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VWF Protein (DYKDDDDK Tag)

VWF Spezies: Human Wirt: Insect cells (Sf9) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2735406
  • Target Alle VWF Proteine anzeigen
    VWF (Von Willebrand Factor (VWF))
    Protein-Typ
    Recombinant
    Spezies
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    Human
    Quelle
    • 12
    • 2
    • 1
    • 1
    • 1
    Insect cells (Sf9)
    Aufreinigungstag / Konjugat
    Dieses VWF Protein ist gelabelt mit DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human von Willebrand factor (VWF) (C-term DDK tag) protein expressed in sf9 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product VWF Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    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.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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.
  • Target
    VWF (Von Willebrand Factor (VWF))
    Abstract
    VWF Produkte
    Synonyme
    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
    Hintergrund
    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.
    Molekulargewicht
    67 kDa
    NCBI Accession
    NP_000543
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