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Adenomatous Polyposis Coli (APC) (Middle Region) Peptide

APC Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5512735
  • Antigène Tous les produits APC
    APC (Adenomatous Polyposis Coli (APC))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    SETFDNIDNL SPKASHRSKQ RHKQSLYGDY VFDTNRHDDN RSDNFNTGNM
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-APC Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    APC (Adenomatous Polyposis Coli (APC))
    Synonymes
    dp2 Peptide, dp3 Peptide, fap Peptide, fpc Peptide, xapc Peptide, dp2.5 Peptide, AI047805 Peptide, AU020952 Peptide, AW124434 Peptide, CC1 Peptide, Min Peptide, mAPC Peptide, BTPS2 Peptide, DP2 Peptide, DP2.5 Peptide, DP3 Peptide, GS Peptide, PPP1R46 Peptide, RATAPC Peptide, APC1 Peptide, APC, WNT signaling pathway regulator Peptide, adenomatous polyposis coli Peptide, adenomatous polyposis coli protein, putative Peptide, adenomatosis polyposis coli Peptide, adenomatous polyposis coli L homeolog Peptide, APC Peptide, apc Peptide, Smp_139190 Peptide, Apc Peptide, apc.L Peptide
    Sujet
    This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product.

    Alias Symbols: GS, DP2, DP3, BTPS2, DP2.5, PPP1R46

    Protein Size: 1304
    ID gène
    324
    NCBI Accession
    NM_000038, NP_000029
    UniProt
    E9PFT7
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