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VWF antibody

VWF Reactivity: Human IHC, ELISA, IHC (p), RIA Host: Mouse Monoclonal RFF-VIII R-1 unconjugated
Catalog No. ABIN1820041
  • Target See all VWF Antibodies
    VWF (Von Willebrand Factor (VWF))
    Reactivity
    • 147
    • 37
    • 26
    • 5
    • 4
    • 3
    Human
    Host
    • 86
    • 78
    • 12
    • 5
    Mouse
    Clonality
    • 92
    • 86
    • 1
    Monoclonal
    Conjugate
    • 91
    • 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
    • 102
    • 101
    • 68
    • 55
    • 48
    • 43
    • 25
    • 18
    • 16
    • 15
    • 14
    • 9
    • 9
    • 8
    • 8
    • 5
    • 5
    • 5
    • 4
    • 3
    • 1
    Immunohistochemistry (IHC), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Radioimmunoassay (RIA)
    Specificity
    Recognizes human von Willebrand factor (vWF), also known as Factor VIII related antigen, a blood glycoprotein involved in blood coagulation. It stabilizes circulating Factor VIII by binding to it and protecting it from cleavage and delivers it to sites of vascular injury. vWF also promotes the adhesion of platelets to sites of vascular damage by forming a molecular bridge between collagen on exposed endothelial cells and the GPIb binding sites of platelets circulating in the blood. vWF circulates in the blood as large multimers, with each monomer (250kD) containing a number of specific domains. Hereditary or acquired defects in vWF lead to von Willebrand disease (vWD), characterized by varying degrees of susceptibility to bleeding. Symptoms might include nosebleeds, bleeding gums, easy bruising, menorrhagia or gastrointestinal bleeding. Various forms of vWD exist with differing severities, determined by the type of defect. Clone RF-VIII R/1 has a high affinity for an epitope within the platelet GPIb-binding site that is responsible for biological activity. As such the antibody is a potent inhibitor of vWF activity. It can completely neutralize ristocetin-induced platelet aggregation and ristocetin-induced binding of vWF to platelets. It also inhibits platelet adhesion to glass beads. The epitope recognized is present only on the intact multimeric form of vWF and is abolished by mild denaturation with SDS. The antibody does not recognize human Factor VIII. Clone RF-VIII R/1 may be used as a capture antibody in immunoassays for vWF in combination with clone RFF-VIII R/2 as a detection reagent.
    Purification
    Protein G purified
    Immunogen
    Human Factor VIII complex partially purified from Factor VIII concentrate.
    Clone
    RFF-VIII R-1
    Isotype
    IgG1
    Top Product
    Discover our top product VWF Primary Antibody
  • Application Notes
    Approved: ELISA, IHC, IHC-P (1:50 - 1:200), RIA

    Not recommended for: WB
    Comment

    Target Species of Antibody: Human

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    PBS, 0.09 % sodium azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Storage Comment
    4°C or -20°C, Avoid freeze-thaw cycles.
  • Target
    VWF (Von Willebrand Factor (VWF))
    Alternative Name
    VWF / Von Willebrand Factor (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
    Name/Gene ID: VWF

    Synonyms: VWF, Coagulation factor VIII VWF, F8VWF, VWD, Von Willebrand factor
    Gene ID
    7450
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