The product previously known as the TruSeq Stranded mRNA Library Prep Kit (Cat. No. RS-122-2101, RS-122-2102, and RS-122-2103) is now called TruSeq Stranded mRNA. The product configuration has changed. In the new configuration, the library preparation and index adapters can be purchased separately. The list of components available for individual purchase can be found in the “Select Product(s)” section.

TruSeq Stranded mRNA

Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information. Read More...
Select Product(s)
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Library Prep

TruSeq® Stranded mRNA Library Prep (48 Samples)

20020594

Price
 
 

TruSeq Stranded mRNA Library Prep (96 Samples)

20020595

Price
 
 

Index Adapters

TruSeq RNA Single Indexes Set A (12 Indexes, 48 Samples)

20020492

Price
 
 

TruSeq RNA Single Indexes Set B (12 Indexes, 48 Samples)

20020493

Price
 
 

TruSeq RNA CD Index Plate (96 Indexes, 96 Samples)

20019792

Price
 
 

IDT for Illumina – TruSeq RNA UD Indexes (24 Indexes, 96 Samples)

20020591

Price
 
 

IDT for Illumina – TruSeq RNA UD Indexes (96 Indexes, 96 Samples)

20022371

Price
 
 
Accessory Products

Illumina Free Adapter Blocking Reagent (12 reactions)

20024144

Price
 
 

Illumina Free Adapter Blocking Reagent (48 reactions)

20024145

Price
 
 

Product Highlights

TruSeq Stranded mRNA offers a streamlined, cost-efficient, and scalable solution for coding transcriptome analysis. It is compatible with a wide range of samples.

Strand Orientation Detection

Get precise measurement of mRNA strand orientation for detection of antisense transcription, enhanced transcript annotation, and increased alignment efficiency. High coverage uniformity enhances the discovery of features such as alternative transcripts, gene fusions, and allele-specific expression.

Cost-Efficient

Stranded information identifies from which of the 2 DNA strands a given RNA transcript was derived. This information provides increased confidence in transcript annotation, particularly for nonhuman samples. Identifying strand origin increases the percentage of reads that align, reducing sequencing costs per sample.

Scalable

The workflow enables robust interrogation of both standard and low-quality samples, and workflows compatible with a wide range of study designs.

Find a list of high-throughput automation vendors with robotic systems compatible with this product

Read a comprehensive assessment of Illumina’s ribosomal RNA depletion protocol

Frequently Purchased Together

Specifications

Project Recommendations

Instrument Recommended Number of Samples Read Length
NextSeq 550 System RNA Profiling: 13–40 samples per run (based on 10 million reads per sample)
Transcriptome Analysis: 5–16 samples per run (based on 25 million reads per sample)
2 x 75 bp
2 x 75 bp
HiSeq 2500 System RNA Profiling: 60–400 samples per run (dual flow cell; based on 10 million reads per sample)
Transcriptome Analysis: 24–160 samples per run (dual flow cell; based on 25 million reads per sample)
2 x 75 bp
2 x 75 bp
NovaSeq 6000 System RNA Profiling (samples per run, dual flow cell): S1: 320, S2:384, S4:768. Limited by index combinations (dual). Based on 10 million reads.
Transcriptome Analysis (samples per run, dual flow cell): S1: 128, S2: 256, S4: 768. Limited by index combinations (dual). Based on 25 million reads. 
≤ 2 × 100 bp
≤ 2 × 100 bp

Product Comparison

TruSeq Stranded mRNA TruSeq RNA Library Prep Kit v2 TruSeq RNA Exome SureCell WTA 3′ Library Prep Kit for the ddSEQ System
Assay Time ~10.5 hours ~10.5 hours ~2 Days 11-12 hours
Content Specifications Captures the coding transcriptome with strand information Captures the coding transcriptome (without strand information) Captures the coding transcriptome/RNA exome Captures the coding transcriptome (3' enriched), with strand-specific information
Description Gives researchers a clear, comprehensive view of the coding transcriptome with precise strand information. A simple, cost-effective research solution for analysis of the coding transcriptome. Gives researchers a clear, comprehensive view of the coding transcriptome with precise strand information and a reduced sample input requirement. Enables single-cell RNA-Seq studies using a droplet generator that isolates ~1200 cells per cartridge, and a simple library prep process.
Hands-On Time ~4.5 hours ~4.5 hours ~11 hours 4-5 hours
Input Quantity 0.1 – 1 ug total RNA or 10 - 100 ng previously isolated mRNA (from species with polyA tails) 0.1 - 1 ug total RNA or 10 - 400 ng previously isolated mRNA (from species with polyA tails) 10 ng total RNA from fresh/frozen samples, or 20 ng total RNA from FFPE samples ~45,000 cells per cartridge (required input)
Mechanism of Action Oligo-dT beads capture polyA tails Oligo-dT beads capture polyA tails Biotinylated capture probes that target coding RNA. Does not require RNA with poly-A tails. Oligo dT capture, single cell
Method mRNA Sequencing mRNA Sequencing Exome Sequencing , mRNA Sequencing mRNA Sequencing
Multiplexing 1–96 Up to 24-plex per lane Up to 24 single, 96 combinatorial (CD) dual 1-24
Specialized Sample Types Not FFPE-Compatible Not FFPE-Compatible FFPE Tissue, Low-Input Samples Not FFPE-Compatible, Single Cells
Species Category Bovine, Human, Mammalian, Mouse, Rat Bovine, Human, Mammalian, Mouse, Rat Human Human, Mouse
Strand Specificity Stranded Non-Stranded Stranded Stranded

Method-Specific Workflow Example

 

Customer Stories

Unraveling Disease Mechanisms With The NextSeq 500 System

Researchers at the Icahn School of Medicine at Mount Sinai are studying mtDNA, piRNA, and TCR repertoire diversity to unlock the secrets of cancer, infertility, and autoimmune disease.

Read More
Precision Immunotherapies Using Tumor-Specific HLA Ligands

RNA-Seq and HLA typing are increasing the power and efficiency of a target discovery platform.

Read More

Supporting Data and Figures

Technical Replicates
Supporting Data and Figures

Figure 2 from TruSeq Stranded mRNA and Total RNA Library Prep Kits Data Sheet, December 2015

Technical replicates of FFPE tissue show high concordance, indicating robust library prep performance. Axes are log2(FPKM). R2 value is shown.

 
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Determine the best library prep kit or array for your needs based on your starting material and method of interest.

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Related Products

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Prepare whole-transcriptome sequencing libraries from blood-derived RNA with an efficient workflow that removes ribosomal RNA and globin mRNA in a single step.


This product and its use are the subject of one or more issued and/or pending U.S. and foreign patent applications owned by Max Planck Gesellschaft, exclusively licensed to New England Biolabs, Inc. and sublicensed to Illumina, Inc. The purchase of this product from Illumina, Inc., its affiliates, or its authorized resellers and distributors conveys to the buyer the non-transferable right to use the purchased amount of the product and components of the product by the buyer (whether the buyer is an academic or for profit entity). The purchase of this product does not convey a license under any claims in the foregoing patents or patent applications direct to producing the product. The buyer cannot sell or otherwise transfer this product or its components to a third party or otherwise use the product for the following COMMERCIAL PURPOSES: (I) use of the product or its components in manufacturing; or (2) use of the product or its components for therapeutic or prophylactic purposes in human or animals.