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TPM3 Protein

Recombinant TPM3-Protein exprimiert in Escherichia coli (E. coli).
Produktnummer ABIN7319117
287,60 €
Zzgl. Versandkosten 20,00 € und MwSt
Lieferung nach: Deutschland
Lieferung in 9 bis 13 Werktagen

Kurzübersicht für TPM3 Protein (ABIN7319117)

Target

Alle TPM3 Proteine anzeigen
TPM3 (Tropomyosin 3 (TPM3))

Protein-Typ

Recombinant

Spezies

  • 15
  • 1
  • 1
  • 1
  • 1
Human

Quelle

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

Reinheit

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

    Recombinant Human Tropomyosin α-3 Chain/TPM3 Protein

    Sequenz

    Met 1-Met248

    Produktmerkmale

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

    Sterilität

    0.2 μm filtered

    Endotoxin-Niveau

    < 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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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • 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.

    Lagerung

    4 °C,-20 °C,-80 °C

    Informationen zur Lagerung

    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.

    Haltbarkeit

    12 months
  • Target

    TPM3 (Tropomyosin 3 (TPM3))

    Andere Bezeichnung

    Tropomyosin alpha-3 Chain/TPM3

    Hintergrund

    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.

    Molekulargewicht

    Calculated MW: 29.0 kDa

    Observed MW: 32 kDa

    Gen-ID

    7170

    UniProt

    P06753
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