数字聚合酶链反应
色谱法
多路复用
检出限
聚合酶链反应
环介导等温扩增
多重聚合酶链反应
化学
微流控
分子生物学
食品科学
计算生物学
DNA
生物
生物化学
纳米技术
材料科学
遗传学
基因
作者
Chengzhuang Yu,Shijie Dai,Ziqi Zhang,Shanshan Li,Jingmeng Cheng,Hezhi Hu,Jie Wu,Junwei Li
出处
期刊:Electrophoresis
[Wiley]
日期:2023-06-13
卷期号:44 (17-18): 1342-1352
被引量:6
标识
DOI:10.1002/elps.202200188
摘要
Meat adulteration detection is a common concern of consumers. Here, we proposed a multiplex digital polymerase chain reaction method and a low-cost device for meat adulteration detection. Using a polydimethylsiloxane microfluidic device, polymerase chain reaction reagents could be pump-free loaded into microchambers (40 × 40 chambers) automatically. Due to the independence of multiplex fluorescence channels, deoxyribonucleic acid templates extracted from different animal species could be distinguished by one test. In this paper, we designed primers and probes for four types of meat (beef, chicken, pork, and duck) and labeled each of the four fluorescent markers (hexachlorocyclohexane [HEX], 6-carboxyfluorescein [FAM], X-rhodamine [ROX], and cyanine dyes 5 [CY5]) on the probes. Specific detection and mixed detection experiments were performed on four types of meat, realizing a limit of detection of 3 copies/µL. A mixture of four different species can be detected by four independent fluorescence channels. The quantitative capability of this method is found to meet the requirements of meat adulteration detections. This method has great potential for point-of-care testing together with portable microscopy equipment.
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