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ATP7B Rabbit anti-Human, Polyclonal Antibody, Abnova™
Descripción
This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD). [provided by RefSeq
Especificaciones
Especificaciones
| Antígeno | ATP7B |
| Aplicaciones | Immunocytochemistry, Western Blot |
| Clasificación | Polyclonal |
| Conjugado | Unconjugated |
| Descripción | Rabbit polyclonal antibody raised against synthetic peptide of ATP7B. |
| Dilución | Western Blot (1:1000) The optimal working dilution should be determined by the end user. |
| Formulación | In Tris-citrate/phosphate buffer, pH 7.0-8.0 (0.09% sodium azide) |
| génica | ATP7B |
| N.º de referencia del gen | P35670 |
| Alias de gen | PWD/WC1/WD/WND |
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For Research Use Only
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