ATP7A Polyclonal Antibody

Background:
This gene encodes a transmembrane protein that functions in copper transport across membranes. This protein is localized to the trans Golgi network, where it is predicted to supply copper to copper-dependent enzymes in the secretory pathway. It relocalizes to the plasma membrane under conditions of elevated extracellular copper, and functions in the efflux of copper from cells. Mutations in this gene are associated with Menkes disease, X-linked distal spinal muscular atrophy, and occipital horn syndrome. Alternatively-spliced transcript variants have been observed.

Research Area: Cancer, Metabolism, Neuroscience, Signal Transduction

Synonyms:
ATP7A, DSMAX, MK, MNK, SMAX3

Immunogen: Recombinant fusion protein of human ATP7A (NP_000043.4).

Swissprot: Q04656
Gene ID: 538

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: "IHC 1:50-1:100"

Storage:
Store at -20°C. Avoid freeze / thaw cycles.