Features & Benefits
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Efficient and sensitive detection of chromosomal aneuploidies and maternal cell contamination (MCC) in DNA samples prior to microarray analysis
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No sample mix-up. One single tube per sample during PCR and detection reduces the risk of sample mix-up.
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Quick and easy implementation. All reagents needed to perform QF-PCR are provided in a single kit.
Devyser Compact
Devyser Compact enables rapid prenatal aneuploidy detection of chromosomes 13, 18, 21 and XY in a single PCR mix. 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.
For further information on the Devyser Compact Kit, click here.
To download the Devyser Compact Kit handbook, click here.
Features & Benefits
Analysis is performed using two separate PCR mixes including cross mix ID markers in both mixes to reduce the risk of sample mix-up. Devyser Complete is used to detect Down, Edwards, Patau and Klinefelter syndromes. It also includes Devyser's patented technology for detection of Turner syndrome, using two dedicated X-chromosome counting markers.
Devyser Complete
Devyser Complete enables rapid prenatal aneuploidy detection of chromosomes 13, 18, 21 and XY. Includes analysis of 33 genetic markers. It is suitable for laboratories that frequently analyze samples that require analysis of a large numbers of markers to reduce reflex testing.
For further information on the Devyser Complete, click here.
To download the Devyser Complete handbook, click here.
Features & Benefits
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No tissue culture needed
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Eliminate cell culture, increase analysis success rates and speed up pregnancy loss aneuploidy analysis
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Results in less than 5 hours
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Includes 42 genetic markers for aneuploidy analysis by QF-PCR of chromosomes 13, 15, 16, 18, 21, 22, X and Y. Two unique X-chromosome counting markers for reliable detection of Turner syndrome are also included
Devyser Extend
Devyser Extend enable rapid aneuploidy analysis of chromosomes 13, 15, 16, 18, 21, 22, X and Y.
For further information on the Devyser Extend, click here.
To download the Devyser Extend handbook, click here.
Features & Benefits
Suitable for rapid reflex testing of STR markers on chromosome 13 when additional informative markers are needed for conclusive results
Devyser Resolution 13
Devyser Resolution 13 is a rapid quantitative analysis for stand alone, resolution or reflex testing of chromosome 13.
For further information on the Devyser Resolution 13, click here.
To download the Devyser Resolution 13 handbook, click here.
Features & Benefits
Suitable for rapid reflex testing of STR markers on chromosome 18 when additional informative markers are needed for conclusive results.
Devyser Resolution 18
Devyser Resolution 18 is a rapid quantitative analysis for stand alone, resolution or reflex testing of chromosome 18.
For further information on the Devyser Resolution 18, click here.
To download the Devyser Resolution 18 handbook, click here.
Features & Benefits
Suitable for rapid reflex testing of STR markers on chromosome 21 when additional informative markers are needed for conclusive results
Devyser Resolution 21
Devyser Resolution 21 is a rapid quantitative analysis for stand alone, resolution or reflex testing of chromosome 21.
For further information on the Devyser Resolution 21, click here.
To download the Devyser Resolution 21 handbook, click here.
Features & Benefits
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Requires minimal amounts of genomic DNA
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Results in less than five hours
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Suitable for rapid reflex testing of STR markers on chromosomes X and Y when additional informative markers are needed for conclusive results
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Suitable for stand alone diagnosis of Turner (45, X) and Klinefelter syndrome (47, +XXY) in aneuploidy and infertility investigations
