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Detection of microRNAs by the combination of Exonuclease-III assisted target recycling amplification and repeated-fishing strategy.
Yan, Xiao-Mei; Wang, Yin-Qi; Chen, Yao; Chen, Zeng-Ping; Yu, Ru-Qin.
  • Yan XM; State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, PR China.
  • Wang YQ; State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, PR China.
  • Chen Y; Hunan Key Lab of Biomedical Materials and Devices, College of Life Sciences and Chemistry, Hunan University of Technology, Zhuzhou, 412008, PR China. Electronic address: chenyao717@hnu.edu.cn.
  • Chen ZP; State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, PR China. Electronic address: zpchen@hnu.edu.cn.
  • Yu RQ; State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan, 410082, PR China.
Anal Chim Acta ; 1131: 1-8, 2020 Sep 22.
Article en En | MEDLINE | ID: mdl-32928469
A simple but effective method for the detection of miRNAs was proposed by integrating exonuclease-III assisted target recycling amplification and repeated-fishing strategy. In the proposed method, exonuclease-III assisted target recycling amplification reaction is adopted to produce a large amount of DNA fragments with fluorescence group at its 5' end in the presence of the target miRNA, which are then repeatedly fished out from the reaction mixture by a gold foil modified with a capture probe and transferred into a so-called 'product tube'. The amount of the target miRNA can then be determined from the fluorescence measurement of the solution in the 'product tube'. Application to the detection of miRNA-155 in samples of KH-2 and BRSA-2B cells revealed that the proposed method could achieve sensitive and accurate quantification of the target miRNA with a limit of detection of 36 fM and recovery rates in the range from 96.2% to 105%. Its simplicity, sensitivity and resistance to possible fluorescence interferences in complex biological samples make the proposed method a potentially competitive alternative for miRNAs detection in complex biological samples.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Técnicas Biosensibles / MicroARNs Tipo de estudio: Diagnostic_studies Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Técnicas Biosensibles / MicroARNs Tipo de estudio: Diagnostic_studies Idioma: En Año: 2020 Tipo del documento: Article