Devyser’s solution for rapid prenatal aneuploidy detection

Last updated: 28th June, 2022

Products are for professional/laboratory use only.

Devyser Compact enables rapid prenatal aneuploidy detection of chromosomes 13, 18, 21 and XY in a single PCR mix.

  • Detects chromosomal aneuploidies and maternal cell contamination (MCC)
  • Single-tube PCR
  • Fast analysis with minimum hands-on time

In addition to detecting Down, Edwards, Patau and Klinefelter syndromes, the Devyser Compact kit includes our patented technology for reliable diagnosis of Turner syndrome, using two dedicated X-chromosome counting markers.

The Devyser Compact kit relies on quantitative, multiplex PCR amplification of 26 highly informative genetic markers in a single mix for rapid prenatal diagnosis of the most common autosomal and sex chromosome aneuploidies.

Features and Benefits:

  • Efficient and sensitive detection of chromosomal aneuploidies and maternal cell contamination (MCC) in DNA samples prior to microarray analysis
  • No sample mix-up. One single tube per sample during PCR and detection reduces the risk of sample mix-up.
  • Quick and easy implementation. All reagents needed to perform QF-PCR are provided in a single kit.


Introduction to QF-PCR

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Detecting mosaicism with QF-PCR

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QF-PCR and maternal cell contamination

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QF-PCR in pregnancy loss analysis

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