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Rapid Diagnosis of Trisomy 13, 18, 21 and Sex Chromosome Aneuploidies

  • CE/IVD product, manufactured to ISO13485:2016
  • Sample to result in less than 3 hours
  • Optimised to work on capillary electrophoresis genetic analysers
  • Kit contains 36 markers for detection of Trisomy 21 (Down’s Syndrome), Trisomy 18 (Edwards Syndrome), Trisomy 13 (Patau Syndrome) and XY chromosomes aneuploidies, including X monosomy (Turner Syndrome), and XXY (Klinefelter Syndrome).
  • The kit also includes four chromosome-specific marker sets (M21, M13, M18 and MXY)
  • Five Dye-Labelling allows simultaneous analysis of several loci in a single electrophoresis
  • Only QF-PCR test on the market with 4 pseudoautosomal markers for XY aneuploidies and mosaic cases
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