truCOVER® Total RNA Library Prep Kits from Covaris LLC

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truCOVER® Total RNA Library Prep Kits

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Description

Overcome the challenges with processing degraded RNA.

High-Performance RNA Library Prep for Challenging Samples
Covaris truCOVER® Total RNA Library Prep is built to dominate the toughest and most complex RNA challenges. From pristine samples to severely degraded FFPE, truCOVER Total RNA Library Prep delivers robust, reliable, powerful, and strand-specific libraries with uncompromising precision, faster than ever before.

Driven by class-leading Adaptive Focused Acoustics® (AFA®) Technology, truCOVER Total RNA Library Prep maximizes RNA recovery, enforces precise and reproducible fragmentation, and significantly cuts down on workflow complexity, while reducing total working time, total number of steps, and overall sequencing costs.

This isn’t incremental improvement. It’s a workflow upgrade. If your lab demands confidence in gene fusion detection, low-input performance with solid reproducibility; this is your solution.

Features:
  • Confident fusion detection: Detect gene fusions and alternative splicing events at lower sequencing depth, because real discoveries can’t wait.
  • Consistent performance with challenging samples: Handle degraded FFPE with confidence; with DV200 values down to 30% without sacrificing quality. Optimize your FFPE sample's extraction-to-sequencing workflow by pairing with Covaris truXTRAC® FFPE Kits.
  • Maximum recovery, minimum waste: Extract powerful libraries from as little as 10 ng up to 500 ng of RNA input.
  • Speed without sacrifice: Complete library prep in nearly 4 hours. Cut hands-on time by up to 40% compared to traditional methods. Automation-ready. Lab-efficient. Deadline-proof.
  • Ultra-clean transcriptomes: rRNA depletion so efficient it drives cytoplasmic and mitochondrial rRNA reads below 1%, unlocking clearer biology and deeper insight.
  • Precision that repeats: AFA-driven consistency ensures reproducible results across runs, operators, and sample types.
  • Consistently higher proportion of exonic reads:30-40% - Maximizes high-value data for differential gene expression (DGE).
  • Better data, bigger ROI: Higher-quality data in less time means smarter sequencing spend and stronger downstream outcomes.