed in rat brain lysates (calculated MW of 43.0 KDa according to human NP_000156.1 and to Rat NP_036699.1).
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Recommend Usage:
  • ELISA (1:64000)
    Western Blot (0.3-1 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)
  • GJA1 polyclonal antibody (Cat # PAB14139) (0.3 ug/mL) staining of rat brain 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:
  • 2697
  • Gene Name:
  • GJA1
  • Gene Alias:
  • CX43,DFNB38,GJAL,ODDD
  • Gene Description:
  • gap junction protein, alpha 1, 43kDa
  • Gene Summary:
  • This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia and heart malformations. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000017111,connexin 43,gap junction 43 kDa heart protein,gap junction protein, alpha-like
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