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VWF antibody

VWF Reactivity: Human IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2428914
  • Target See all VWF Antibodies
    VWF (Von Willebrand Factor (VWF))
    Reactivity
    • 150
    • 37
    • 26
    • 5
    • 4
    • 3
    Human
    Host
    • 86
    • 81
    • 12
    • 5
    Rabbit
    Clonality
    • 95
    • 86
    • 1
    Polyclonal
    Conjugate
    • 94
    • 20
    • 15
    • 6
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This VWF antibody is un-conjugated
    Application
    • 104
    • 101
    • 70
    • 57
    • 49
    • 43
    • 28
    • 18
    • 16
    • 15
    • 14
    • 9
    • 9
    • 8
    • 8
    • 5
    • 5
    • 5
    • 4
    • 3
    • 1
    Immunohistochemistry (IHC), ELISA
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human VWF
    Isotype
    IgG
    Top Product
    Discover our top product VWF Primary Antibody
  • Application Notes
    IHC 1:25-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    VWF (Von Willebrand Factor (VWF))
    Alternative Name
    VWF (VWF Products)
    Synonyms
    VWF antibody, si:ch1073-474e24.1 antibody, F8VWF antibody, VWD antibody, 6820430P06Rik antibody, AI551257 antibody, B130011O06Rik antibody, C630030D09 antibody, von Willebrand factor antibody, Von Willebrand factor antibody, VWF antibody, vwf antibody, Vwf antibody
    Background
    The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22.
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