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          • Primary Antibodies ›
          • ATP7B Antibodies

          Antibodies Inc

          Copper ATPase 2 (Wilson's Disease Protein) Monoclonal Antibody (L62/29), FL594

          View all (30) ATP7B antibodies

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          Cite Copper ATPase 2 (Wilson's Disease Protein) Monoclonal Antibody (L62/29), FL594

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          Copper ATPase 2 (Wilson's Disease Protein) Monoclonal Antibody (L62/29), FL594

          Product Details

          75-143-FL594

          Applications
          Tested Dilution
          Publications

          Immunohistochemistry (Frozen) (IHC (F))

          Assay-dependent
          -

          Immunocytochemistry (ICC/IF)

          Assay-dependent
          -

          ELISA (ELISA)

          Assay-dependent
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Mouse / IgG1

          Class

          Monoclonal

          Type

          Antibody

          Clone

          L62/29

          Immunogen

          Synthetic peptide amino acids 3-21 (cytoplasmic N- terminus) of human Copper-transporting ATPase 2 (accession number P35670).
          View immunogen

          Conjugate

          FL594 FL594 FL594
          • Unconjugated
          • FL490
          • FL550
          • FL650
          • Request custom conjugation

          Excitation/Emission Max

          594/615 nm

          Form

          Liquid

          Concentration

          0.5 mg/mL

          Purification

          Protein A

          Storage buffer

          PBS

          Contains

          0.09% sodium azide

          Storage conditions

          Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

          Shipping conditions

          Ambient (domestic); Dry ice (international)

          Product Specific Information

          For maximum recovery of product, centrifuge the vial prior to removing the cap.

          Target Information

          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).

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          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 transport protein; mutant protein; Copper-transporting ATPase 2; copper-transporting protein ATP7B; ORF; PINA gene, promoter; pineal night-specific ATPase; putative; RP11-327P2.1; RP11-327P2.3; toxic milk; unnamed protein product; Wilson disease-associated protein; Wilson disease-associated protein homolog; Wilson protein

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          Gene Aliases: Atp7a; ATP7B; Hts; PINA; PWD; tx; WC1; WD; WND

          View more View less

          UniProt ID: (Human) P35670, (Mouse) Q64446

          View more View less

          Entrez Gene ID: (Human) 540, (Rat) 24218, (Mouse) 11979

          View more View less

          Function(s)
          nucleotide binding copper ion transmembrane transporter activity copper ion binding protein binding ATP binding ATPase activity cation-transporting ATPase activity copper-transporting ATPase activity metal ion binding P-type monovalent copper transporter activity copper-exporting ATPase activity zinc ion binding hydrolase activity primary active transporter
          Process(es)
          ion transport cation transport copper ion transport cellular copper ion homeostasis cellular zinc ion homeostasis lactation copper ion import ion transmembrane transport response to copper ion sequestering of calcium ion protein maturation establishment of localization in cell copper ion export viral translational frameshifting drug transmembrane export circadian rhythm metabolic process response to zinc ion intracellular copper ion transport metal ion transport copper ion transmembrane transport response to cAMP cation transmembrane transport transport
          It has to be done as per old AB suggested Products section.

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