ATP7A Antibody


Western Blot: ATP7A Antibody [NBP1-51275] - Lane1: Hela whole cell lysate. Lane2: NIH-3T3 whole cell lysate. Lane3: Rat brain tissue lysate.
Immunohistochemistry-Paraffin: ATP7A Antibody [NBP1-51275] - Human brain tissue.

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ATP7A Antibody Summary

Synthetic peptide, corresponding to amino acids 620-670 of Human ATP7A.
ATP7A (H640) pAb detects endogenous levels of ATP7A protein.
Immunogen affinity purified
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  • Western Blot 1:500-1:1000
  • Immunohistochemistry 1:50-1:200
  • Immunohistochemistry-Paraffin 1:50-1:200
Application Notes
Immunohistochemistry (IHC) analyzes of ATP7A (H640) pAb in paraffin-embedded human brain tissue.
Theoretical MW
163 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Packaging, Storage & Formulations

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
PBS (pH 7.2)
0.05% Sodium Azide
1.0 mg/ml
Immunogen affinity purified

Alternate Names for ATP7A Antibody

  • ATPase, Cu++ transporting, alpha polypeptide
  • Copper pump 1
  • copper-transporting ATPase 1
  • Cu++-transporting P-type ATPase
  • EC 3.6.3
  • EC
  • MC1
  • Menkes disease-associated protein
  • Menkes syndrome
  • MK
  • MNKFLJ17790
  • OHS
  • SMAX3


Copper-transporting ATPase 1 is an integral membrane protein cycling constitutively between the trans-golgi network and the plasma membrane. It may supply copper to copper-requiring proteins within the secretory pathway, when localized in the trans-golgi network. Under conditions of elevated extracellular copper, it relocalized to the plasma membrane where it functions in the efflux of copper from cells.Defects in ATP7A are the cause of Menkes syndrome ; also known as kinky hair disease, an X-linked recessive disorder.


This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Gene Symbol ATP7A