anti- ATP7B antibody
Immunogen affinity purified
≥95% as determined by SDS-PAGE
PBS with 0.02% sodium azide and 50% glycerol pH 7.3,-20℃ for 24 months(Avoid repeated freeze / thaw cycles.)
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).
PWD, WC1, WD, WND
IHC: 1:50 – 1:200
Current product's manual: Manual
Protocol may be updated. Please feel free to contact Finetest Team to acquire the latest version.