Evaluates the effectiveness of an optical RPA-CRISPR assay for detecting eDNA in conservation efforts, highlighting its practical applications.
-cleavage reaction in a single tube. The entire process is operated at a constant temperature, avoiding thermal cycling. Low-template replicate experiments conservatively redefined the OORC limit of detection as 6 copies/reaction. To support near-field application, we further integrated the assay with a portable handheld fluorescence detector capable of 365 nm photoactivation and fluorescence readout. This portable and highly sensitive workflow extends the potential of eDNA monitoring, offering a practical tool for the conservation of endangered species.
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Qiu et al. (2026) studied this question.
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