Xpedite Diagnostics brought together experts from the University of Marburg and its in-house R&D team for a technical masterclass on RAA/RPA assay design, highlighting how isothermal amplification is reshaping rapid, portable molecular diagnostics for field and point-of-care settings.
Fast, Field-Ready Assay Design
Dr. Till Adhikary opened the session with a practical walkthrough of RT-RAA workflows for RNA virus detection. Drawing on his COVID-19 assay development experience, he demonstrated how primer length, probe design, and recombinase activity drive fast amplification at body-temperature ranges. His optimized RT-RAA assays delivered clear results within 15 minutes, demonstrating how low-temperature amplification can support decentralized testing.
Duplex RAA for Schistosoma Detection
Xpedite’s Ejona Gjika presented the development of a duplex RAA assay for Schistosoma mansoni and S. haematobium. After identifying performance limits in published singleplex assays, the team adapted the SM1-7 genomic repeat into an RAA-compatible format, achieving sensitivity down to 120 copies in 10 minutes. Validation against qPCR and microscopy confirmed strong correlation and field applicability.
Building the Portable Diagnostics Ecosystem
The speakers showcased Xpedite’s integrated isothermal toolkit, from SwiftX™ extraction and Ketian reagents to steel-bead auto-mixing and the Axon Reader, enabling fully portable workflows for environmental surveillance, parasitology, and infectious disease diagnostics.
As the session highlighted, isothermal NAATs now offer a fast, sensitive, infrastructure-light alternative to PCR—, bringing molecular diagnostics closer to where they’re needed most.
- Watch the full webinar recording [here]
- Access the slides:
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Design of a SARS-CoV2 RT-RPA rapid test with LFD detection (Dr. Till Adhikary)
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Development of a duplex RAA for Schistosoma detection (Ejona Gjika)
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