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Invitrogen™ ATP7B Recombinant Rabbit Monoclonal Antibody (36D12)

Rabbit Recombinant Monoclonal Antibody

Supplier:  Invitrogen™ MA550124

Catalog No. FEMA550124


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Description

Description

ATP7B Recombinant Monoclonal Antibody for ICC/IF, IHC (P), Flow, ELISA

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).
TRUSTED_SUSTAINABILITY
Specifications

Specifications

ATP7B
Recombinant Monoclonal
0.46 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
P35670
Atp7b
A synthesized peptide derived from Human ATP7B.
100 μL
Primary
Human
Antibody
IgG
ELISA, Flow Cytometry, Immunohistochemistry (Paraffin), Immunocytochemistry
36D12
Unconjugated
Atp7b
Atp7a; ATP7B; ATPase copper transporting beta; 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; Hts; PINA; PINA gene, promoter; pineal night-specific ATPase; PWD; RP11-327P2.1; RP11-327P2.3; toxic milk; tx; WC1; WD; Wilson disease-associated protein; wilson disease-associated protein homolog; Wilson protein; Wnd; WND/140 kDa
Rabbit
Affinity chromatography
RUO
540
-20°C or -80°C if preferred
Liquid
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