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Total reactions
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96 | 384 | |
RNA and plate multiplexing format
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96 | 384 | |
Barcoded oligo-dT plates included | 1 | 1 | |
UDI pairs included
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4 | 4 | |
Documentation |
Cat #10881
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Total reactions
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RNA multiplexing format
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96 | |||
UDI pairs included
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4 | |||
Cat #10891
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Total reactions
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RNA multiplexing format
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384 | |||
UDI pairs included
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4 | |||
Benefits
The generated 3' mRNA-seq data is ideally suited for differential gene expression analysis.
High sensitivity for low-input RNA
From as low as 1ng/well.
Bulk RNA sequencing at scale
Perform up-to 384 RNA-seq library preparations in one single tube.
One-day
lab
workflow
Convenient and short protocol from samples to sequencing-ready libraries in one day.
Experimental workflow at a glance

High Sensitivity BRB-seq or standard BRB-seq?
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Selection guide
How to identify the best-performing BRB-seq method for your project.Table 1. Recommended BRB-seq method depending on the RNA input per well
and the number of samples to be pooled.
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Performance
Comparison of library complexity between BRB-seq and HS BRB-seq at the same sequencing depth.Figure 1. Number of detected genes between standard BRB-seq and
High Sensitivity BRB-seq at different RNA inputs per sample.
96 samples were pooled together and sequenced at 2M reads/sample.
To note: all replicates were prepared from the same RNA sample.
Product Specifications
Not ready to use our kits?
No problem, send us your samples and we will generate the data for you! Thanks to BRB-seq and DRUG-seq our service is the most cost-efficient and rapid solution on the market.
