MERCURIUS™

Total Plant BRB-seq Kits
for cost-effective plant
RNA-seq

Streamlined total RNA library preparation for purified plant RNA, combining plant-focused rRNA depletion with early multiplexing to make whole-transcriptome profiling more accessible across plant research, crop science, and agrochemical R&D.

Compatible with Illumina® and AVITI™ sequencers.

Multiplexed
total RNA

Full-length transcript coverage

Plant-focused rRNA depletion

One-day library prep workflow

Product Overview

MERCURIUS™ Total Plant BRB-seq is a cost-effective total RNA-seq library preparation kit for purified plant RNA. Built on Alithea Genomics’ BRB-seq technology, it combines plant-focused rRNA depletion with early sample barcoding and multiplexing, enabling up to 96 samples to be pooled into a single tube early in the workflow.

Designed for plant transcriptomics studies, Total Plant BRB-seq provides full-length coding and non-coding transcript coverage for gene and isoform quantification, supporting applications such as crop stress response, pathogen surveillance, plant protection product testing, herbicide toxicity studies, biomarker discovery, and plant genome annotation.

The kit is compatible with Illumina® and AVITI™ sequencers and supports RNA inputs from 100 pg to 100 ng per well.

preps in a single tube
Up to 96
detected genes at
2M reads/sample
20,000 +
library prep workflow
Down to 1 day

Applications

MERCURIUS™ Total Plant BRB-seq is designed for plant transcriptomics studies where researchers need scalable, cost-effective total RNA-seq with full-length transcript coverage.

  • Crop stress and disease response
    Profile transcriptome-wide responses to drought, heat, nutrient stress, infection, or other biological and environmental pressures.
  • Pathogen surveillance and viral detection
    Support plant health monitoring and disease research by capturing broader RNA signatures from purified plant RNA samples.
  • Plant protection product testing
    Study how crops respond to agrochemical treatments, including plant protection products, herbicides, and other compounds used in agricultural R&D.
  • Biomarker discovery
    Identify gene expression signatures linked to crop stress, disease resistance, treatment response, or desirable plant traits.
  • Plant genome annotation
    Generate full-length transcript information to support transcript discovery, isoform analysis, and improved genome annotation.
  • Crop and seed research
    Compare gene expression across genotypes, varieties, tissues, treatments, or timepoints in breeding and crop improvement studies.

Total Plant BRB-seq has superior exonic read enrichment compared to BRB-seq in A. thaliana.

Stacked bar plots showing the distribution of mapped reads for Total Plant BRB-seq and BRB-seq in A. thaliana. A higher proportion of Total Plant BRB-seq reads map to coding (CDS) as expected for full-length methods.

Total Plant BRB-seq detects similar numbers of genes to BRB-seq in A. thaliana across sequencing depths.

Saturation curves comparing Total Plant BRB-seq and BRB-seq gene detection across a range of downsampled read depths in A. thaliana. Total Plant BRB-seq detects a similar number of genes to BRB-seq across all downsampled sequencing depths, with both methods detecting around 18,000 genes at 1M reads per sample. The full-length information is especially beneficial for less well-annotated genomes, where 3’ UTR may not be complete.   

Total Plant BRB-seq achieves broad, full-length transcript coverage in melon (C. melo).

Normalized 5’ to 3’ read coverage across the transcript body for Total Plant BRB-seq in C. melo. Reads are distributed broadly across the full transcript length, confirming that Total Plant BRB-seq captures full-length transcript information rather than the 3′-bias associated with standard poly-A enrichment methods like BRB-seq.

Total Plant BRB-seq detects almost 15,000 genes in melon (C. melo) at 1M reads per sample.

Gene detection saturation curve for Total Plant BRB-seq in C. melo, with detected genes as a function of downsampled read depth. Gene detection increases rapidly below 500K reads per sample, demonstrating broad coverage of the C. melo transcriptome.

