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Desmin Protein (DES) (His tag)

This Recombinant Desmin protein is produced in Escherichia coli (E. coli).
Catalog No. ABIN7668649

Quick Overview for Desmin Protein (DES) (His tag) (ABIN7668649)

Target

See all Desmin (DES) Proteins
Desmin (DES)

Protein Type

Recombinant

Biological Activity

Inactive

Origin

  • 10
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Source

  • 10
  • 7
  • 2
  • 2
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  • 1
Escherichia coli (E. coli)

Purity

> 95 %
  • Purification tag / Conjugate

    This Desmin protein is labelled with His tag.

    Purpose

    Recombinant Human DES protein (His tag)

    Sequence

    Ser 2-Leu 470

    Purification

    > 95 % as determined by reducing SDS-PAGE.

    Sterility

    0.2 μm filtered

    Endotoxin Level

    < 10 EU/mg of the protein as determined by the LAL method.
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis.

    Buffer

    Lyophilized from sterile PBS, 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

    Desmin (DES)

    Alternative Name

    DES

    Background

    Desmin is a cytoplasmic protein and belongs to the intermediate filament family. interacts with DST and MTM1. Desmin is only expressed in vertebrates, however homologous proteins are found in many organisms. Desmin is the main intermediate filament in mature skeletal, cardiac and smooth-muscle cells. DES founctions as homopolymers to form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. .Defects in DES are cause of the myopathy myofibrillar type 1, cardiomyopathy dilated type 1I, and neurogenic scapuloperoneal syndrome Kaeser type.,DES,Desmin,desmin

    Molecular Weight

    calculated_mw: 51.5 kDa

    observed_mw: 58 kDa

    UniProt

    P17661
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