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TPM3 Protein

Recombinant TPM3 protein expressed in Escherichia coli (E. coli).
Catalog No. ABIN7319117
$307.73
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Quick Overview for TPM3 Protein (ABIN7319117)

Target

See all TPM3 Proteins
TPM3 (Tropomyosin 3 (TPM3))

Protein Type

Recombinant

Origin

  • 15
  • 1
  • 1
  • 1
  • 1
Human

Source

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

Purity

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

    Recombinant Human Tropomyosin α-3 Chain/TPM3 Protein

    Sequence

    Met 1-Met248

    Characteristics

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

    Sterility

    0.2 μm filtered

    Endotoxin Level

    < 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.

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    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.

    Expiry Date

    12 months
  • Target

    TPM3 (Tropomyosin 3 (TPM3))

    Alternative Name

    Tropomyosin alpha-3 Chain/TPM3

    Background

    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.

    Molecular Weight

    Calculated MW: 29.0 kDa

    Observed MW: 32 kDa

    Gene ID

    7170

    UniProt

    P06753
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