CTSK monoclonal antibody, clone CTSK/2791

Catalog # MAB21166

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Price

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Quantity

Size:100 ug
Price: USD $ 428.00
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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
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human liver with CTSK monoclonal antibody, clone CTSK/2791 (Cat # MAB21166).

  • Specification

    Product Description

    Mouse monoclonal antibody raised against partial recombinant human CTSK.

    Immunogen

    Recombinant protein corresponding to amino acids 163-274 of human CTSK.

    Host

    Mouse

    Theoretical MW (kDa)

    39

    Reactivity

    Human

    Form

    Liquid

    Purification

    Protein A/G purification

    Isotype

    IgG, kappa

    Recommend Usage

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1-2 ug/mL)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 10 mM PBS.

    Storage Instruction

    Store at -20 to -80°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human liver with CTSK monoclonal antibody, clone CTSK/2791 (Cat # MAB21166).
  • Gene Info — CTSK

    Entrez GeneID

    1513

    Protein Accession#

    P43235

    Gene Name

    CTSK

    Gene Alias

    CTS02, CTSO, CTSO1, CTSO2, MGC23107, PKND, PYCD

    Gene Description

    cathepsin K

    Omim ID

    265800 601105

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. This gene may be subject to RNA editing. [provided by RefSeq

    Other Designations

    OTTHUMP00000032938|cathepsin O1|cathepsin O2|cathepsin X

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