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Last updated: 2017/1/15
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ATP7A polyclonal antibody

  • Catalog # : PAB11502
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of ATP7A.
  • Immunogen:
  • A synthetic peptide corresponding to human ATP7A.
  • Sequence:
  • C-HKNNWNIEDNNIKN
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 163
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:8000)
    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
  • ELISA
  • Application Image
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 538
  • Gene Name:
  • ATP7A
  • Gene Alias:
  • FLJ17790,MK,MNK
  • Gene Description:
  • ATPase, Cu++ transporting, alpha polypeptide
  • Gene Summary:
  • This gene encodes a transmembrane protein that functions in copper transport across membranes. The protein localizes to the trans-Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. The protein relocalizes to the plasma membrane under conditions of elevated extracellular copper and functions in the efflux of copper from cells. Mutations in this gene result in Menkes disease, X-linked cutis laxa, and occipital horn syndrome. [provided by RefSeq
  • Other Designations:
  • Cu++-transporting P-type ATPase,Menkes disease-associated protein,Menkes syndrome,OTTHUMP00000023593,OTTHUMP00000062077,copper pump 1,copper-transporting ATPase 1
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