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Leishmania IgG Kit ELISA

Kit ELISA Leishmania IgG Humain, Colorimetric test pour la quantification de Humain Leishmania IgG.
N° du produit ABIN997045
433,71 €
Plus frais de livraison 40,00 € et TVA
96 tests
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour Leishmania IgG Kit ELISA (ABIN997045)

Antigène

Leishmania IgG

Reactivité

Humain

Méthode de détection

Colorimetric

Type de méthode

Indirect ELISA

Application

ELISA

Type d'échantillon

Serum
  • Fonction

    The Leishmania infantum IgG ELISA is intended for the qualitative determination of IgG class antibodies against Leishmania infantum in human serum or plasma (citrate, heparin).

    Analytical Method

    Qualitative

    Specificité

    92.59%

    Sensibilité

    90.91%
  • 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 months
  • Antigène

    Leishmania IgG

    Classe de substances

    Species

    Sujet

    Visceral Leishmaniasis (VL) is a severe disease with high mortality, caused by parasite members of the L. donovani complex. The vector for transmission is the sand fly, whose carriers of infection are typically dogs. It is a disease endemic to many countries and is a serious problem in many developing nations, particularly with the increasing urbanization of populations. High incidence is encountered in parts of Latin America, East Africa, Middle East, India and China. It is endemic to countries bordering the Mediterranean such as Italy, Southern France, Spain, Portugal, and Northern Africa. In Southern Europe, VL has become the leading opportunistic infection in AIDS patients. Diagnosis of acute VL is often attempted by aspiration of bone marrow for direct parasite identification. The procedure is invasive, painful, dangerous and has a low success rate due to the inability to always isolate parasites from the tissue. Alternatively, serodiagnosis is widely utilized since anti-leishmanial antibody titers are typically high during the acute disease phase. ELISA is the preferred laboratory test for serodiagnosis of VL, although indirect immunofluorescent antibody tests (IFAT) and direct agglutination tests (DAT), using whole parasites, are still widely used in conjunction with ELISA or alone.
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