Parallel RNA extraction using magnetic beads and a droplet array.

Lab Chip

Center for Biosignatures Discovery Automation, The Biodesign Institute, Arizona State University Tempe, Arizona, USA.

Published: February 2015

Nucleic acid extraction is a necessary step for most genomic/transcriptomic analyses, but it often requires complicated mechanisms to be integrated into a lab-on-a-chip device. Here, we present a simple, effective configuration for rapidly obtaining purified RNA from low concentration cell medium. This Total RNA Extraction Droplet Array (TREDA) utilizes an array of surface-adhering droplets to facilitate the transportation of magnetic purification beads seamlessly through individual buffer solutions without solid structures. The fabrication of TREDA chips is rapid and does not require a microfabrication facility or expertise. The process takes less than 5 minutes. When purifying mRNA from bulk marine diatom samples, its repeatability and extraction efficiency are comparable to conventional tube-based operations. We demonstrate that TREDA can extract the total mRNA of about 10 marine diatom cells, indicating that the sensitivity of TREDA approaches single-digit cell numbers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349128PMC
http://dx.doi.org/10.1039/c4lc01111bDOI Listing

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