ATP7b antibody [S62-29]

Cannot supply to this region.

SKU:: GTX03698
Additional Names:: ATPase copper transporting beta , PWD , WC1 , WD , WND
Application:: IHC, WB, IF, ICC, IP
Concentration:: 1 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Protein G Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Mouse
Reactivities:: Human, Mouse, Rat
Buffer:: PBS, 50% Glycerol, 0.09% sodium azide.
Immunogen:: Synthetic peptide amino acids 3-21 (cytoplasmic N-terminus) of human Copper-transporting ATPase2
Clone:: S62-29
Uniprot:: P35670
Synonyms:: ATPase, Cu(2+)- transporting, beta polypeptide;ATPase, Cu++ transporting, beta polypeptide;copper pump 2;copper-transporting ATPase 2;copper-transporting protein ATP7B;PWD;WC1;WD;Wilson disease-associated protein;WND
Extra Details:: 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). [provided by RefSeq, Jul 2008]

Shipping Conditions:: Blue Ice