ChromoQuant^® QF-PCR kits are a family of products for fast 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 X and Y, i.e. Klinefelter syndrome and Turner syndrome.

 

The tests have been clinically validated for In Vitro Diagnostics and are CE marked.

• The diagnostic procedure is based upon amniocentesis. Results are achieved within 6 hours enabling a "time to reply" of 24 hours
• ^®The ChromoQuant kit is validated for ABI and MegaBACE sequencers. Diagnostic procedures based on ChromoQuant® can be automated for cost efficient high throughput analysis.
• ChromoQuant® is CE marked for IVD use and produced according to ISO13485:2003 and ISO 9001:2008. 
• Fast data evaluation is facilitated by the proprietary ChromoQuant^® Visualizer software licensed to all users.

ChromoQuant^® was clinically introduced in early 2004 and is used world wide. More than 44.000 clinical tests have been performed with the ChromoQuant test since 2004 (october 2009).

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