ATP7B Full-Length MS Protein Standard


Product Description:

Name ATP7B Full-Length MS Protein Standard
Cat# CPFL323635
Protein NameATPase, Cu++ transporting, beta polypeptide
SymbolATP7B
SynonymsPWD; WC1; WD; WND
AccessionNM_000053
Cytogenetic13q14.3
Amino Acid Labeled[U- 13C6, 15N4]-L-Arg and [U- 13C6, 15N2]-L-Lys
Chemical Purity> 80% as determined by SDS-PAGE and Coomassie blue staining
Expression HostHuman HEK293 cells
Predicted MW157.1 kDa
Expression TrueORF CloneRC223635
DescriptionATP7B Full-Length MS Protein Standard (NP_000044), Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine, was produced in human 293 cells (HEK293) with fully chemically defined cell culture medium to obtain incorporation efficiency at Creative-Proteomics. 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).

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