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Legionella IgG/IgM/IgA Kit ELISA

Le kit ELISA Legionella IgG/IgM/IgA (ABIN997005) Borrelia burgdorferi est un kit ELISA Colorimetric conçu pour quantifier Borrelia burgdorferi Legionella IgG/IgM/IgA.
N° du produit ABIN997005
675,71 €
Plus frais de livraison 40,00 € et TVA
96 tests
Destination: France
Envoi sous 20 à 27 jours ouvrables

Aperçu rapide pour Legionella IgG/IgM/IgA Kit ELISA (ABIN997005)

Antigène

Legionella IgG/IgM/IgA

Reactivité

Borrelia burgdorferi

Méthode de détection

Colorimetric

Type de méthode

Competition ELISA

Application

ELISA
  • Fonction

    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.

    Analytical Method

    Qualitative

    Specificité

    93.1%

    Sensibilité

    92.3%
  • Volume d'échantillon

    10 μL

    Durée du test

    1 - 2 h

    Plaque

    Pre-coated

    Restrictions

    For Research Use only
  • Stock

    4 °C

    Date de péremption

    12-18 months
  • Antigène

    Legionella IgG/IgM/IgA

    Autre désignation

    Legionella G/M/A

    Classe de substances

    Antibody

    Sujet

    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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