Total Plant BRB-seq achieves broad, full-length transcript coverage in tomato (S. lycopersicum).

Normalized 5’ to 3’ read coverage across the transcript body for Total Plant BRB-seq in S. lycopersicum. Reads are distributed broadly across the full transcript length, confirming that Total Plant BRB-seq captures full-length transcript information rather than the 3′-bias associated with standard poly-A enrichment methods like BRB-seq.

Total Plant BRB-seq detects over 15,000 genes in tomato (S. lycopersicum) at 1M reads per sample.

Gene detection saturation curve for Total Plant BRB-seq in S. lycopersicum, with detected genes shown as a function of downsampled read depth. Gene detection increases rapidly below 500K reads per sample and plateaus near saturation of approximately 16,500 genes at 4.5M reads.

Product documentation

Barcode files

User guide

Publications

2026
Larissa Carvalho Costa, Christopher Gottschalk, Davis M. Upchurch, Oscar P. Hurtado-Gonzales, Ben N. Mansfeld, Alan Yocca, Lauren Whitt, Cheryl Vann, Gennaro Fazio
2024
Stéphanie Boder‐Pasche, Mustafa Demir, Sarah Heub, Manon Garzuel, Réal Ischer, Daniel Migliozzi,  Siegfried Graf, Noa Schmid, H. Baris Atakan, Daria Gudkova, Daniel Alpern,  Riccardo Dainese, Bart Deplancke, Gilles Weder

Application

Full-length and total RNA sequencing

Equipment compatibility

Illumina and AVITI instruments

Species compatibility

Purified RNA from plants

Available formats

96 preps

Shipping conditions

Dry ice

Storage conditions

-20C

Each kit includes 4 Unique Dual Index (UDI) pairs, so you can prepare up to 4 indexed libraries (pools) per kit.

The tested input range is 100 pg to 100 ng total RNA per well. For best results (library complexity + uniformity), aim for 10–100 ng per well, and pool at least 8 wells per library.
Because Total BRB-seq uses early multiplexing, it’s important that RNA quantity and quality are consistent across samples (e.g., RIN > 7, 260/230 > 1.5, and ~±10% input uniformity).

Total BRB-seq is designed for total RNA sequencing (not just mRNA), including coding and non-coding transcripts, and includes an rRNA depletion step prior to library prep.

We recommend 3-5 million reads for gene detection and >10 million reads for isoform and transcript analysis.

Yes, there is one extra step: after standard index demultiplexing, you demultiplex by sample barcodes to generate per-sample gene/transcript count outputs. The workflow supports producing outputs like UMI count matrices, gene count matrices, and a QC report.

Go to the “Resources” section of this page and click on the button to download the barcode files for the product you are using.

Yes. If you are not ready to run kits internally, Alithea can run the workflow and deliver FASTQ files, gene count matrices, and analysis report files.

Ask your question:

Kit name

Catalog number

Total
preps
Barcoded plates
UDI
pairs
Species compatibility

MERCURIUS™ Total Plant BRB-seq library prep kit (96 preps)

#10815
96
1
4
Arabidopsis thaliana, Zea mays, Actuca sativa, Cucumis melon, Spinacia oleracea, Solanum lycopersicum, Citrullus lanatus*

MERCURIUS™ Total Plant BRB-seq library prep kit (4x96 preps)

#11815
384
4
4
Arabidopsis thaliana, Zea mays, Actuca sativa, Cucumis melon, Spinacia oleracea, Solanum lycopersicum, Citrullus lanatus*

* Contact us to inquire about compatibility with other species. 

Accessories

Product

Catalog Number

UDI Pairs

MERCURIUS™ UDI X-Leap Expansion module

#10493
4

MERCURIUS™ Full-Length Post-Pooling Preparation Module (4 libraries)

#10509
-

Ordering tip

Each kit includes 4 UDI pairs. Add the expansion module if you need more unique indexes (total 16 UDI pairs available). 

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