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VWF Protein (DYKDDDDK Tag)

VWF Origin: Human Host: Insect cells (Sf9) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2735406
  • Target See all VWF Proteins
    VWF (Von Willebrand Factor (VWF))
    Protein Type
    Recombinant
    Origin
    • 4
    • 4
    • 4
    • 2
    • 2
    • 1
    Human
    Source
    • 12
    • 2
    • 1
    • 1
    • 1
    Insect cells (Sf9)
    Purification tag / Conjugate
    This VWF protein is labelled with DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human von Willebrand factor (VWF) (C-term DDK tag) protein expressed in sf9 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product VWF Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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 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
    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.
    Molecular Weight
    67 kDa
    NCBI Accession
    NP_000543
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