Find a product for my lab

Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
Devyser Placeholder
2 Large
1 Apricot
Devyser Thalassemia NGS
Complete single-tube analysis for thalassemias
Fast and simple NGS workflow
User-friendly data analysis software
View product
1 Medium
1 Apricot
Devyser FH NGS
Comprehensive gene panel for Familial hypercholesterolemia (FH)
Identify 12 SNPs in polygenic FH & the 6 SNPs to predict statin response
Single-tube workflow for fast results
View product
1 Medium
1 Apricot
Devyser Thrombophilia
One single mix for testing of six relevant risk factors for thrombophilia
Single-tube PCR
Fast analysis with minimum hands-on time
View product
2 Large
0 Yellow
Devyser CFTR NGS
Full CFTR gene sequencing
Single-tube NGS library prep kit
CE-IVD
View product
2 Large
3 Pink
Devyser CFTR 68
Detects 68 CFTR mutations
Allele-specific detection
CE-IVD
View product
1 Medium
3 Pink
Devyser CFTR Core
Detects the 36 most common mutations found in populations of European origin
Allele-specific detection of wild-type and variants
View product
1 Medium
3 Pink
Devyser CFTR Italia
Designed for the Italian population
Detects the normal and mutant alleles at 31 loci of the CFTR gene
Includes ID markers for sample identity confirmation
View product
1 Medium
2 Purple
Devyser HFE
Multiplex detection of the three most important HFE mutations and the corresponding wild types
Single-tube PCR
Accurate and efficient
View product
1 Medium
2 Purple
Devyser CVD
Detects seven risk factors for cardiovascular disease
Single-tube PCR
Fast analysis with minimum hands-on time
View product
Devyser Placeholder

Devyser Placeholder

Hereditary

Devyser offers a broad panel of allele-specific and NGS-based test kits for hereditary diseases.

Contact me

Devyser’s test kits are used to detect genetic variants associated with a wide variety of genetic disorders including thalassemia, cystic fibrosis, familial hypercholesterolemia and thrombophilia. Results may be used by clinicians to guide patient treatment and management.

Related articles

Whitepaper: NGS: Changing the game in CFTR analysis

Booklet: Devyser Thalassemia

Whitepaper: Familial hypercholesterolemia: Genetic diagnosis and cascade testing using NGS

No items found.