纳米孔
放大器
化学
DNA
纳米孔测序
碱基对
聚合酶链反应
纳米技术
生物物理学
基因
生物
DNA测序
材料科学
生物化学
作者
Huizhen Li,Yunhui Li,Cenlin Gui,Daqi Chen,Lanfang Chen,Le Luo,Guobao Huang,Yuan Yang,Rong He,F. Xia,Jiahai Wang
出处
期刊:Talanta
[Elsevier]
日期:2023-05-01
卷期号:256: 124275-124275
被引量:6
标识
DOI:10.1016/j.talanta.2023.124275
摘要
In this study, it is confirmed that without addition of organic solvent and embedding polymer hydrogel into glass nanopore, bare glass nanopore can faithfully measure various lengths of DNA duplexes from 200 to 3000 base pairs with 200 base pairs resolution, showing well-separated peak amplitudes of blockage currents. Furthermore, motivated by this readout capability of duplex DNA, amplicons from Polymerase Chain Reaction (PCR) amplification are straightforwardly discriminated by bare glassy nanopore without fluorescent labeling. Except simultaneous discrimination of up to 7 different segments of the same lambda genome, various pathogenic bacteria and viruses including SARS-CoV-2 and its mutants in clinical samples can be discriminated at high resolution. Moreover, quantitative measurement of PCR amplicons is obtained with detection range spanning from 0.75 aM to 7.5 pM and detection limit of 7.5 aM, which reveals that bare glass nanopore can faithfully disclose PCR results without any extra labeling.
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