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xGen™ Broad-Range RNA Library Preparation Kit

Comprehensive data from a wide range of RNA inputs

Build stranded RNA-seq libraries from first-strand cDNA with broad input flexibility for limited, variable, or precious RNA samples. Pair with the xGen mRNA Enrichment Module to support mRNA-focused gene expression analysis within a connected transcriptomics workflow.

xGen NGS—made for broad range RNA library preparation.

Ordering

  • Broad input flexibility: Supports a wide range of sample types and inputs, from 10 ng to 1 µg total RNA or 100 pg to 100 ng mRNA, making it well suited for limited, variable, or precious RNA samples.
  • Comprehensive transcriptomic insight: Generates stranded RNA-seq libraries that support strong mapping performance, gene detection, and transcript coverage for whole transcriptome and gene expression studies.
  • Simplified library construction: Uses Adaptase™ technology to build libraries from first-strand cDNA without second-strand cDNA synthesis and degradation, helping reduce workflow complexity.
  • More efficient sequencing focus: Available with the xGen mRNA Enrichment Module to enrich poly(A)-tailed transcripts before library prep, helping direct sequencing reads toward mRNA transcripts most relevant to gene expression analysis.
  • Consistent library performance: Produces consistent libraries with minimal adapter dimers across supported inputs, eliminating the need for adapter titration.
  • Scalable study support: Offers broad indexing options, including UDI and CDI primer pairs with or without Normalase™ technology, to support multiplexing and high-throughput RNA-seq studies.
  • Connected workflow compatibility: Can be combined with xGen hybridization capture reagents when deeper targeted transcript, gene, or pathway analysis is needed.
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Product details

The xGen Broad-Range RNA Library Prep Kit helps researchers build stranded RNA-seq libraries from limited, variable, or precious RNA samples while maintaining a streamlined workflow from first-strand cDNA to sequencing-ready libraries. The kit supports a broad range of inputs, including 10 ng to 1 µg total RNA or 100 pg to 100 ng mRNA, making it a flexible option for transcriptomics studies where sample quantity or quality may vary.

The kit can be paired with the xGen mRNA Enrichment Module to enrich poly(A)-tailed transcripts before library prep, helping focus sequencing reads on mRNA transcripts most relevant to gene expression analysis. It is also compatible with downstream xGen hybridization capture reagents when researchers need to extend from broad transcriptome profiling to targeted RNA sequencing.

Figure 1. xGen Broad-Range Library Prep workflow: After RNA fragmentation, the reverse transcriptase step uses random primers to generate the first-strand cDNA. Next, Adaptase technology simultaneously performs tailing and ligation to incorporate the R2 Stubby Adapter to the 3’ ends of the cDNA molecules. The extension step produces a dsDNA duplex, while ligation adds the R1 Stubby Adapter to the 3’ ends of the primer-extended cDNA molecules. Finally, indexing PCR increases library yield, incorporates single or dual indexes, and results in full-length adapters at the ends of each molecule. In addition, bead-cleanup steps are needed after extension, ligation, and final indexing PCR steps. 

The workflow uses proprietary Adaptase™ technology, which adds a single-stranded R2 Stubby Adapter to the 3’ end of the first-strand cDNA product. This enables stranded RNA library construction without second-strand cDNA synthesis and degradation or template-switching methods, helping reduce workflow complexity while supporting comprehensive transcript coverage and high-quality NGS data.

For scalable studies, the kit supports a range of indexing strategies, including combinatorial dual indexing for up to 96 combinations and unique dual indexing for up to 1536 unique dual indices, with options compatible with Normalase™ technology.

Table 1. xGen Broad-Range RNA Library Prep Kit specifications.

Feature Specification Benefit
Input quantity 10 ng to 1 µg total RNA
100 pg to 100 ng mRNA
Supports a wide input range
Consistent library output
RNA types supported Poly(A)-enriched mRNA
Ribo-depleted RNA
Total RNA
Supports most RNA applications
Technology Adaptase tailing and ligation of 1st strand cDNA No 2nd strand cDNA
No adapter titration
Fewer dimers and duplicates detected in internal research studies (Figure 2)
Maintains strandedness (≥97%)
Higher mapping, transcript detection
Workflow time* 4.5 hours Less hands-on time
Kit reaction sizes 16, 96, and 4x96 Evaluation and adoption
Components provided Fragmentation module
RT module
Library prep
Polymerase
Complete solution for processing total, enriched, or depleted RNA from transcript to library
Indexing options Combinatorial dual
Unique dual
Normalase compatible
Flexible for different sequencers, workflows, and applications
Multiplexing capability Up to 1536 libraries Save sequencing costs
Automation Compatible with liquid handlers
Custom packaging available
Supports high-throughput applications

*Workflow time is based upon incubation times and expected times for hands-on-steps. Actual workflow time may vary depending on individual factors in your laboratory.

Product data

{Workflow time chart compared to competitor K, N, and I - Updated should show NEB approximately same turn but more steps.}

The xGen mRNA Enrichment module has two less washes and reduces binding time by 10 minutes which provides a 15-minute faster workflow compared to Supplier N.

Reduced dimer formation means no adapter titration

Adaptase technology results in minimal adapter dimers, which means no need for adapter titration (Figure 2). Compared to leading RNA library kits, which can produce libraries with >10% adapter dimers and require adapter titration steps, the xGen Broad-Range RNA Library Prep Kit produces <1% adapter dimers and maintains ligation efficiency at all supported input levels.

Figure 2. Comparison of kits. Libraries were prepared using two different kits with the same quantity of input material (n = 1 per input quantity) and subjected to the same number of PCR cycles according to the xGen Broad-Range protocol recommendations during library amplification. Representative library sizes, yields, and BioanalyzerTM (Agilent) traces illustrate typical libraries generated from the same input series of poly(A)-enriched Universal Human Reference (UHR) RNA (Agilent 740000) or human brain mRNA (Takara 636102), when processed by either the xGen Broad-Range RNA Library Prep Kit (left panel) or an RNA library kit from an alternate supplier (right panel). The arrows indicate adapter dimers that were generated during library preparation.

High mapping and transcript identification with lower duplication rates

Figure 3. Comparison of data obtained using different suppliers’ kits. Universal Human Reference (UHR) Total RNA (Agilent 740000) was enriched using the NEBNext® poly(A) mRNA Magnetic Isolation Module (NEB E7490), before being processed by the xGen Broad-Range RNA Library Prep Kit and other supplier kits K and N. For each kit evaluated, libraries were prepared at 10, 100 and 500 ng input, where n = 1 sample per input quantity. PCR amplification of each library was performed as follows: 10 cycles for 500 ng inputs, 12 cycles for 100 ng inputs, and 16 cycles for 10 ng inputs. Libraries were sequenced on a MiniSeqTM with 2x75 bp paired-end reads. Fastq files were downsampled to 2.2 million reads before analysis using STAR (mapping rate), RNASeqC (genes/transcripts detected), or Picard (duplication rate). The xGen Broad-Range RNA Library Prep Kit has high mapping percentage, detects more genes and transcripts, and has fewer duplicates.

Figure 4: Sequencing metric comparison (A) The xGen mRNA Enrichment Module maximizes usable sequencing data delivering higher library yields and cleaner reads with less residual rRNA than Supplier N, while preserving strand specificity. The result is more high-quality, cost-efficient data from every sample. (B) Comprehensive transcriptome coverage you can trust. The xGen mRNA Enrichment Module delivers strong mapping rates and reliably detects a broad range of genes and transcripts so you capture the biology that matters, with less wasted sequencing.

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Frequently asked questions

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