Part 1. mRNA characterization U U U U U U Direct mRNA Sequence Confirmation End-to-end LC-HRAM MS solution U U U U U U U mRNA U U U U U U U U U U U RNase T1 U U U U U U Reproducible, controlled partial digestion using immobilized RNAse magnetic beads. U U U 100 U U U U U RNA-Seq is the most common technology * Indirect. mRNA needs to be converted into DNA. U U U U U U U U U * Library/primer design is needed for each mRNA. U U U U U U U * Analysis takes >2 days. * Multi-step, multi-instrument process. An innovative LC-HRAM MS workflow * Direct measurement of mRNA. * Universal, no need for library/primer. * Fast (~2 hr), reproducible. * Accurate, comprehensive sequence coverage (>85%). * End-to-end solution with automation. Confident, comprehensive sequence identification. GENengnews.com | 29 U U U U U U U U U U 5 10 15 20 RT (min) 25 30 35 40 High-resolution separation and high-quality MS, MS/MS data. U U 10 20 30 40 50 60 70 80 90 U U U U 4.77 5.17 10.7611.78 9.66 6.51 8.08 9.00 14.81 15.80 29.60 13.99 U 24.96 U U 17.97 17.22 20.73 18.73 19.70 26.70 27.64 31.81 33.24 34.08 34.8936.09 39.49 40.66 U U 23.69 U U U 28.30 U U U U U U U U U U U U U U U U U U U U U 22.78 U U U U U Relative intensity U U U U U U U U U U U U U U U U U U U U U U U U U U U U U U U U U U U Uhttps://www.thermofisher.com/us/en/home.html https://www.genengnews.com