ATP7B Polyclonal Antibody

Background:
ATPase copper transporting beta(ATP7B) Homo sapiens 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, Jul 2008],

Alternative Names:
ATP7B, PWD, WC1, WND, Copper-transporting ATPase 2, Copper pump 2, Wilson disease-associated protein

Immunogen: The antiserum was produced against synthesized peptide derived from human ATP7B. AA range:161-210

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

GeneID: ATP7B

Storage: -20°C/1 year

NOTE: For Research Use Only