| Literature DB >> 29286383 |
Jianwei Chen1, Ning Shao1, Jiaying Hu2, Rong Li2, Yuanshou Zhu1, Dabing Zhang3, Shujuan Guo1, Junhou Hui4, Peng Liu4, Litao Yang5, Sheng-Ce Tao6.
Abstract
Multi-target, short time, and resource-affordable methodologies for the detection of multiple nucleic acids in a single, easy to operate test are urgently needed in disease diagnosis, microbial monitoring, genetically modified organism (GMO) detection, and forensic analysis. We have previously described the platform called CALM (Capillary Array-based Loop-mediated isothermal amplification for Multiplex visual detection of nucleic acids). Herein, we describe improved fabrication and performance processes for this platform. Here, we apply a small, ready-to-use cassette assembled by capillary array for multiplex visual detection of nucleic acids. The capillary array is pre-treated into a hydrophobic and hydrophilic pattern before fixing loop-mediated isothermal amplification (LAMP) primer sets in capillaries. After assembly of the loading adaptor, LAMP reaction mixture is loaded and isolated into each capillary, due to capillary force by a single pipetting step. The LAMP reactions are performed in parallel in the capillaries. The results are visually read out by illumination with a hand-held UV flashlight. Using this platform, we demonstrate monitoring of 8 frequently appearing elements and genes in GMO samples with high specificity and sensitivity. In summary, the platform described herein is intended to facilitate the detection of multiple nucleic acids. We believe it will be widely applicable in fields where high-throughput nucleic acid analysis is required.Entities:
Mesh:
Substances:
Year: 2017 PMID: 29286383 PMCID: PMC5755395 DOI: 10.3791/56597
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355