Tissue expression
Cell line expression
Protein structure
ATP7B
ATPase copper transporting betaWND
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 is a monomer, and functions as a copper-transporting ATPase which exports 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 which is characterized by copper accumulation. [provided by RefSeq, Dec 2019]
Top validated antibodies |
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Novus Biologicals | NB100-360 | 14 references | Polyclonal |
WB
ICC
IP
IHC |
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GeneTex | GTX30639 | 2 references | Polyclonal |
WB
ICC
IP
IHC |
|
Invitrogen Antibodies | PA5-13429 | Polyclonal |
WB
ICC
IHC
FC
OA
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antibodies-online | ABIN151824 | 8 references | Polyclonal |
WB
ICC
IP
IHC |
|
Abgent | AP6504B | Polyclonal |
WB
ICC
IHC
FC |
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