Anyplex™ II Thrombosis SNP Panel Assay simultaneously detects and discriminates 6 SNPs (1 in Factor II, 3 in Factor V and 2 in MTHFR) that are the most important genetic risk factors of venous thrombosis. Based on mTOCE™ technology, this assay detects and differentiates multiple SNPs without performance being affected by in a single channel using real-time PCR.
Multiple SNPs are detected and differentiated in a single channel
Performance is not affected by multiple SNPs being present
7 SNPs in Factor II, Factor V and MTHFR genes can be detected in a single tube
Utilization of the UDG system to prevent carry-over contamination
Automated data interpretation and LIS interlocking with Seegene Viewer
Quick and proper treatment provided by accurate test results
Automated data interpretation and LIS interlocking with Seegene Viewer
Whole process validation from extraction to PCR by whole process control
Convenient workflow using Seegene’s automated one platform
The results indicate multiple results of H1299R (Heterozygote type), C677T (Homozygote type), R506Q (Wild type) in the FAM / HEX channel, and G20210A (Heterozygote type) in the Cal Red 610 / Quasar 670 channels