Product Overview
QuantSeq Expression Profiling Library Prep Kits
QuantSeq kits enable cost-efficient sequencing by counting. These kits are an exceptional alternative to standard RNA-Seq and microarrays. Just one fragment per transcript is produced and therefore there is no need for length normalization. This makes data analysis very simple and accurate. By using Lexogen’s 96 i5 x 96 i7 dual indices up to 9,216 samples can be multiplexed in one lane, saving your sequencing space. Moreover, unique 96 i5 x 96 i7 indices help detect and quantify index hopping and minimize mis-assignment. QuantSeq is available for 3’ mRNA-Seq and targeted RNA-Seq.
QuantSeq 3′ mRNA-Seq Library Prep Kit FWD is the best solution for genome-wide gene expression analysis by sequencing towards the poly(A) tail. The kit is available for Illumina and Ion Torrent platforms.
New! QuantSeq-Pool Sample-Barcoded 3′ mRNA-Seq Library Prep Kit for Illumina is the most convenient solution for gene expression profiling for large screening projects. Using early pooling and batch processing it is easily scalable from a few to 36,864 samples.
QuantSeq 3′ mRNA-Seq Library Prep Kit REV for Illumina is designed in a way that NGS reads start directly at the 3’ end of transcripts, enabling detailed 3’ UTR analysis and the study of alternative polyadenylation.
QuantSeq-Flex Targeted RNA-Seq Library Prep Kit V2 is designed to make Illumina compatible libraries from any RNA sample using custom primers. It is open for development by advanced RNA-Seq users based on their custom needs.
New! Up to 384 Unique Dual Indices (UDIs) featuring superior error correction for maximal sequencing data output included in new QuantSeq kits (Cat. No. 113 – 115, 129 – 131).
CORALL RNA-Seq Library Prep Kit
CORALL is Lexogen’s stranded whole transcriptome RNA-Seq library prep kit. CORALL enables streamlined generation of Illumina-compatible libraries within 4.5 hours, featuring seamless integration of Unique Molecular Identifiers (UMIs) and exceptional protocol-inherent strand specificity (>99%). The fragmentation-free protocol uses Lexogen’s proprietary Strand Displacement Stop and Ligation technologies to deliver complete transcript representation, including exact start and end sites.
New! CORALL mRNA-Seq Kits provide a complete solution for mRNA sequencing and include poly(A) selection and library preparation to generate sequencing-ready whole transcriptome mRNA libraries in 5.5 hours. All CORALL mRNA-Seq Kits contain Unique Dual Indices (UDIs) featuring superior error correction for maximal sequencing data output.
CORALL Total RNA-Seq Kits are available with single or dual indexing options and are the ideal choice for Total RNA-Seq library generation after ribo-depletion with Lexogen’s RiboCop rRNA Depletion Kits. For convenience, CORALL Total RNA-Seq Kits are also available as bundled versions with RiboCop rRNA Depletion Kits.
New! Up to 384 Unique Dual Indices (UDIs) featuring superior error correction for maximal sequencing data output included in new CORALL Total RNA-Seq kits with UDIs (Cat. No. 117 – 119, 132 – 134).
New! LUTHOR 3’ mRNA-Seq Library Prep Kit
LUTHOR combines the novel THOR (T7 High-resolution Original RNA) Amplification Technology with a highly efficient library preparation for 3’ mRNA-Seq analysis of one individual cell or ultra-low RNA input. It provides unprecedented sensitivity, reproducibility, and a reduction of systematic errors. This template-switch-, ligation- and fragmentation-free protocol enables RNA-Seq even from challenging individual, singularized cells.
New! TraPR Small RNA Isolation Kit
The TraPR Small RNA Isolation Kit isolates functional, physiologically relevant silencing sRNAs from any organism, tissue, cell type, or bio-fluid. In contrast to previous state-of-the-art methods, this innovative 15-minute single-column workflow neither requires prior knowledge of the sample, nor does it involve tedious gel extraction steps or lengthy immuno-precipitation procedures. TraPR thus enables the extraction of high-quality sRNAs even from challenging or uncharacterized material, leading to highly reproducible sequencing results.
Small RNA-Seq Library Prep Kit
Small RNA-Seq Library Prep Kit provides a protocol for generation of small RNA libraries for Illumina sequencing directly from total RNA or enriched small RNA.
