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VWF Protein (AA 49-230) (His tag)

Recombinant VWF protein expressed in Escherichia coli (E. coli).
Catalog No. ABIN7505493

Quick Overview for VWF Protein (AA 49-230) (His tag) (ABIN7505493)

Target

See all VWF Proteins
VWF (Von Willebrand Factor (VWF))

Protein Type

Recombinant

Origin

  • 10
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Rat

Source

  • 11
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
Escherichia coli (E. coli)

Purity

> 95 % as determined by reducing SDS-PAGE.
  • Protein Characteristics

    AA 49-230

    Purification tag / Conjugate

    This VWF protein is labelled with His tag.

    Sequence

    Lys 49-Asn 230

    Characteristics

    A DNA sequence encoding the Rat VWF protein (Q62935) (Lys 49-Asn 230) was expressed with a N-His tag.
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    Lyophilized from sterile PBS, pH 7.4.
    Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween80 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

    VWF (Von Willebrand Factor (VWF))

    Alternative Name

    VWF

    Background

    Abbreviation: VWF

    Target Synonym: F8VWF,Von Willebrand Factor,VWD,vWF,VWF

    Background: Von Willebrand Factor (VWF) is a multimeric glycoprotein involved in hemostasis in blood, binds receptors on the surface of platelets and in connective tissue, thereby mediating the adhesion of platelets to sites of vascular injury. From studies it appears that VWF protein uncoils under these circumstances, decelerating passing platelets. VWF protein is deficient or defective in von Willebrand disease (VWD) and is involved in a large number of other diseases, including thrombosis, thrombotic thrombocytopenic purpura, Stroke, Heyde's syndrome, possibly hemolytic-uremic syndrome and so on.

    Molecular Weight

    Calculated MW: 19.91 kDa

    Observed MW: 25 kDa

    UniProt

    Q62935
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