Ion Total RNA-Seq Kit v2
This product is no longer recommended for small RNA applications. Please contact your Field Applications Specialist or Technical Support for additional information.
Ion Total RNA-Seq Kit v2
Ion Torrent™

Ion Total RNA-Seq Kit v2

The Ion Total RNA-Seq Kit v2 includes the reagents needed to prepare representative cDNA libraries for strand-specific RNA sequencing onRead more
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Catalog NumberNo. of Reactions
447978948 Reactions
447593612 Reactions
Catalog number 4479789
Price (USD)
8,020.00
Each
-
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No. of Reactions:
48 Reactions
Price (USD)
8,020.00
Each
Add to cart
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The Ion Total RNA-Seq Kit v2 includes the reagents needed to prepare representative cDNA libraries for strand-specific RNA sequencing on the Ion GeneStudio S5, Ion Proton, or the Ion Personal Genome Machine (PGM) systems. The Ion GeneStudio S5 and Ion Proton systems are ideally suited for sequencing the whole transcriptome (ribosomal RNA depleted or polyA), while the Ion GeneStudio S5 and Ion PGM systems are suitable for viral and bacterial transcriptomes. Version 2 of the Ion Total RNA-Seq Kit is an improvement over the first generation kit. Magnetic bead-based purification replaces all of the filter cleanup steps and the total reaction time has been reduced to 6 hours.

Additional Features of the New Ion Total RNA-Seq Kit v2:

• Greater accuracy—SuperScript VILO and Platinum PCR SuperMix High Fidelity added for highest template fidelity
• Barcode compatible—works with Ion Xpress RNA-Seq Barcode 01-16 Kit for multiplexing
• Automation friendly—magnetic bead-based purification simplifies automation of library construction

As with the previous kit, the Ion Total RNA-Seq Kit v2:

• Preserves strand information—all mapped reads are aligned in the direction of transcription relative to the chromosomal strand
• Allows you to analyze different types of RNA—supports rRNA depleted total RNA, and poly(A) RNA

The Ion Total RNA-Seq Kit v2 is designed to make cDNA library preparation fast and flexible. It can be used to generate a representative cDNA library, flanked by specific sequences necessary for sequencing, from any type of RNA sample.

Designed as a complete solution with a common workflow, the Ion Total RNA-Seq Kit v2 combines optimized reagents and protocols for discovery of coding RNA, noncoding RNA, and alternative splice variants.

Whole transcriptome analysis
The whole transcriptome protocol enables construction of strand-specific libraries in approximately 5 hours. Starting with as little as 100 ng of total RNA, construct a library from 1 ng of poly(A) RNA or 25 ng of rRNA-depleted RNA following the RNA enrichment and library generation protocols provided in the manual. Because the libraries are not limited to cDNA derived only from poly(A) RNA, Ion Total RNA-Seq Kit libraries support a more thorough investigation of transcriptome complexity, capable of characterizing known and undocumented transcripts, including alternative splice variants, fusion transcripts, and SNPs.

Preserve strand information
Unlike methods that ligate adapters to double-stranded cDNA, the Ion Total RNA-Seq Kit v2 utilizes proprietary Ambion technology to attach the adapters in a directional manner that preserves strand information in the resulting libraries. In addition, both the 3' and 5' adapters are attached simultaneously, reducing ligation and clean-up steps.

Preserving strand orientation during library construction helps enable more accurate determination of the structure and expression level of transcripts, and can aid in the discovery of novel transcription regions from both the positive and negative genomic strands.

The Ion Total RNA-Seq Kit v2 is designed to create RNA libraries from up to 48 samples for whole transcriptome sequencing on the Ion GeneStudio S5, Ion Proton, or Ion PGM systems.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Sample TypeRNA
For Use With (Equipment)Ion GeneStudio™ S5, Ion PGM™, Ion Proton™ Systems
No. of Reactions48 Reactions
LibrariescDNA Library
Product LineIon Torrent™
Quantity48 reactions
Sequencing TypeTranscriptome Sequencing
Starting Material AmountFor RNA (rRNA-depleted): 1-100 ng mRNA
For whole transcriptome: ≥100 ng total RNA
Workflow StepNGS Library Generation
Unit SizeEach
Contents & Storage
Store at -20°C:
1 tube, 10X RT Buffer 48 reactions
1 tube, 2.5 mM dNTP Mix 48 reactions
1 tube, Platinum HiFi MasterMix 48 reactions
1 tube, 10x Superscript Enzyme Mix 48 reactions
1 tube, Ion 3'-PCR-primer v2 48 reactions
1 tube, Ion 5'-PCR-primer v2 48 reactions
1 tube, Ion 5'-PCR-primer v2 48 reactions
1 tube, Ion RT Primer v2 48 reactions
1 tube, Ion Adaptor Mix v2 48 reactions

Store at 4°C:
1 bottle, Binding Soluntion Concentrated 48 reactions
1 bottle, Wash Soln Concentrated 48 reactions
1 bottle, Nucleic Acid Binding Beads 48 reactions
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Frequently asked questions (FAQs)

Generally, a successful Ion RNA-Seq library will be within the recommended size range for sequencing on the Ion PGM or Proton systems and the sequencing data will have a high (or expected) percentage of on-target reads.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

Please visit the Transcriptome Sequencing by Ion Torrent Sequencing page (https://www.thermofisher.com/us/en/home/life-science/sequencing/rna-sequencing/transcriptome-sequencing/transcriptome-sequencing-ion-torrent-next-generation-sequencing.html) for information on RNA-Seq data analysis using Torrent Suite Software, or 3rd party software providers.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

The GGCCAAGGCG sequence is part of the RNA library adapter sequence. This sequence can be automatically trimmed by the software by selecting the “RNA_Barcode_None” option under the Barcodes menu. The run can be reanalyzed with the correct barcode settings to trim the adapter sequence. In the future, the “RNA_Barcode_None” option should be selected in the run plan or selected on the instrument prior to starting the sequencing run.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

RNA-Seq relies on a random sampling strategy in which most sequencing reads will identify abundant transcripts with an increasing number of reads needed to identify lower abundant transcripts and/or low levels of gene expression. While depletion and purification strategies are available from Thermo Fisher Scientific to remove unwanted abundant transcripts and increase sequencing power, transcript detection sensitivity is a function of mapped reads. Accordingly, the complexity of the genome under investigation should be taken into account when planning an RNA-Seq experiment. Applications that require a small number of reads, such as low multiplexed gene expression, can be performed on the Ion 318 Chip Using the PGM platform whereas, human/mammalian transcriptomes and highy-multiplexed gene expression profiling should be performed on the GeneStudio platforms, using the higher throughput chips. For more information, please see the Transcriptome Sequencing by Ion Torrent Sequencing page (https://www.thermofisher.com/us/en/home/life-science/sequencing/rna-sequencing/transcriptome-sequencing/transcriptome-sequencing-ion-torrent-next-generation-sequencing.html).

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

Another method is chemical fragmentation (not part of the protocol), which is useful for quantifying exon levels, novel splicing identification, and fusion gene discovery, and provides more uniform coverage for viral and bacterial transcripts. Chemical fragmentation is more randomized than RNase III fragmentation, but can be difficult to optimize. Chemically fragmented RNA fragments require repair with T4 polynucleotide kinase (not included in kit) before proceeding into ligation.

Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.

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