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Anal Chem. 2012 Aug 7;84(15):6366-9. doi: 10.1021/ac301586q. Epub 2012 Jul 16.

Integration of on-chip isotachophoresis and functionalized hydrogels for enhanced-sensitivity nucleic acid detection.

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Department of Mechanical Engineering, Stanford University, Stanford, California 94305, USA.


We introduce an on-chip electrokinetic assay to perform high-sensitivity nucleic acid (NA) detection. This assay integrates electrokinetic sample focusing using isotachophoresis (ITP) with a background signal-removal strategy that employs photopatterened, DNA-functionalized hydrogels. In this multistage assay, ITP first enhances hybridization kinetics between target NAs and end-labeled complementary reporters. After enhanced hybridization, migration through a DNA-functionalized hydrogel region removes excess reporters through affinity interactions. We demonstrate our assay on microRNAs, an important class of low-abundance biomarkers. The assay exhibits 4 orders of magnitude dynamic range, near 1 pM detection limits starting from less than 100 fg of microRNA, and high selectivity for mature microRNA sequences, all within a 10 min run time. This new microfluidic framework provides a unique quantitative assay for NA detection.

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