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VWF Protein (DYKDDDDK Tag)

VWF Origine: Humain Hôte: Insect cells (Sf9) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735406
  • Antigène Voir toutes VWF Protéines
    VWF (Von Willebrand Factor (VWF))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    Humain
    Source
    • 12
    • 2
    • 1
    • 1
    • 1
    Insect cells (Sf9)
    Purification/Conjugué
    Cette VWF protéine est marqué à la DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human von Willebrand factor (VWF) (C-term DDK tag) protein expressed in sf9 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product VWF Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    50 mM Tris-HCl, pH 8.0, 100 mM glycine, 10 % glycerol. Store at -80C. Avoid repeated freeze-thaw cycles. Stable for at least 3 months from receipt of products under proper storage and handling conditions.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    VWF (Von Willebrand Factor (VWF))
    Abstract
    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
    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.
    Poids moléculaire
    67 kDa
    NCBI Accession
    NP_000543
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