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C261

Recombinant Human Tropomyosin α-1 chain/TPM1

10ug

1200

1080

现货

国产

C261

Recombinant Human Tropomyosin α-1 chain/TPM1

50ug

3520

3168

现货

国产

C261

Recombinant Human Tropomyosin α-1 chain/TPM1

500ug

12320

11088

现货

国产

C261

Recombinant Human Tropomyosin α-1 chain/TPM1

1mg

17600

15840

现货

国产

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  • Catalog# C261
    Source E.coli
    Description Recombinant Human Tropomyosin α-1 Chain/TPM1 is produced by our E. coli expression system. The target protein is expressed with sequence (Met1-Met284) of Human TPM1 fused with a His tag at the N-terminus.
    Names Tropomyosin Alpha-1 Chain, Alpha-Tropomyosin, Tropomyosin-1, TPM1, C15orf13, TMSA
    Accession # P09493
    Formulation Supplied as a 0.2 μm filtered solution of 20mM Tris, 1mM DTT, 100mM NaCl, 20% Glycerol, pH 8.0
    Shipping The product is shipped on dry ice/ice packs.
    Storage Store at < -20°C, stable for 6 months after receipt.
    Please minimize freeze-thaw cycles.
    Purity Greater than 95% as determined by reducing SDS-PAGE.
    Endotoxin Less than 0.1 ng/μg (1 IEU/μg).
    Amino Acid Sequence
    MGSSHHHHHHSSGLVPRGSHMDAIKKKMQMLKLDKENALDRAEQAEADKKAAEDRSKQLEDELVS LQKKLKGTEDELDKYSEALKDAQEKLELAEKKATDAEADVASLNRRIQLVEEELDRAQERLATAL QKLEEAEKAADESERGMKVIESRAQKDEEKMEIQEIQLKEAKHIAEDADRKYEEVARKLVIIESD LERAEERAELSEGQVRQLEEQLRIMDQTLKALMAAEDKYSQKEDRYEEEIKVLSDKLKEAETRAE FAERSVTKLEKSIDDLEDELYAQKLKYKAISEELDHALNDMTSM
    Background Tropomyosin α-1 Chain (TPM1) is a member of the Tropomyosin family of highly conserved and widely distributed Actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. TPM1 binds to Actin filaments in both muscle and non-muscle cells. It is one type of α-helical chain that forms the predominant Tropomyosin of striated muscle. TPM1 plays a central role in association with the Troponin complex and the Calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with Caldesmon. In non-muscle cells, it is implicated in stabilizing the cytoskeleton Actin filaments. Defects in TPM1 are associated with type 3 Familial Hypertrophic Cardiomyopathy.