UDI X-Leap module
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Compatible with the full-length mRNA and total RNA MERCURIUS™ product lines
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4 UDI pairs.
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Flexible dual indexing solutions.
MERCURIUS™
Full-length and total RNA library preparation kits featuring early multiplexing for purified blood RNA - compatible with human samples
RNA-seq library preps with integrated globin depletion.
Compatible with Illumina® and AVITI™ sequencers.
Catalog number | #10720 |
#11720 |
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Total preps
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96 | 384 | ||
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Sample multiplexing and plate format
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96 | 96 | ||
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Barcoded oligo-dT plates included
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1 | 4 | ||
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UDI pairs included
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4 | 4 | ||
| Globin blockers | included | included | ||
| Documentation | ||||
| Cat ##10720 | ||||
|---|---|---|---|---|
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Total reactions
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96 | |||
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RNA multiplexing format
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96 | |||
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UDI pairs included
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4 | |||
| Globin blockers | included | |||
| Cat ##11720 | ||||
|---|---|---|---|---|
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Total reactions
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384 | |||
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RNA multiplexing format
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96 | |||
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UDI pairs included
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4 | |||
| Globin blockers | included | |||
Compatible with the full-length mRNA and total RNA MERCURIUS™ product lines
4 UDI pairs.
Flexible dual indexing solutions.
The MERCURIUS™ Total Blood BRB-seq library preparation kits for Illumina® and AVITI™ contain all the oligos and enzymes needed to go from purified blood RNA to sequencing-ready libraries.

1. Detection of 17'000+ genes per sample across 96 samples


Distribution of the number of detected genes across 96 samples prepared with the MERCURIUS™ Blood BRB-seq library preparation kit and the MERCURIUS™ Total Blood BRB-seq. The libraries were sequenced at the same sequencing depth.
2. Total Blood BRB-seq provides effective and high-throughput inline depletion of globin genes

(Top) The distribution of reads mapped to non-globin and globin genes per sample for one 96 sample Total Blood BRB-seq library without globin depletion. An average of approximately one-third of reads mapped to globin genes. (Bottom) The distribution of reads mapped to non-globin and globin genes per sample for the same 96 samples in one Total Blood BRB-seq library treated with globin depletion. The reads associated with globin genes are drastically reduced, with more reads mapped to non-globin genes.
3. Gene saturation analysis comparing the Blood BRB-seq and the Total Blood BRB-seq library preparation workflows

The plot shows the number of detected genes as a function of sequencing depth for both MERCURIUS™ Blood BRB-seq library preparation kit and the MERCURIUS™ Total Blood BRB-seq.
4. Total Blood BRB-seq exhibits reads distribution across the transcript’s entire length

The gene body coverage shows a consistent and uniform read distribution across the entire gene body for the Total Blood BRB-seq protocol, while the Blood BRB-seq protocol shows a significant 3' bias due to its poly-A selection methodology.
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For (application) |
Total RNA sequencing |
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For use with (equipment) |
Illumina and AVITI NGS instruments |
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Species compatibility |
Human |
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Available formats |
96 preps |
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Shipping conditions |
Dry ice |
|
Storage conditions |
-20C |

1. Detection of 17'000+ genes per sample across 96 samples


Distribution of the number of detected genes across 96 samples prepared with the MERCURIUS™ Blood BRB-seq library preparation kit and the MERCURIUS™ Total Blood BRB-seq. The libraries were sequenced at the same sequencing depth.
2. Total Blood BRB-seq provides effective and high-throughput inline depletion of globin genes

(Top) The distribution of reads mapped to non-globin and globin genes per sample for one 96 sample Total Blood BRB-seq library without globin depletion. An average of approximately one-third of reads mapped to globin genes. (Bottom) The distribution of reads mapped to non-globin and globin genes per sample for the same 96 samples in one Total Blood BRB-seq library treated with globin depletion. The reads associated with globin genes are drastically reduced, with more reads mapped to non-globin genes.
3. Gene saturation analysis comparing the Blood BRB-seq and the Total Blood BRB-seq library preparation workflows

The plot shows the number of detected genes as a function of sequencing depth for both MERCURIUS™ Blood BRB-seq library preparation kit and the MERCURIUS™ Total Blood BRB-seq.
4. Total Blood BRB-seq exhibits reads distribution across the transcript’s entire length

The gene body coverage shows a consistent and uniform read distribution across the entire gene body for the Total Blood BRB-seq protocol, while the Blood BRB-seq protocol shows a significant 3' bias due to its poly-A selection methodology.
|
For (application) |
Total RNA sequencing |
|
For use with (equipment) |
Illumina and AVITI NGS instruments |
|
Species compatibility |
Human |
|
Available formats |
96 preps |
|
Shipping conditions |
Dry ice |
|
Storage conditions |
-20C |
Each Total Blood 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-sample kit can be used to prepare up to 96 samples distributed across up-to four different libraries.
No, the Total Blood BRB-seq workflow is only dedicated to human blood samples.
The recommended range of RNA amount for each sample is of 10ng-100ng.
The minimum recommended RIN number is 7 and the A260/280 ratio (Nanodrop) should be A260/280 >1.5
The only difference betweenTotal Blood 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 barcode sequence.
For a thorough description of Total Blood BRB-seq data processing, please refer to the kit user guide.
The recommend sequencing depth for the Total Blood BRB-seq libraries is between 2-10 M reads per sample, which is typically enough to detect the vast majority of expressed genes.
The barcode set for your kit is conveniently located on the kit label. Please refer to the label for accurate identification.
For optimal compatibility, ensure that you use the appropriate plate format (e.g., for kits designed for 96 reactions, the 96 well-plate format should be used). This ensures accurate and efficient processing of your samples. If you have any further questions or concerns, please contact our support team for assistance by email or using our live chat tool.
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