RNA Library preparation
Revolutionise your RNA research
The RNA library preparation kits offer a range of benefits, including high accuracy, long reads, and fast turnaround times. Every research project is unique, so to cater to different research projects, a range of kits are available. Confidently characterise and quantify full-length RNA transcripts, splice variants, and fusions using short to ultra-long fragment nanopore sequencing. Accurately analyse differential gene expression and transcript usage. Sequence native RNA directly, without amplification or reverse transcription, and identify base modifications.
Browse the full range of library prep solutions
PCR-free protocols to elimate bias
Library for full-length transcripts sequencing
cDNA sequencing
Single-cell sequencing
Base modifications preserved
| Direct RNA | cDNA | |
|---|---|---|
| Direct RNA Sequencing Kit | cDNA-PCR Sequencing Kit | |
| Preparation time | 135 min | ~225 mins + PCR |
| Input recommendation | 300 ng poly(A)+ RNA or 1 μg total RNA | 10 ng poly(A)+ RNA or 500 ng total RNA |
| Fragmentation | Optional | Yes |
| Amplification | No | Yes |
| Barcode options | In development | cDNA-PCR Barcoding Kit (24 plex) |
| Typical output | 20M reads | >100M reads |
| Adaptive sampling | In development | In development |
| Methylation included | Yes | - |
RNA sequencing with nanopore technology
