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Myeloperoxidase ELISA Kit

This Colorimetric ELISA kit is designed for the quantitative measurement of Human Myeloperoxidase.
Catalog No. ABIN930701

Quick Overview for Myeloperoxidase ELISA Kit (ABIN930701)

Target

See all Myeloperoxidase (MPO) ELISA Kits
Myeloperoxidase (MPO)

Reactivity

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Human

Detection Method

Colorimetric

Method Type

Competition ELISA

Application

ELISA
  • Analytical Method

    Quantitative

    Characteristics

    ELISA kit for the detection of MPO in the research laboratory
    Alternative Names: Myeloperoxidase ELISA kit, MPO ELISA kit
  • Application Notes

    Optimal conditions to be determined by end-user

    Plate

    Pre-coated

    Assay Procedure

    Highly purified myeloperoxidase (MPO) 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 Myeloperoxidase (MPO) ELISA Kits

    Myeloperoxidase (MPO)

    Alternative Name

    MPO

    Target Type

    Disease

    Background

    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 (cANCA) and a perinuclear (pANCA) type. 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 finding esp. pANCA should be differenciated by ELISA techniques using purified antigens. 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: Myeloperoxidase ELISA kit, MPO ELISA kit.

    Pathways

    Chromatin Binding
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