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Updated: Oct 3, 2026

Fluorescence detection methods for microfluidic droplet platforms
Published on: December 10, 2011
A microfluidic platform for transcription- and amplification-free detection of zepto-mole amounts of nucleic acid
Reinhard Mayr1, Michaela Haider1, Roland Thünauer1
1Center for Advanced Bioanalysis GmbH, Gruberstrasse 40-42, 4020 Linz, Austria.
Abstract:
Here we report the development of a device for the transcription- and amplification-free detection of DNA and RNA molecules down to the zepto-mole range. A microfluidic chip with a built-in microarray was used for manipulation of nano-liter sample volumes. Specific staining and immobilization of the target molecules was achieved via a double hybridization approach thereby avoiding bias due to enzymatic processes like reverse transcription and PCR amplification. Therefore, target molecules were indirectly labeled by pre-hybridization to complementary Cy5-labeled probes. The remaining single-stranded portion of each target molecule could subsequently hybridize to complementary capture probes of a microarray. Thus a target-mediated immobilization of labeled DNA took place. By means of an ultra-sensitive fluorescence readout, all molecules hybridized to the microarray could be detected. The combination of minimized sample volume and single molecule detection yielded a detection limit of 39 fM (831 molecules in 35.4 nl assay volume) for target DNA and 16 fM (338 molecules) for target RNA after 1h on-chip hybridization.

