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VWF anticorps

VWF Reactivité: Humain IHC, ELISA, IHC (p), RIA Hôte: Souris Monoclonal RFF-VIII R-1 unconjugated
N° du produit ABIN1820041
  • Antigène Voir toutes VWF Anticorps
    VWF (Von Willebrand Factor (VWF))
    Reactivité
    • 151
    • 39
    • 26
    • 6
    • 5
    • 3
    Humain
    Hôte
    • 86
    • 78
    • 16
    • 9
    Souris
    Clonalité
    • 94
    • 92
    • 1
    Monoclonal
    Conjugué
    • 95
    • 21
    • 15
    • 9
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp VWF est non-conjugé
    Application
    • 110
    • 101
    • 72
    • 55
    • 52
    • 51
    • 25
    • 18
    • 16
    • 15
    • 14
    • 9
    • 9
    • 9
    • 8
    • 8
    • 5
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 1
    Immunohistochemistry (IHC), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Radioimmunoassay (RIA)
    Specificité
    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
    Immunogène
    Human Factor VIII complex partially purified from Factor VIII concentrate.
    Clone
    RFF-VIII R-1
    Isotype
    IgG1
    Top Product
    Discover our top product VWF Anticorps primaire
  • Indications d'application
    Approved: ELISA, IHC, IHC-P (1:50 - 1:200), RIA

    Not recommended for: WB
    Commentaires

    Target Species of Antibody: Human

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    PBS, 0.09 % sodium azide
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    4°C or -20°C, Avoid freeze-thaw cycles.
  • Antigène
    VWF (Von Willebrand Factor (VWF))
    Autre désignation
    VWF / Von Willebrand Factor (VWF Produits)
    Synonymes
    anticorps VWF, anticorps si:ch1073-474e24.1, anticorps F8VWF, anticorps VWD, anticorps 6820430P06Rik, anticorps AI551257, anticorps B130011O06Rik, anticorps C630030D09, anticorps von Willebrand factor, anticorps Von Willebrand factor, anticorps VWF, anticorps vwf, anticorps Vwf
    Sujet
    Name/Gene ID: VWF

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