Sequence Validation: A Simple Step to Ensure Experimental Outcomes & Therapeutic Safety.

Plasmids are invaluable tools that underpin a wide range of applications across research, biotechnology, and medicine. Equally important to plasmid design is the rigorous validation of plasmid sequences before use them, as even small errors can compromise outcomes.

 

  • Therapeutic development – gene therapies, monoclonal antibodies, and mRNA vaccine production
  • Synthetic biology – driving the DBTL (design-build-test-learn) cycle for systematic engineering of biological systems
  • Protein production – high-yield expression of recombinant proteins, antibodies, and enzymes
  • Gene editing – delivery of CRISPR-Cas components and other editing tools
  • Agricultural biotechnology – engineering plants and microbes for improved traits and crop protection
  • Metabolic engineering – optimizing microbial strains for biofuel, biomaterial, and pharmaceutical synthesis
  • Functional genomics – overexpression, knockdown, and reporter assays for studying gene function

SHORT-READ & LONG-READ Sequencing Solutions

seqWell offers tagmentation-based library prep workflow solutions for both SHORT- and LONG-read sequencers to drive simplescalable and cost-effective plasmid and amplicon sequencing.  All our workflows are easy to implement and automation-friendly!

  • ExpressPlex 2.0 Library Preparation Kit – one-step TnX tagmentation with auto-normalization for high-throughput, short-read sequencing
  • LongPlex Multiplexing Kit – tagmentation-based fragmentation & multiplexing for long-read sequencing

Simple workflowS

Tagmentation simultaneously fragments & indexes sample DNA

SCALABLE

Automation-friendly, highly multiplexed library prep

COST EFFECTIVE

Large reductions in labor and consumables without sacrificing quality

RECORDED WEBINAR

Moderna presentation – Antibody Sequencing: New Operating Model

In this presentation, Nasthas Lacerda Almeida from Moderna, highlights how her organization has leveraged ExpressPlex™ 2.0 for a clonal antibody sequencing approach, optimized for speed and scalability using de novo assembly of NGS short reads.

Watch Now

Save > 80% on High-Throughput Library Prep With ExpressPlex 2.0

Do you know the true cost of your NGS library prep once labor, consumables, and add-ons are included?  With ExpressPlex™ 2.0, those extras disappear!

HIDDEN SAVINGS, CLEAR VALUE
✔️ 90% labor savings
✔️ 90% fewer consumables
✔️ Kit includes indexes & purification beads

Explore the Cost Savings!

Learn More With These Blogs

Why are 6144, 384 & 100 Magic Numbers in Synthetic Biology?

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Short-Read Sequencing vs. Long-Read Sequencing: Which Technology is Right for Your Research?

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