ChromoQuant® QF-PCR work flow
ChromoQuant Family brochure
ChromoQuant 513 STaR brochure / analysis of aneuploidies in chromosomes 13, 18, 21 and X, Y – single tube
ChromoQuant 311 brochure /analysis of aneuploidies in chromosomes 13, 18, 21 and X, Y
ChromoQuant 412 brochure /analysis of aneuploidies in chromosomes 13, 18, 21
ChromoQuant Visualizer brochure /decision support and database Software
1.DNA extraction from e.g. amniotic fluid
3.Capillary Electrophoresis (ABI or MegaBACE systems)
4.Export of data and Diagnosis
From amniotic fluid to diagnosis within a working day!
ChromoQuant® QF-PCR kits is a family of products for fast and reliable diagnosis of the most common chromosomal disorders in foetuses.
ChromoQuant® detects Trisomy 21 (Down syndrome), Trisomy 13 (Patau syndrome), Trisomy 18 (Edwards syndrome) and aneuploidies in the sex chromosomes i.e. Klinefelter syndrome and Turner syndrome.
Decision support software for objective and fast interpretation of results, Visualizer™ is licenced to all users. Visualizer™ is also a database for safe storing and traceability of data.
ChromoQuant® is validated for In Vitro Diagnostics and CE marked in accordance to ISO 13485-2003 and ISO 9001-2000.