Ready for RNA Library Prep without compromise?
- Struggling with degraded RNA in your RNA-Seq workflow?
- Is your RNA library prep producing inconsistent or low-complexity libraries?
- Watching RNA sequencing costs rise due to failed runs?
Get truCOVERed.
truCOVER® Total RNA Library Prep Kits are built to dominate the toughest RNA challenges, especially degraded RNA and FFPE samples, while supporting RNA-seq workflows with speed, precision, and confidence at scale.
REQUEST A TRIAL KIT
Stop accepting tradeoffs in your RNA library prep workflow.
With truCOVER Total RNA Library Prep Kits, you can:
- Detect gene fusions with confidence across standard RNA-seq analysis workflows
- Generate superior, strand specific RNA sequencing libraries with uniform whole transcriptome coverage and minimal duplication
- Harness Adaptive Focused Acoustics® (AFA®) Technology for RNA library preparation with precise, reproducible fragmentation and controlled insert size
- Recover more from less: Optimized for 10–500 ng input and degraded RNA (DV200 ≥30%), including FFPE and low-input applications
- Reduce hands on time by up to 40% with a streamlined, automation ready RNA-seq workflow
- Capture high proportion of exonic reads (~40%), giving high value data for differential gene expression
- Drive rRNA down to <1% of reads, maximizing usable sequencing data and lowering cost per sample
An Optimized RNA Library Prep Workflow for Degraded and Low-Input RNA
From Complex Samples to Clean Data – Better. Faster. Easier.
truCOVER Total RNA Library Prep Kits eliminate workflow variability in your RNA-seq workflow, reduces RNA sequencing waste, and empowers your lab to move from troubleshooting to throughput.
Let’s Optimize Your RNA-seq Workflow
Tell us about your sample type, input amount, and sequencing goals.
Our experts will provide tailored guidance to optimize your RNA library prep and maximize your RNA-seq performance.
It’s time to stop adapting to your samples — and start controlling them.
By utilizing a single-enzyme, single-incubation step for cDNA synthesis and optimizing magnetic bead clean-ups, the protocol reduces workflow time to approximately 4 hours.