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TPM3 Protéine

Protéine Recombinant TPM3 exprimée dans Escherichia coli (E. coli).
N° du produit ABIN7319117
287,60 €
Plus frais de livraison 40,00 € et TVA
Destination: France
Envoi sous 9 à 13 jours ouvrables

Aperçu rapide pour TPM3 Protéine (ABIN7319117)

Antigène

Voir toutes TPM3 Protéines
TPM3 (Tropomyosin 3 (TPM3))

Type de proteíne

Recombinant

Origine

  • 15
  • 1
  • 1
  • 1
  • 1
Humain

Source

  • 11
  • 4
  • 2
  • 1
  • 1
Escherichia coli (E. coli)

Pureté

> 90 % as determined by reducing SDS-PAGE.
  • Fonction

    Recombinant Human Tropomyosin α-3 Chain/TPM3 Protein

    Séquence

    Met 1-Met248

    Attributs du produit

    Recombinant Human Tropomyosin alpha-3 Chain is produced by our E.coli expression system and the target gene encoding Met1-Met248 is expressed.

    Stérilité

    0.2 μm filtered

    niveau d'endotoxine

    < 1.0 EU per μg of the protein as determined by the LAL method.

    Biological Activity Comment

    Not validated for activity
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    Lyophilized from a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.4.
    Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween 80 are added as protectants before lyophilization.

    Stock

    4 °C,-20 °C,-80 °C

    Stockage commentaire

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.

    Date de péremption

    12 months
  • Antigène

    TPM3 (Tropomyosin 3 (TPM3))

    Autre désignation

    Tropomyosin alpha-3 Chain/TPM3

    Sujet

    Gamma-Tropomyosin,TPM3,Tropomyosin Alpha-3 Chain,Tropomyosin-3,Tropomyosin-5,hTM5,Tropomyosin Alpha-3 Chain (TPM3) is a member of the Tropomyosin family. TPM3 exists as a heterodimer consisting of an alpha and a beta chain. TPM3 plays a central role in association with the Troponin complex and in the calcium dependent regulation of vertebrate striated muscle contraction. Defects in TPM3 are the cause of thyroid papillary carcinoma. Mutations in the TPM3 gene cause autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this locus are linked with cancer.

    Poids moléculaire

    Calculated MW: 29.0 kDa

    Observed MW: 32 kDa

    ID gène

    7170

    UniProt

    P06753
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