Leishmania LPG ELISA Kit

Produktnummer ABIN997045

Leishmania Leishmania LPG ELISA-Kit Colorimetric-Assay zur Quantifizierung von Leishmania Leishmania LPG.

Kurzübersicht für Leishmania LPG ELISA Kit (ABIN997045)

Target: Leishmania LPG (LPG) (Leishmania Lipophosphoglycan (LPG))

Reaktivität: Leishmania

Nachweismethode: Colorimetric

Methodentyp: Competition ELISA

Applikation: ELISA

Proben: Serum

Produktdetails Leishmania LPG ELISA Kit

Verwendungszweck: The Leishmania ELISA Kit is for the screening of serum antibodies, primarily IgG, for visceral Leishmania using the ELISA technique.

Analytische Methode: Qualitative

Spezifität: 97%

Sensitivität: 84%

Anwendungsinformationen

Probenmenge: 10 μL

Testdauer: < 1 h

Plattentyp: Pre-coated

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Lagerung: 4 °C

Haltbarkeit: 12 months

Details zu Leishmania LPG

Target: Leishmania LPG (LPG) (Leishmania Lipophosphoglycan (LPG))

Andere Bezeichnung: Leishmania

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.