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Nurture Growth,
Harvest Discoveries

Unveil the Complete Plant
Transcriptome with RiboCop

RiboCop for Plants

Plant total RNA is comprised of large amounts of undesired ribosomal RNA (rRNA) which accounts for up to ~97 % of all transcripts. Lexogen’s RiboCop rRNA Depletion Kits for Plants remove undesired cytoplasmic (5.8S, 18S and 25S), mitochondrial (5S, 18S and 26S) and plastid (4.5S, 5S, 16S and 23S) rRNA from intact as well as degraded input RNA. Ribo-depletion affords an unbiased view of the transcriptome, including non-coding and non-polyadenylated RNA species.

RiboCop for Plants is ideally suited for Next Generation Sequencing (NGS) approaches in combination with CORALL RNA-Seq V2 Library Preparation Kits. RiboCop Kits are also compatible with other random primed total RNA library prep kits.

Performance

Ribosomal RNA was depleted from Arabidopsis thaliana total RNA using RiboCop for Plants over a wide range of input amounts (1 ng to 1 µg). RiboCop for Plants efficiently reduces rRNA reads for all input amounts (Fig. 1).

Figure 1 | RiboCop rRNA Depletion for Plants efficiently removes rRNA across a wide range of input amounts. NGS libraries were prepared using Lexogen’s CORALL RNA-Seq V2 Library Prep Kit. Successful depletion was monitored by NGS sequencing (NextSeq2000, 1×90 bp) and subsequent analysis of remaining rRNA reads from 10 ng untreated (Total RNA) and depleted A. thaliana RNA (1 ng, 100 ng, and 1 µg). The percentage of reads mapping to rRNA is plotted in blue.

Discover the complete plant transcriptome and sequence what matters to your experiment. RiboCop for Plants allows an unobstructed view of the transcriptome and increases gene detection at 3 M reads / sample by more than 45 % through efficient rRNA removal (Fig. 2).

Figure 2 | Increased gene detection upon rRNA depletionA. thaliana RNA samples were depleted with RiboCop for Plants using either 1 µg or 1 ng input RNA. Libraries were prepared using Lexogen’s CORALL RNA-Seq V2 Library Prep Kit and sequenced on Illumina NextSeq2000 (1×90 bp). Reads were mapped against the A. thaliana reference genome using STAR aligner and counted with FeatureCounts.

RiboCop enriches RNAs of interest across a range of different plant species (Fig. 3) and is suitable for depletion of various crops including corn (Zea mays), soybean (Glycine max), and others.

Figure 3 | RiboCop rRNA Depletion for Plants efficiently removes rRNA from A.thaliana, Z. mays, and G. max. NGS libraries were prepared using Lexogen’s CORALL RNA-Seq V2 Library Prep Kit. Successful depletion was monitored by NGS sequencing (NextSeq2000, 1×90 bp) and subsequent analysis of remaining rRNA reads from 5 ng untreated (Total RNA). 50 ng RNA from A. thaliana, Z. mays, and G. max were used for rRNA depletion prior to library generation. Reads were mapped to the respective reference genomes and the percentage of reads mapping to rRNA is plotted in blue.

Workflow

Samples are treated using a set of affinity probes for specific depletion of rRNA sequences. RiboCop probes efficiently remove rRNA and therefore afford a comprehensive view of transcriptome composition.

Step1:
Total time:
1hr 30min
Hands-on time:
30 min

Affinity probes and total RNA are mixed and denatured.

Denatured total RNA and probes are hybridized.

Depletion beads are conditioned and used to remove probes along with hybridized ribosomal RNA from solution.

The depleted RNA is purified for downstream processing.

FAQ

Frequently Asked Questions

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Downloads

Safety Data Sheet

If you need more information about our products, please contact us through support@lexogen.com or directly under +43 1 345 1212-41.

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