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BPI ELISA Kit

BPI Reactivity: Human Colorimetric Competition ELISA
Catalog No. ABIN930709
  • Target See all BPI ELISA Kits
    BPI (Bactericidal/Permeability Increasing Protein (BPI))
    Reactivity
    • 3
    • 3
    • 1
    • 1
    Human
    Detection Method
    Colorimetric
    Method Type
    Competition ELISA
    Application
    ELISA
    Analytical Method
    Quantitative
    Characteristics
    ELISA kit for the detection of BPI in the research laboratory
    Alternative Names: Bactericidal permeability-increasing protein ELISA kit, BPI ELISA kit
    Top Product
    Discover our top product BPI ELISA Kit
  • Application Notes
    Optimal conditions to be determined by end-user
    Plate
    Pre-coated
    Assay Procedure

    Highly purified BPI is bound to microwells . Antibodies to this antigen, if present in diluted serum, bind in the microwells. Washing of the microwells removes unbound serum antibodies. Horseradish peroxidase (HRP) conjugated antihuman IgG immunologically bind to the bound patient antibodies forming a conjugate/antibody/antigen complex. Washing of the microwells removes unbound conjugate. An enzyme substrate in the presence of bound conjugate hydrolyzes to form a blue color. The addition of an acid stops the reaction forming a yellow endproduct. The intensity of this yellow color is measured photometrically at 450 nm. The amount of colour is directly proportional to the concentration of IgG antibodies present in the original sample.

    Restrictions
    For Research Use only
  • Storage
    4 °C
    Storage Comment
    Store at 2-8 °C.
  • Target See all BPI ELISA Kits
    BPI (Bactericidal/Permeability Increasing Protein (BPI))
    Alternative Name
    anti-BPI (BPI Products)
    Target Type
    Antibody
    Background
    The main antigen for the cANCA is the proteinase 3 (PR3), which is a serine proteinase of the present in primary granules. Antibodies of pANCA positive sera are mainly directed to myeloperoxidase (MPO). Antibodies to other antigens e.g. lactoferrin, elastase, cathepsin G and also lysozyme often result in a similar pANCA pattern. Beside different untypical variants of pANCA IF patterns granulocyte specific antinuclear antibodies (GSANA) is indistinguishable from pANCA. This makes a clear interpretation and classification of the IF patterns difficult. Therefore every positive IFANCA findings especially pANCA should be differenciated by ELISA techniques using purified antigens. A survey of documented clinical indications of specific ANCA is given in the table below. PR3ANCA and MPOANCA are reliable serologic markers in the diagnostics of vasculitides. PR3ANCA is the classical autoantigen in Wegener´s granulomatosis with a clinical specificity of more than 95 %. cANCA is documented to be present in different diseases. The target antigen myeloperoxidase is mainly present (75 %) in microscopic polyangiitis.
    Synonyms: Bactericidal permeability-increasing protein ELISA kit, BPI ELISA kit.
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