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VWF Protein (His tag)

VWF Origin: Human Host: HEK-293 Cells Recombinant The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.
Catalog No. ABIN7092835
  • Target See all VWF Proteins
    VWF (Von Willebrand Factor (VWF))
    Protein Type
    Recombinant
    Origin
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    Human
    Source
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This VWF protein is labelled with His tag.
    Purpose
    Recombinant human VWF(23-763) protein with C-terminal 6xHis tag
    Specificity
    VWF (Als23-Arg763) 6xHis tag
    Characteristics
    Extracellular Domain Protein
    Purification
    affinity purification
    Purity
    The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.
    Top Product
    Discover our top product VWF Protein
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Reconstitute with deionized water
    Buffer
    Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.
    Storage
    -20 °C,-80 °C
    Storage Comment
    Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
    Expiry Date
    12 months
  • Target
    VWF (Von Willebrand Factor (VWF))
    Alternative Name
    VWF (VWF Products)
    Synonyms
    VWF Protein, si:ch1073-474e24.1 Protein, F8VWF Protein, VWD Protein, 6820430P06Rik Protein, AI551257 Protein, B130011O06Rik Protein, C630030D09 Protein, von Willebrand factor Protein, Von Willebrand factor Protein, VWF Protein, vwf Protein, Vwf Protein
    Background
    Synonymes: F8VWF,VWD
    Description: This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]
    Molecular Weight
    predicted molecular mass of 82.2 kDa after removal of the signal peptide. The apparent molecular mass of VWF(23-763)-His is 100-130 kDa due to glycosylation.
    UniProt
    P04275
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