| Product Name | ATP7A Antibody |
|---|---|
| Description | Rabbit polyclonal antibody to ATP7A |
| Synonyms | ATP 7A antibody; ATP7A antibody; ATP7A_HUMAN antibody; ATPase copper transporting alpha polypeptide antibody; ATPase Cu++ transporting alpha polypeptide (Menkes syndrome) antibody; ATPase Cu++ transporting alpha polypeptide antibody; Copper pump 1 antibody; Copper transporting ATPase 1 antibody; Copper-transporting ATPase 1 antibody; Cu++ transporting P type ATPase antibody; DSMAX antibody; FLJ17790 antibody; MC 1 antibody; MC1 antibody; Menkes disease associated protein antibody; Menkes disease-associated protein antibody; Menkes syndrome antibody; MK antibody; MNK antibody; OHS antibody; OTTHUMP00000062077 antibody; SMAX3 antibody |
| Host | Rabbit |
| Clonality | Polyclonal |
| Conjugate | Unconjugated |
| Immunogen | Synthetic peptide of human ATP7A |
| Isotype | IgG |
| Target | ATP7A |
| Reactivity | Human, Mouse, Rat |
| Applications | ELISA, IHC, WB |
| Form | Liquid |
| Diluent Buffer | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Uniprot | Q04656 |
| Storage | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
| 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. |
| Supplier | Cusabio |
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