This is an aptamer development services to screening aptamers binds to the ATP7A with an affinity of 1nM~1μM.
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| Target Category | Protein |
| Target | ATP7A |
| Alternative Names | ATPase Copper Transporting Alpha; Copper-Transporting ATPase 1; Copper Pump 1; ATPase, Cu++ Transporting, Alpha Polypeptide; Menkes Disease-Associated Protein; MNK; Cu++-Transporting P-Type ATPase; Menkes Syndrome; DSMAX; SMAX3; ATP7A; MC1; MK |
| Gene ID | 538 |
| UniProt ID | Q04656 |
| Target Overview | 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. |
| Chemical Modification | N/A |
| Type | DNA |
| Length | 20-80 nt |
| Affinity (Kd) | 1nM~1μM |
| Binding Conditions/Buffer | PBS; buffer system with Serum; other |