Issue 4, 2015

Parallel RNA extraction using magnetic beads and a droplet array

Abstract

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.

Graphical abstract: Parallel RNA extraction using magnetic beads and a droplet array

Article information

Article type
Paper
Submitted
23 Sep 2014
Accepted
09 Dec 2014
First published
18 Dec 2014
This article is Open Access
Creative Commons BY license

Lab Chip, 2015,15, 1059-1065

Author version available

Parallel RNA extraction using magnetic beads and a droplet array

X. Shi, C. Chen, W. Gao, S. Chao and D. R. Meldrum, Lab Chip, 2015, 15, 1059 DOI: 10.1039/C4LC01111B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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