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Updated: Sep 4, 2026

Probe-based Real-time PCR Approaches for Quantitative Measurement of microRNAs
Published on: April 14, 2015
Duplex-Specific DNase Signal Amplification Allows Attomolar Electrochemical Detection of MicroRNAs
Vatsala Pithaih1,2,3, Henry F F Bellette1,2,3, Thiago C Pimenta1,2,3
1The Biomedical and Environmental Sensor Technology (BEST) Research Centre, La Trobe Institute for Molecular Science (LIMS), La Trobe University, Melbourne, Victoria, 3086, Australia.
Abstract:
Point-of-care biosensors for detecting blood-circulating nucleic acids hold significant potential for disease diagnosis. However, achieving both high sensitivity and accessibility remains a challenge. Electrochemical hybridization assays offer a promising approach for detecting specific nucleic acid sequences but are typically limited to picomolar concentrations. Here, a duplex-specific DNase-assisted electrochemical hybridization assay is presented, enabling highly sensitive nucleic acid detection. By incorporating duplex DNase, the method achieves detection limits as low as 1 attomolar, significantly enhancing sensitivity. This work paves the way for ultrasensitive nucleic acid detection in critical point-of-care applications.
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