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Leishmania LPG ELISA Kit

LPG Reaktivität: Leishmania Colorimetric Competition ELISA Serum
Produktnummer ABIN997045
  • Target Alle Leishmania LPG (LPG) Produkte
    Leishmania LPG (LPG) (Leishmania Lipophosphoglycan (LPG))
    Reaktivität
    Leishmania
    Nachweismethode
    Colorimetric
    Methodentyp
    Competition ELISA
    Applikation
    ELISA
    Verwendungszweck
    The Leishmania ELISA Kit is for the screening of serum antibodies, primarily IgG, for visceral Leishmania using the ELISA technique.
    Proben
    Serum
    Analytische Methode
    Qualitative
    Spezifität
    97%
    Sensitivität
    84%
  • Probenmenge
    10 μL
    Testdauer
    < 1 h
    Plattentyp
    Pre-coated
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C
    Haltbarkeit
    12 months
  • Target Alle Leishmania LPG (LPG) Produkte
    Leishmania LPG (LPG) (Leishmania Lipophosphoglycan (LPG))
    Andere Bezeichnung
    Leishmania (LPG Produkte)
    Substanzklasse
    Species
    Hintergrund
    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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