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Render Timestamp:
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6/12/2026, 10:43:26 AM UTC
Commit: a854f3e2d877b833e27badd637de63a8a4794b83
XML generation date: 2026-05-27 16:20:28.108
Product last modified at: 2026-05-28T07:00:59.849Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
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Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

Plakophilin 2 (8H6) Mouse Monoclonal Antibody #55133

Filter:
  • WB
  • IF

    Product Specifications

    REACTIVITY H Mk
    SENSITIVITY Endogenous
    MW (kDa) 97
    Source/Isotype Mouse IgG1 kappa
    Application Key:
    • WB-Western Blotting 
    • IF-Immunofluorescence 
    Species Cross-Reactivity Key:
    • H-Human 
    • Mk-Monkey 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000
    Simple Western™ 1:10 - 1:50
    Immunofluorescence (Immunocytochemistry) 1:200

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    Plakophilin 2 (8H6) Mouse Monoclonal Antibody recognizes endogenous levels of total plakophilin 2 protein. Based on the sequence of the protein antigen, this antibody is expected to detect all isoforms of plakophilin 2.

    Species Reactivity:

    Human, Monkey

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with recombinant protein specific to the amino terminus of human plakophilin 2 protein.

    Background

    Plakophilin 2 (PKP2), a member of the armadillo repeat protein family, is a key component of the desmosomal plaque and plays an essential role in intercellular adhesion. It contributes to the assembly and stabilization of desmosomal complexes by linking desmosomal cadherins to desmoplakin, thereby facilitating the anchorage of desmoplakin to intermediate filaments within the cytoskeleton (1,2).

    PKP2 is highly expressed in cardiac intercalated discs, where it is critical for maintaining the mechanical integrity of the myocardium (1,3). PKP2 mutations are associated with arrhythmogenic cardiomyopathy (ACM), a hereditary disorder characterized by defective desmosomes, which cause myocardium to be replaced with fibrofatty tissue, leading to arrhythmias and increased risk of sudden cardiac death (3).

    PKP2 plays a context-dependent role in cancer and may influence tumor progression by modulating cell–cell adhesion and signaling pathways, such as Wnt/β-Catenin and epidermal growth factor receptor (EGFR) (4,5). Studies have demonstrated PKP2 overexpression in lung adenocarcinoma and gastric cancer, whereas PKP2 downregulation in colorectal cancer has been associated with poor prognosis and metastasis (4-6).

    Alternate Names

    ARVD9; MGC177501; PKP2; plakophilin 2; Plakophilin-2

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