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ACA-IgA ELISA Kit

Dieses Colorimetric ELISA-Kit wurde entwickelt für die quantitative Messung von Human ACA-IgA.
Produktnummer ABIN1326803

Kurzübersicht für ACA-IgA ELISA Kit (ABIN1326803)

Target

Alle ACA-IgA Produkte
ACA-IgA (Anti-Cardiolipin Antibody IgA (ACA-IgA))

Reaktivität

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Human

Nachweismethode

Colorimetric

Methodentyp

Competition ELISA

Applikation

ELISA

Proben

Serum
  • Verwendungszweck

    Diluted patient serum is added to wells coated with purified aCL antigen. aCL specific IgA antibody, if present, binds to the antigen. All unbound materials are washed away and the enzyme conjugate is added to bind to the antibody-antigen complex, if present. Excess enzyme conjugate is washed off and substrate is added. The plate is incubated to allow the hydrolysis of the substrate by the enzyme. The intensity of the color generated is proportional to the amount of specific antibody in the sample.

    Analytische Methode

    Qualitative
  • Plattentyp

    Pre-coated

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    4 °C
  • Target Alle ACA-IgA Produkte

    ACA-IgA (Anti-Cardiolipin Antibody IgA (ACA-IgA))

    Andere Bezeichnung

    Cardiolipin IgA

    Substanzklasse

    Antibody

    Hintergrund

    Measurement of IgG, IgM and IgA cardiolipin autoantibodies (aCL) by EIA is the standard procedure for the detection of antiphospholipid antibodies (aPL) in patients with suspected antiphospholipid syndrome (APS).High aCL concentrations are associated with increased risk of venous and arterial thrombosis, recurrent pregnancy loss and thrombocytopenia. Patients with the anti-cardiolipin syndrome have one of the above clinical features and have antibodies to cardiolipin andor a positive lupus anticoagulant test. The antibodies present to cardiolipin may be of the IgG, IgA, IgM isotypes.Testing for the various antibody isotypes to cardiolipin aid in diagnosis of the anti-phospholipid syndrome in patients with SLE or lupus-like disorders. Binding of aCL to CL in patients with autoimmune diseases is dependent on the presence of the cofactor ibetai-2-glycoprotein I (ibetasub2subi-GPI) this binding is independent of ibetai-2-GPI in patients with infectious diseases (e.g., syphilis, tuberculosis). Recognition of the role of ibetai-2-GPI in the binding of aCL led to development of assay for direct measurement of ibetai-2-GPI autoantibodies using ibetai-2-GPI as antigen,allowing a clear distinction between ibetai-2-GPI autoantibodies and those that bind to CL alone.
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