![]() |
![]() |
![]() |
![]() |
![]() |
![]() |
|
---|---|---|---|---|---|---|
Total reactions
|
96 | 384 | 384 | 1'536 | 6'144 | 36'864 |
RNA multiplexing format
|
96 | 96 | 384 | 384 | 384 | 384 |
UDI pairs included
|
4 | 4 | 4 | 4 | 4 | 4 |
Data analysis | ||||||
Manual |
Benefits
The MERCURIUS™ Extraction-free DRUG-seq kits contain all the oligos and enzymes needed to go from 2D cell cultures to sequencing-ready DNA libraries.
Ideal for screening projects
More samples, more replicates. Robust results, significant discoveries.
Streamlined data pre-processing
Demultiplex and align your DRUG-seq data with our easy-to-use cloud-based platform.
No need for prior RNA extraction
An optimized lysis buffer for complete lysis and efficient reverse transcription.
Improved DRUG-seq protocol
Without pre-amplification, leading to higher mapping and gene detection rates.
One-day lab workflow
Convenient and short protocol from samples to sequencing-ready libraries in one day.
Experimental workflow at a glance

Performance
Detection of 12'000+ genes at 1.5 million reads per sample across 384 samples

Distribution of the number of detected genes across...
Detection of 12'000+ genes at 1.5 million reads per sample across 384 samples

Distribution of the number of detected genes across 384 samples prepared with the MERCURIUS™ DRUG-seq library preparation kit. The library was sequenced at an average of 1.5 million reads per sample on an Illumina NovaSeq 6000.
Product Specifications
FAQs
-
Each BRB-seq kit contains reagents (including four pairs of Unique Dual Indexing adapters) sufficient for the complete library preparation process for four different BRB-seq pools.
To note, the total number of RNA samples that can be processed with one kit does not exceed the kit specifications; for instance, a 96-samples kit can be used to prepare up-to 96 samples distributed across up-to four different libraries.
-
The recommended range of input material is in the range of 5’000-50’000 cells.
-
The only difference between BRB-seq and standard RNA-seq data analysis is the demultiplexing step, which is used to assign sequencing reads to their sample of origin based on the BRB-seq barcode sequence.
For a thorough description of BRB-seq data processing, please refer to the BRB-seq kit user guide. In order to facilate as much as possible BRB-seq data analysis, we have also created a dedicate pipeline which can be found in our “SOFTWARE” page.
Speak with our RNA sequencing experts
Book a one-on-one call with one of our RNA experts to discover how we can assist your next project.