Products are for professional/laboratory use only.
Reduce hands-on time from days to minutes with Devyser’s single tube, next-generation sequencing (NGS) library prep kit for fast and complete characterisation of BRCA1 and BRCA2.
- Detect all mutations in BRCA1 and BRCA2
- One tube per patient sample, no sample splitting
- Less than 45 minutes hands-on time
NGS has never been easier
The Devyser BRCA kit is easy to implement and highly cost-effective, making it a good match for laboratories of any size. With ready-to-use reagents and a user-friendly workflow, it suits both manual and automated workflows. Devyser’s unique single-tube approach simplifies the workflow, reduces hands-on time and minimises the risk of sample mix-up and contamination.
The proprietary multiplex PCR primer chemistry provides full and uniform coverage of BRCA1 and BRCA2, covering all exons and exon/intron junctions. The kit uses overlapping primer design to ascertain superior INDEL coverage and downstream CNV* analysis. The Devyser BRCA kit can be used to detect both germline and somatic mutations.
Quick and easy implementation
With ready-to-use reagents, less than 45 minutes hands-on time and customised data interpretation software, it is a good match for laboratories of any size. The targeted sequencing approach combined with uniform coverage of target regions maximises the output of relevant sequencing data in every run.
Analytical software options
Laboratories have a choice of fully validated analytical software solutions, locally deployed or cloud-based. Devyser also support integration with other analytical software solutions.
Products are for Research Use Only in Australia.
*CNV detection is not validated for FFPE samples
