The fully automated IdyllaTM ctNRAS-BRAF-EGFR S492R Mutation Assay is minimally invasive, fast and easy to perform. ctNRAS-BRAF-EGFR S492R covers 18 mutations in NRAS exons 2,3 and 4, 5 mutations in BRAF codon 600 as well as 2 EGFR mutations in codon 492 and showed an high concordance of 100% for NRAS as well as 99.5% for BRAF compared to NGS using plasma samples from 198 mCRC patients enrolled in the prospective multicenter RASANC study.
More info: IdyllaTM ctNRAS-BRAF-EGFR S492R
ctNRAS-BRAF Technical sheet