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ANCA-C (PR3) ELISA

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產品名稱: ANCA-C (PR3) ELISA
產品型號: DE7060
產品展商: 原裝進口
產品文檔: 無相關文檔

簡單介紹

ANCA-C (PR3) ELISA


ANCA-C (PR3) ELISA  的詳細介紹
ANCA-C (PR3) ELISA

產品名稱:ANCA-C (PR3) ELISA
產    地:Demeditec
產品貨號:DE7060
產品規格:96 Tests
產品說明:
Special remarks:
Anti-PR3 is an indirect solid phase enzyme immunoassay (ELISA) for the quantitative measurement of IgG class autoantibodies against proteinase 3 (PR3) in human serum or plasma. The assay is intended for in vitro diagnostic use only as an aid in the diagnosis of certain autoimmune vasculitides such as Wegener´s granulomatosis.
Anti-neutrophilic-cytoplasm antibodies (ANCA) represents a group of autoantibodies directed towards the cytoplasmatic components of the neutrophilic granulocytes and monocytes. The classical methods for the determination of ANCA are the immunofluorescent methods. With these indirect immunofluorescence techniques two main patterns are recognized, a cytoplasmatic (c-ANCA) and a perinuclear (p-ANCA) type.
The main antigen for the c-ANCA is the proteinase 3 (PR3), which is a serine proteinase of the present in primary granules. Antibodies of p-ANCA 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 p-ANCA pattern. Beside different untypical variants of p-ANCA IF patterns granulocyte specific antinuclear antibodies (GS-ANA) is indistinguishable from p-ANCA. This makes a clear interpretation and classification of the IF patterns difficult. Therefore every positive IF-ANCA findings esp. p-ANCA should be differenciated by ELISA techniques using purified antigens.
A survey of documented clinical indications of specific ANCA is given in the table below. PR3-ANCA and MPO-ANCA are reliable serologic markers in the diagnostics of vasculitides. PR3-ANCA is the classical autoantigen in Wegener´s granulomatosis with a clinical specificity of more than 95%. c-ANCA is documented to be present in different diseases. The target antigen myeloperoxidase is mainly present (70%) in microscopic polyangiitis.
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