RNA EXPERTise Videos
RNA EXPERTise Videos
QuantSeq
Looking for an efficient gene expression profiling method? QuantSeq is a well-established 5-step mRNA-Seq library prep, finished in only 4.5 hours, and enabling highly multiplexed NGS experiments – even with FFPE samples!
QuantSeq-Pool
Looking for solution for gene expression profiling for large screening projects? QuantSeq-Pool mRNA-Seq library prep uniquely barcodes up to 96 samples in the first step and allows efficient batch processing. Simplify lab work, scale-up your transcriptome projects.
CORALL
Are you tired of lengthy and complicated whole transcriptome RNA-Seq library preparation protocols? CORALL is an all-in-one, fast, and robust whole transcriptome library prep kit that allows you to complete your RNA-Seq libraries in only 4.5 hours.
TraPR
Struggling with your small RNA-Seq experiments? TraPR offers a gel- and bias-free, column-based method for isolation of functional small RNAs from all organisms, even from challenging or inconsistent samples, cell types, tissues, and bio-fluids.
LUTHOR Technology
Do you want to explore further and detect more genes from one single cell? LUTHOR combines a revolutionary direct RNA amplification technology and a one-step 3’ library preparation method for unprecedented sensitivity and reproducibility in single-cell RNA-Seq.
RiboCop
Total RNA is comprised of large amounts of undesired ribosomal RNA (rRNA). RiboCop enables very efficient removal of rRNA. Besides ribosomal RNA, RiboCop can also deplete globin mRNA, which makes up 30 – 80 % of all mRNA in mammalian blood. Thus, RiboCop focuses sequencing reads on RNA of interest while maintaining unbiased expression profiles.
Spike-in RNA Variants (SIRVs)
Controls in RNA-Seq experiments are still widely overlooked, even though biases are introduced in virtually every step of an RNA-Seq experiment – from sampling to analysis – challenging reproducibility of results from RNA-Seq studies. Spike-In RNA Variant Control Mixes (SIRVs) mimic the natural complexity of transcriptomes, including length, concentration and isoform complexity. Therefore, SIRVs allow validation of complete RNA-Seq workflows and offer unique benefits for the identification and quantification of transcript isoforms facilitating transcriptome annotations.
Challenges and Best Practice in RNA-Sequencing
Looking for a quick guide into RNA-Seq? In this webinar, we will guide you through common challenges in RNA-Seq experiments, the importance of experimental design, and the right method for your experimental needs. Further, we introduce state-of-the art spike-in RNA variant (SIRV) controls and show how they can be used to ensure the success of your RNA-Seq experiments.
SLAMseq for High-Throughput Kinetic RNA Sequencing
Looking for an easy way to differentiate between direct and indirect targets of your drug candidates at high resolution? SLAMseq measures and monitors RNA kinetics in living cells in a time-resolved manner and combines RNA labeling with RNA sequencing to revolutionize your biochemical research or drug development.