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          • Primary Antibodies ›
          • ATP7B Antibodies

          Invitrogen

          ATP7B Polyclonal Antibody, DyLight™ 488

          View all (29) ATP7B antibodies

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          Cite ATP7B Polyclonal Antibody, DyLight™ 488

          ATP7B Polyclonal Antibody, DyLight™ 488

          Product Details

          PA5-22769

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:1,000
          -

          Immunocytochemistry (ICC/IF)

          1:10-1:2,000
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          A synthetic peptide made to an internal sequence near the C-terminus of human ATP7b.
          View immunogen

          Conjugate

          DyLight™ 488 DyLight™ 488 DyLight™ 488

          Excitation/Emission Max

          492/519 nm View spectra spectra

          Form

          Liquid

          Concentration

          0.93 mg/mL

          Purification

          Antigen affinity chromatography

          Storage buffer

          50mM sodium borate

          Contains

          0.05% sodium azide

          Storage conditions

          4°C, store in dark

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          RRID

          AB_11152966

          Product Specific Information

          This antibody does not react with mouse samples.

          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-transporting ATPase 2; PINA gene, promoter; pineal night-specific ATPase; RP11-327P2.1; RP11-327P2.3; toxic milk; Wilson disease-associated protein; Wilson disease-associated protein homolog; Wilson protein

          View more View less

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

          View more View less

          UniProt ID: (Human) Q5T7X7, (Mouse) Q64446

          View more View less

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

          View more View less

          Function(s)
          copper-exporting ATPase activity copper ion binding protein binding ATP binding zinc ion binding copper-transporting ATPase activity copper ion transmembrane transporter activity cation-transporting ATPase activity nucleotide binding hydrolase activity metal ion binding primary active transporter
          Process(es)
          copper ion transport cellular copper ion homeostasis cellular zinc ion homeostasis lactation circadian rhythm response to zinc ion copper ion import intracellular copper ion transport ion transmembrane transport response to copper ion sequestering of calcium ion response to cAMP copper ion export metabolic process metal ion transport copper ion transmembrane transport cation transmembrane transport transport ion transport cation transport
          It has to be done as per old AB suggested Products section.
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          Performance Guarantee

          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

          Learn more
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          Get expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.

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