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VWF Protein (His tag)

VWF Origine: Humain Hôte: HEK-293 Cells Recombinant The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.
N° du produit ABIN7092835
  • Antigène Voir toutes VWF Protéines
    VWF (Von Willebrand Factor (VWF))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    Humain
    Source
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette VWF protéine est marqué à la His tag.
    Fonction
    Recombinant human VWF(23-763) protein with C-terminal 6xHis tag
    Specificité
    VWF (Als23-Arg763) 6xHis tag
    Attributs du produit
    Extracellular Domain Protein
    Purification
    affinity purification
    Pureté
    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 Protéine
  • 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.
    Stock
    -20 °C,-80 °C
    Stockage commentaire
    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.
    Date de péremption
    12 months
  • Antigène
    VWF (Von Willebrand Factor (VWF))
    Autre désignation
    VWF (VWF Produits)
    Synonymes
    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
    Sujet
    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]
    Poids moléculaire
    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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