Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

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

TPM1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5513939

Aperçu rapide pour Tropomyosin 1 (Alpha) (TPM1) (N-Term) Peptide (ABIN5513939)

Antigène

Tropomyosin (TPM1) (Tropomyosin 1 (Alpha) (TPM1))

Origine

Humain

Source

  • 4
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Séquence

    DAEADVASLN RRIQLVEEEL DRAQERLATA LQKLEEAEKA ADESERGMKV

    Attributs du produit

    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.
  • 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

    Tropomyosin (TPM1) (Tropomyosin 1 (Alpha) (TPM1))

    Sujet

    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

    ID gène

    7168

    NCBI Accession

    XP_006720731

    UniProt

    P09493
Vous êtes ici:
Chat with us!