The synthetic peptide sequence is 1451-1465aa, DKWSLLLNGRDEEQYI
Add 0.2 mL of distilled water, will yield a concentration of 500 µg/mL.
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).
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: ATPase, Cu(2+)- transporting, beta polypeptide; ATPase, Cu++ transporting, beta polypeptide; ATPase, Cu++ transporting, beta polypeptide (same as Wilson disease); Copper pump 2; Copper-transporting ATPase 2; PINA gene, promoter; pineal night-specific ATPase; toxic milk; Wilson disease-associated protein; Wilson disease-associated protein homolog; Wilson protein; WND/140 kDa
Gene Aliases: Atp7a; ATP7B; Hts; PINA; PWD; tx; WC1; WD; WND