Single-cell FLASH-seq service
This service enables full-length mRNA transcript coverage even for low-abundance genes, empowering researchers to explore differential gene expression, detect alternative splicing, and analyze isoform diversity.
This service enables full-length mRNA transcript coverage even for low-abundance genes, empowering researchers to explore differential gene expression, detect alternative splicing, and analyze isoform diversity.
From differential gene expression to splicing variants and isoform detection.
From samples to data in as little as four weeks.
Step 1
The wells of the plate(s) contain the lysis buffer.
Step 2
Step 3
To preserve sample quality, plates must be placed between dry ice—not just on top. Inadequate cooling may compromise RNA integrity!
Step 4
2 days
Step 5
(Fragment analyzer)
1 week
Step 6
1 week
Step 7
Step 8
The number of detected genes in HEK 293T cells processed with different protocols. Reads were downsampled to 500,000 raw reads.
Number of genes detected in human PBMCs, processed with different protocols, and the number of reads downsampled to 125,000 raw reads.
Gene body coverage shows a uniform read distribution across the entire gene body for the FLASH-seq protocol.
The number of genes detected in HEK 293T cells using different RNA inputs (from 2.5 pg to 250 pg) at different sequencing depths.
We have significantly enhanced the original FLASH-seq method to offer a streamlined workflow and superior data output. This plate-based technology (available in 96- and 384-well formats) features a novel, non-toxic tagmentation buffer and delivers ultra-sensitive gene detection, capturing up to two times more genes compared to other commercially available solutions.
The MERCURIUS™ FLASH-seq protocol is fully compatible with whole FACS-sorted cells.
We do not recommend very large cells, such as cardiomyocytes, as they are not compatible with the FACS sorting step.
We require the cells to be directly FACS-sorted in the dedicated well plates. The 96- and 384-plates contain the lysis buffer. It is important for the user to sort the cells in the middle of the well. Please refer to the Sample Submission Guidelines for more details.
Please note! To preserve sample quality during shipping, plates must be placed between dry ice—not just on top. Inadequate cooling may compromise RNA integrity!
Explore the latest, relevant publications in the industry to learn more about our technologies.
Experience ultra-sensitive and full-length mRNA library prep kit for single-cell sequencing.
Book a one-on-one call with one of our RNA experts to discover how we can assist your next project.