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Invitrogen™ ATP7B Monoclonal Antibody (L62/29), FITC

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA545523

Catalog No. PIMA545523


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Description

Description

1 μg/mL of MA5-45523 was sufficient for detection of Copper-transporting ATPase2 in 20 μg of rat brain lysate by colorimetric immunoblot analysis using Goat IgG:HRP as the secondary antibody. Detects approximately 160kDa in rat brain membrane preparations. This antibody was formerly sold as clone S62-29.

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
Monoclonal
1 mg/mL
PBS, 9.1 mM sodium bicarbonate with 640.91 mM DMSO, 136.36 mM ethanolamine and no preservative; pH 7.4
P35670, Q64446, Q64535
Atp7b
Synthetic peptide amino acids 3-21 (cytoplasmic N-terminus) of human Copper-transporting ATPase2.
100 μg
Primary
Human, Mouse, Rat
Antibody
IgG1
Immunohistochemistry, Immunoprecipitation, Western Blot, Immunocytochemistry
L62/29
FITC
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
Mouse
Protein G
RUO
11979, 24218, 540
4°C, store in dark
Liquid
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