ATP7B Mouse anti-Human, Clone: 3A12, Invitrogen
Mouse Monoclonal Antibody
Manufacturer: Invitrogen MA518468
Peptide Sequence: QLKCYKKPDL ERYEAQAHGH MKPLTASQVS VHIGMDDRWR DSPRATPWDQ VSYVSQVSLS SLTSDKPSRH SAAADDDGDK WSLLLNGRDE EQYIThis 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).
|PBS with no preservative; pH 7.4|
|RP11-327P2.1, PWD, WC1, WD, WND, ATPase, Cu(2+)- transporting, beta polypeptide, Wilson disease-associated protein, copper pump 2, copper-transporting ATPase 2|
|-20° C, Avoid Freeze/Thaw Cycles|
|ELISA, Western Blot|
|ATP7B (NP_000044, 1372 a.a. ∽ 1465 a.a) partial recombit protein with GST tag. MW of the GST tag alone is 26 KDa.|
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