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Tropomyosin 1 (Alpha) (TPM1) (N-Term) Peptid

TPM1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN5513939
  • Target Alle Tropomyosin (TPM1) Produkte
    Tropomyosin (TPM1) (Tropomyosin 1 (Alpha) (TPM1))
    Protein Region
    N-Term
    Spezies
    Human
    Quelle
    • 4
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    DAEADVASLN RRIQLVEEEL DRAQERLATA LQKLEEAEKA ADESERGMKV
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-TPM1 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.
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    Tropomyosin (TPM1) (Tropomyosin 1 (Alpha) (TPM1))
    Hintergrund
    This gene is a member of the tropomyosin family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosin is composed of two alpha-helical chains arranged as a coiled-coil. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments. The encoded protein is one type of alpha helical chain that forms the predominant tropomyosin of striated muscle, where it also functions in association with the troponin complex to regulate the calcium-dependent interaction of actin and myosin during muscle contraction. In smooth muscle and non-muscle cells, alternatively spliced transcript variants encoding a range of isoforms have been described. Mutations in this gene are associated with type 3 familial hypertrophic cardiomyopathy.

    Alias Symbols: TPM1,C15orf13,TMSA,

    Protein Size: 284
    Gen-ID
    7168
    NCBI Accession
    XP_006720731
    UniProt
    P09493
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