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VWF anticorps

VWF Reactivité: Humain IP Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN458118
  • Antigène Voir toutes VWF Anticorps
    VWF (Von Willebrand Factor (VWF))
    Reactivité
    • 150
    • 39
    • 26
    • 6
    • 5
    • 3
    Humain
    Hôte
    • 85
    • 78
    • 16
    • 9
    Lapin
    Clonalité
    • 93
    • 92
    • 1
    Polyclonal
    Conjugué
    • 94
    • 21
    • 15
    • 9
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp VWF est non-conjugé
    Application
    • 110
    • 101
    • 72
    • 55
    • 51
    • 51
    • 25
    • 18
    • 16
    • 15
    • 14
    • 9
    • 9
    • 9
    • 8
    • 8
    • 5
    • 5
    • 4
    • 4
    • 4
    • 4
    • 3
    • 1
    Immunoprecipitation (IP)
    Specificité
    The antiserum does not cross-react with any other human plasma proteins as tested in gel-diffusion techniques. Inter-species cross-reactivity is a normal feature of antibodies to plasma proteins, since homologous proteins of different species frequently share antigenic determinants. of this antiserum has not been tested in detail.
    Attributs du produit
    Precipitating polyclonal rabbit antiserum to human Von Willebrand Factor (FVIII VWF)
    Purification
    Adsorption: Immunoaffinity adsorbed using insolubilized antigens as required, to eliminate antibodies reacting with other human serum proteins. The use of insolubilized adsorption antigens prevents the presence of excess adsorbent protein or immune complexes in the antiserum.
    Immunogène
    Human FVIII procoagulant activity (FVIIIC) is carried by a polypeptide non-covalently bound to a large carrier molecule (unit molecular weight 250 kD) known as the Von Willebrand factor (VWF). FVIII/VWF exists in plasma as a series of polymers with molecular weights > 1.100 kD. FVIIIC is probably formed in the liver, is unstable on storage but sufficiently stable in fresh frozen plasma as cryoprecipitate or FVIII concentrate. VWF is synthesized in megakaryocytes and vascular endothelial cells, it is also present in the alpha-granules and membranes of platelets, binding to specific sites on the activated platelet after its release. It is responsible for platelet adhesion to the vascular subendothelium. FVIIIC, but not VWF is completely consumed during coagulation ad is absent from serum. Polyclonal antisera are raised against FVIII/VWF purified from plasma. Freund’s complete adjuvant is used in the first step of the immunization procedure.
    Isotype
    IgG
    Top Product
    Discover our top product VWF Anticorps primaire
  • Indications d'application
    It is strongly recommended to perform the EID-assay with the special agarose High Resolution Buffer and High resolution-buffered Agarose, performance tested to assure reliable and reproducible results. The threshold of detection in this technique is about 0.15 mg per 100 ml. Haemophilia A and Von Willebrand’s disease (VWD) are known to be FVIII/VWF deficiencies. Immunologic determination of VWF antigen enables to discriminate between these two bleeding conditions. Haemophilia A patients lack FVIIIC but have a normal level of VWFag. In VWD, both FVIIIC and VWFag are reduced. Active and inactive FVIII/VWF, its breakdown products and inactivated FVIII/VWF-inhibitor complexes all express antigen determinants of VWFag and may be recognized by polyclonal antisera. Determination f plasma VWFag levels in addition to the level of FVIIIC can contribute also to the detection of the carrier state in haemophilia A. While the level of VWFag is normal or even elevated, the average concentration of FVIIIC of carriers is about half of normal. Various types and subtypes of congenital VWD have been described. Cases of acquired VWD have been reported in association with several clinical diseases including autoimmune disease, systemic lupus erythematosus, benign monoclonal gammapathy and Waldenström’s macroglobulinemia.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    IgG protein concentration in the antiserum is 10 mg/ml. No foreign proteins added. Antibody titre: The antiserum is standardized for use in the electroimmunodiffusion (EID, Laurell) test procedure for the quantitative determination of FVIII/VWF as scribed
    Buffer
    Delipidated, heat inactivated, lyophilized, stable whole serum.
    Agent conservateur
    Without preservative
    Stock
    4 °C/-20 °C
    Stockage commentaire
    The lyophilized antiserum is shipped at ambient temperature and may be stored at +4°C, prolonged stora ge at or below -20°C. Reconstitute the lyophilized antiserum by add ing 1 ml sterile distilled water. Dilutions may be prepared by adding phosphate buffered saline (PBS, pH 7.2). Repeated thawing and freezing should be avoided. If a slight precipitation occurs upon storage, this should be removed by centrifugation. It will not affect the performance of the antiserum. Diluted antiserum should be stored at +4°C, not refrozen, and preferably used the same day.
  • Antigène
    VWF (Von Willebrand Factor (VWF))
    Autre désignation
    Von Willebrand Factor (FVIII VWF) (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
    The defined antibody reactivity is restricted to VWF. In immunoelectrophoresis, bi-dimensional electrophoresis and radial immunodiffusion (Ouchterlony) against normal plasma, a single precipitin line is obtained which shows a reaction of identity with precipitated purified FVIII/VWF. No precipitation is obtained with plasma of type 1 congenital Von Willebrand’s disease
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