1.A multiplexed test
2.Accuracy and reliability of the results
3.Low sample input
Features
1. Simultaneous detection of seven monomorphic homopolymer biomarkersassessment
2. Fast results – 1 hourfrom sample to result
3. Evaluate results with the RapidSeq126®report software
4. Tested with paraffin-embedded samples
This RapidSeq MSI Assay is a PCR-based melting detection assay intended to qualitative detect a novel panel of seven monomorphic homopolymer biomarkers (MRE11, SULF2, RYR3, SEC31A, BTBD7, ACVR2A, and DIDO1) in formalin-fixed, paraffin-embedded (FFPE) tissue sections from human cancer tissue clinical samples. The Assay based on RapidSeq® platform automates the entire process from nucleic acids are liberated from FFPE sample, PCR amplified and melting curve assay to report of MSI status in less than 1 hour.
Biomarkers
seven monomorphic homopolymer biomarkers:
MRE11, SULF2, RYR3, SEC31A, BTBD7, ACVR2A, and DIDO1
Product Specifications
Panel
RapidSeq PHLOSS Assay of a novel panel of seven monomorphic homopolymer biomarkers
Reactions
3 times/target for a sample
Internal control
housekeeping gene GAPDH
Sample types
paraffin-embedded samples
Turnaround time
—1hour from sample to answer
To be used with
RapidSeq126®Instrument
Data analysis
RapidSeq126®report software
Scientific Background
Determination of mismatch repair (MMR) and/or microsatellite instability (MSI) status in colorectal cancer (CRC) is recommended to aid in the identification of patients with Lynch syndrome or as a prognostic indicator. In addition, it is becoming increasingly important as predictive biomarker for cancer immunotherapy.