ATP7B polyclonal antibody

Catalog # PAB12477

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Size:100 uL
Price: USD $ 531.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Tissue lysate)
Application

Western Blot (Tissue lysate)

Western blot analysis of ATP7B in 20 ug of mouse brain membrane fraction using ATP7B polyclonal antibody (Cat # PAB12477).

  • Specification

    Product Description

    Rabbit polyclonal antibody raised against synthetic peptide of ATP7B.

    Immunogen

    A synthetic peptide corresponding to N-terminus of human ATP7B.

    Host

    Rabbit

    Reactivity

    Human, Mouse

    Specificity

    This antibody is specific to ATP7b.

    Form

    Liquid

    Recommend Usage

    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Tris-citrate/phosphate buffer, pH 7.0-8.0 (0.09% sodium azide)

    Storage Instruction

    Store at 4°C. Do not freeze.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot (Tissue lysate)

    Western blot analysis of ATP7B in 20 ug of mouse brain membrane fraction using ATP7B polyclonal antibody (Cat # PAB12477).

    Immunohistochemistry

  • Gene Info — ATP7B

    Entrez GeneID

    540

    Protein Accession#

    P35670

    Gene Name

    ATP7B

    Gene Alias

    PWD, WC1, WD, WND

    Gene Description

    ATPase, Cu++ transporting, beta polypeptide

    Omim ID

    277900 606882

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    ATPase, Cu(2+)- transporting, beta polypeptide|OTTHUMP00000040880|Wilson disease-associated protein|copper pump 2|copper-transporting ATPase 2

  • Interactome
  • Disease
  • Publication Reference
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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