| Literature DB >> 29595058 |
Weifei Zhang1,2, Nan Li2, Daisuke Koga1, Yong Zhang1, Hulie Zeng1, Hizuru Nakajima1, Jin-Ming Lin2, Katsumi Uchiyama1.
Abstract
We report on the development of a novel and flexible online digital polymerase chain reaction (dPCR) system. The system was composed of three parts: an inkjet for generating the droplets, a coiled fused-silica capillary for thermal cycling, and a laser-induced fluorescence detector (LIFD) for positive droplet counting. Upon inkjet printing, monodisperse droplets were continuously generated in the oil phase and then introduced into the capillary in the form of a stable dispersion. The droplets containing one or zero molecules of target DNA passed through the helical capillary that was attached to a cylindrical thermal cycler for PCR amplification, resulting in the generation of fluorescence for the DNA-positive droplet. After 36 PCR cycles, the fluorescence signal intensity was detected by laser-induced fluorescence located at the downstream of the capillary, followed by a positive/negative counting. The present system was successfully applied to the absolute quantification of the HPV sequence in Caski cells with dynamic ranges spanning 4 orders of magnitude.Entities:
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Year: 2018 PMID: 29595058 DOI: 10.1021/acs.analchem.8b00463
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986