LoopSeq Transcriptome 3x8-plex Kit Add to Cart
This kit provides a comprehensive isoform survey and accurate relative abundance of every transcript in RNA samples. Single molecule long read data is generated as well as relative abundance using barcode based molecular counting. It also features a multiplex workflow that pools 3 x 8 samples into a single tube with less than 3 hours of hands-on time.
It’s the perfect kit for labs looking to profile every polyA-tailed transcript in their RNA sample.
Compatible with all Illumina instruments*
*HiSeqs, NextSeqs, and NovaSeqs are recommended for per base cost benefits.
Supercharge your research with the power of LoopSeq single-molecule, long-read transcriptome sequencing
Multiplex workflow: Pool all samples into a single tube.
Full-length transcripts: Single-molecule long-read transcript data.
Reduced Error Rate: High resolution long read sequence data at less errors than on PacBio and Oxford Nanopore platforms.
UMI based transcript counting: Barcode based quantification with no PCR bias.
- Liu S. et al. (2020) Targeted Transcriptome Analysis using Synthetic Long Read Sequencing Uncovers Isoform Reprograming in the Progression of Colon Cancer. bioRxiv.