Tropomyosin α rabbit pAb

CAT:
855-ES3644-01
Size:
50 µL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Tropomyosin α rabbit pAb - image 1

Tropomyosin α rabbit pAb

  • Background :

    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. [provided by
  • Description :

    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. [provided by
  • Product Name Alternative :

    TPM1; C15orf13; TMSA; Tropomyosin alpha-1 chain; Alpha-tropomyosin; Tropomyosin-1
  • UniProt :

    P09493
  • Swiss Prot :

    P09493
  • Reactivity :

    Human; Mouse; Rat
  • Immunogen :

    The antiserum was produced against synthesized peptide derived from human Tropomyosin alpha. AA range:40-89
  • Target :

    Tropomyosin α
  • Clonality :

    Polyclonal
  • Source :

    Rabbit
  • Applications :

    WB; ELISA
  • Concentration :

    1 mg/ml
  • Dilution :

    Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
  • Buffer :

    -20°C/1 year
  • Molecular Weight :

    35kD
  • Storage Conditions :

    -20°C/1 year
  • Observed Molecular Weight :

    35kD
  • Fragment :

    IgG
  • Subcellular Location :

    Cytoplasm, cytoskeleton . Associates with F-actin stress fibers. .
  • Other Product Names :

    TPM1; C15orf13; TMSA; Tropomyosin alpha-1 chain; Alpha-tropomyosin; Tropomyosin-1
  • Gene ID (Human) :

    7168

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