ExpressPlex 2.0 Early Access: The workflow simplicity of one-step library prep combined with the performance of TnX for high throughput sequencing of plasmids, amplicons and other synthetic constructs.
ExpressPlex 2.0 is an automation-friendly, one-step library prep powered by TnX to reduce bias and improve coverage uniformity using a highly streamlined workflow for sequencing plasmids, amplicons and other synthetic constructs.
– Zachary Neuschaefer, Principal NGS Engineer, LifeMine Therapeutics
ExpressPlex 2.0 uses tagmentation powered by TnX, the next generation transposase, to simultaneously fragment & index sample DNA. Average fragment size ranges from 400-1200 bp.
ExpressPlex 2.0 is the only library prep kit powered by TnX! TnX was engineered to reduce insertional bias to improve uniformity of coverage. When directly compared to a Tn5-based competitor library prep kit for sequencing of 2 different plasmids, ExpressPlex 2.0 produced significantly lower CVs and range of coverage (max/min).
The game-changing capabilities enabled by the ExpressPlex workflow were highlighted in a webinar collaboration with the synthetic biology team from Octant Bio, a drug discovery company located in Emeryville, CA. Octant’s Henry Chan, PhD (Synthetic Biology Lead) and Bryan Jiang (Research Associate) discussed the application of ExpressPlex to OCTOPUS, the high-throughput plasmid sequencing platform that powers Octant’s therapeutic discovery platform. Watch the video to discover how ExpressPlex has dramatically improved OCTOPUS and accelerated their overall discovery process.
The automation-friendly ExpressPlex one-step tagmentation workflow enables a >80% reduction in tips/plastics usage. We help drive sustainability not only in our internal sequencing services pipeline, but for our customers across the globe.
ExpressPlex 2.0 Specifications | |
Primary Applications | Plasmid and amplicon sequencing |
Sample Input types | Purified plasmid DNA, RCA-amplified DNA, amplicons >350bp, colony PCR amplicons |
Transposase | TnX – Next generation engineered transposase |
Reactions per Kit |
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DNA Input Recommended | 1-40ng |
Total Library Prep Time | 100 minutes (30 minutes hands-on time) |
Indexing Method | Combinatorial Dual Indexing |
Number of Unique Index Combinations | 1536 |
Batch Size | 48-96 samples per batch |
Output Fragment Range* | 400 – 1,200bp |
Number of PCR Cycles |
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Sequencer Compatibility |
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* Fragment size will depend on magnetic bead cleanup ratios used.