Monitoring RNA fusions like BCR-ABL1 is essential for tracking molecular response and minimal residual disease (MRD) in chronic myeloid leukemia.

Legacy RT–qPCR and digital PCR technologies demand multiple sample transfers, standard curves, and replicate wells — consuming valuable patient material, adding hands-on time, and increasing cost.

Meet the RNA Module for Countable PCR — a one-step workflow for RNA fusion detection that

• Merges reverse transcription, PCR, and counting in a single tube
• Eliminates multiple sample transfers and replicates 
• In combination with Countable PCR, it provides direct and reproducible molecular counts without a standard curve

In this webinar, you’ll learn how the RNA Module was used to

• Achieve direct RNA counting to simplify analysis while expanding dynamic range and accuracy
• Quantify multiple BCR–ABL1 isoforms and reference ABL1 in a single reaction with down to 0.003% IS sensitivity
• Reduce transfers, reagents, and replicate wells to save both sample and cost

This webinar is for you if you are a translational and clinical researcher developing or refining RNA-based MRD assays and need a solution with a faster, more precise, and cost-effective approach to RNA quantification.