Kalazar Detect™ Rapid Test for Visceral Leishmaniasis

FDA Cleared for In Vitro Diagnostic Use

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The Kalazar Detect™ Rapid Test for Visceral Leishmaniasis (VL) is a rapid immunochromatographic strip assay for the qualitative detection of antibodies to members of L. donovani in human serum to aid in the presumptive diagnosis of VL.

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  • US FDA Cleared

  • CE Marked

  • Relative Sensitivity and Relative Specificity: >90%

  • Fast Results: 10 minutes

  • Field Friendly: Refrigeration and lab equipment not required

Catalog No. INS025
Format ICT (strip)
Quantity/Kit 25 tests
Time to Result 10 minutes
Sample Type Serum
Storage Room Temperature (20°C-30°C)
Shelf Life 24 months

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Matlashewski G, Das VNR, Pandey K, Singh D, Das S, Ghosh AK, et al. (2013) Diagnosis of Visceral Leishmaniasis in Bihar India: Comparison of the rK39 Rapid Diagnostic Test on Whole Blood Versus Serum. PLoS Negl Trop Dis 7(5): e2233. doi:10.1371/journal.pntd.0002233

Carvalho SF, Lemos EM, Corey R, Dietze R. Performance of recombinant K39 antigen in the diagnosis of Brazilian visceral leishmaniasis. American Journal of Tropical Medicine and Hygiene.2003;68((3)):321–4.

WHO Visceral Leishmaniasis Rapid Diagnostic Test Performance Report

Welch, R. J., Anderson, B. L., & Litwin, C. M. (2008). Rapid Immunochromatographic Strip Test for Detection of Anti-K39 Immunoglobulin G Antibodies for Diagnosis of Visceral Leishmaniasis . Clinical and Vaccine Immunology : CVI, 15(9), 1483–1484. http://doi.org/10.1128/CVI.00174-08 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546669/)

For more information, download the instructions for use via the “Downloads” tab.

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