SPLIT RNA Extraction Kit
SPLIT RNA Extraction Kit for extraction of total RNA or small and large RNA fractions free of genomic DNA from any cell type.
New! SPLIT RNA Extraction Kit for Blood for efficient depletion of globin mRNA during the extraction.
Lexogen Indexing Solutions
Lexogen offers single and dual indexing solutions for all needs. Most common solutions are included in all Lexogen’s library prep kits and additional variations are available as Add-on Kits.
New! 384 Unique Dual Indices with superior error correction for maximal sequencing data output.
SLAMseq Metabolic RNA Labeling Kit for RNA-Seq
SLAMseq is a high-sensitivity method for time-resolved measurement of newly synthesized and existing RNA in cultured cells. SLAMseq enables resolution of RNA synthesis and degradation kinetics.
RiboCop rRNA Depletion Kits
RiboCop rRNA Depletion Kits for Human/Mouse/Rat and for Bacteria enable removal of ribosomal RNA from total RNA and are suited for Next Generation Sequencing as well as other demanding RNA analysis applications.
New! RiboCop HMR V2 with improved performance on degraded RNA samples.
New! Now also available for combined rRNA and globin mRNA depletion.
TeloPrime Full-Length cDNA Amplification Kit V2
TeloPrime Full-Length cDNA Amplification Kit V2 generates full-length cDNA from total RNA. It is highly selective for full-length RNA molecules that are both capped and polyadenylated and therefore no cDNA from degraded RNA is being amplified. High-efficiency PCR produces excellent cDNA yields ideal for downstream long-read sequencing applications.
SIRVs (Spike-in RNA Variant Control Mixes)
The SIRVs are a set of transcript variants designed to assess RNA sequencing workflows for their performance in transcriptome analysis in categories such as detection of isoforms, linearity of dose response and sensitivity, and transcript length. This includes the testing of bioinformatic algorithms for their ability to quantify, map, and assemble isoforms. In addition to these validation applications, the SIRVs can function as “fingerprints” to assess concordance of RNA-Seq data sets.
Mix2 RNA-Seq Data Analysis Software
A software tool for the accurate estimation of RNA concentration from RNA-Seq data.
- Precise transcript concentration estimates
- Accurate detection of differential expression
- Exceptional reproducibility across variable conditions
- Fast run-times and small memory footprint
Library Prep Kits Overview
| Kit Selection Criteria | CORALL Total RNA-Seq | QuantSeq | LUTHOR 3′ mRNA-Seq | Small RNA-Seq | TeloPrime full-length cDNA | |||||
| + Poly(A) | + RiboCop | QuantSeq 3′ FWD | QuantSeq 3′ Pool | QuantSeq 3′ REV | QuantSeq-Flex | |||||
| Expression Profiling |  |
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| Whole Transcriptome (full-transcript coverage) | |
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| Alternative Polyadenylation / 3′ UTR isoforms | |
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| Isoform discovery & quantification | |
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| Target-Specific | |
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| RiboSeq (Ribosomal profiling) | |
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| Polysome profiling | |
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| Transcript (re)annotation | |
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3’UTR only |
3’UTR only |
3’UTR only |
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3’UTR only |
sRNA only |
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| de novo assembly | |
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| SLAMseq (Nascent RNA-Seq) | |
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| Small RNA (e.g., miRNA) analysis | |
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| Long non-coding RNA analysis | |
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| rRNA Sequencing | * |
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| Dual indexing compatible | |
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| Automation-Compatible | |
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| UMIs available | included | included | included | |
included | |
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| Data Analysis pipeline available | |
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included | |
included | |
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| Service available | |
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| Spike In control recommendation | SIRV-Set 1/2/3 | SIRV-Set 3 | |
SIRV-Set 3 | |
SIRV-Set 1/2/3 |
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| 8 rxn kit | |
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| 24 rxn kit | |
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| 96 rxn kit | |
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| 2×96 rxn kit | |
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| 384 rxn kit | |
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Legend:
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Optimal Choice |
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Yes |
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Possible, but not evaluated. For more information please contact support@lexogen.com. |
| pA |
Possible only if a poly(A) tail (and a 5′ cap for TeloPrime) is present or with prior poly-adenylation |
| M |
Protocol modifications apply |
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Not possible or not useful |