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Legionella IgG/IgM/IgA ELISA Kit

Das Borrelia burgdorferi Legionella IgG/IgM/IgA ELISA Kit (ABIN997005) ist ein Colorimetric ELISA Kit zur Detektion von Borrelia burgdorferi Legionella IgG/IgM/IgA.
Produktnummer ABIN997005
675,71 €
Zzgl. Versandkosten 20,00 € und MwSt
96 tests
Lieferung nach: Deutschland
Lieferung in 20 bis 27 Werktagen

Kurzübersicht für Legionella IgG/IgM/IgA ELISA Kit (ABIN997005)

Target

Legionella IgG/IgM/IgA

Reaktivität

Borrelia burgdorferi

Nachweismethode

Colorimetric

Methodentyp

Competition ELISA

Applikation

ELISA
  • Verwendungszweck

    Legionella IgG/IgM/IgA ELISA Test System is an enzyme-linked immunosorbent assay for the qualitative detection of total antibody (IgG/IgM/IgA) to Legionella pneumophila serogroups 1-6 in human sera.

    Analytische Methode

    Qualitative

    Spezifität

    93.1%

    Sensitivität

    92.3%
  • Probenmenge

    10 μL

    Testdauer

    1 - 2 h

    Plattentyp

    Pre-coated

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    4 °C

    Haltbarkeit

    12-18 months
  • Target

    Legionella IgG/IgM/IgA

    Andere Bezeichnung

    Legionella G/M/A

    Substanzklasse

    Antibody

    Hintergrund

    L. pneumophila was identified as the causative agent for Legionellosis (Legionella pneumonia, or Legionnaire's Disease) in 1977. Presently, there are more than 25 species and 33 serogroups in the family Legionellaceae, with at least 18 species associated with pneumonia, accounting for roughly 1-5% of all cases of pneumonia. L. pneumophila displays a multitude of morphologies including the bacillus, coccobacillus, and elongated fusiform. Although often difficult to perform, the Gram stain will be Gram-negative. The antibody response to L. pneumophila may be both specific and nonspecific, since the patient may have antibodies to similar antigens from other Gram-negative bacteria. Optimum times for specimen collection appear to be within the first week of illness, or as soon as possible after the onset (acute specimen), and at least 3 weeks after the onset (convalescent specimen). By the IFA method, a single result of 1:256 is considered presumptive evidence of legionella infection. Diagnostic titers have been reported to be absent in as many as 25% of patients, but the use of multiple Legionella species as the antigen source and a polyvalent conjugate directed against IgG, IgM, and IgA maximize the accuracy of serological procedures.
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