Devyser’s solution for rapid prenatal aneuploidy detection

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.

THESE PRODUCTS ARE NOT AVAILABLE FOR PURCHASE BY THE GENERAL PUBLIC.

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