Selected article for: "addition time and qrt PCR"

Author: Huang, Di; Shi, Zhuwei; Qian, Jiajie; Bi, Ke; Fang, Mengjun; Xu, Zhinan
Title: A CRISPR-Cas12a-Derived Biosensor Enabling Portable Personal Glucose Meter Readout for Quantitative Detection of SARS-CoV-2.
  • Cord-id: 5p9d1wlw
  • Document date: 2021_1_6
  • ID: 5p9d1wlw
    Snippet: SARS-CoV-2 has spread rapidly throughout the whole world and caused significant difficulties in the prevention and control of the epidemic. In this case, several detection methods have been established based on nucleic acid diagnostic techniques and immunoassays to achieve sensitive and specific detection of SARS-CoV-2. However, most methods are still largely dependent on professional instruments, highly trained operators, and centralized laboratories. These limitations gravely diminish their pr
    Document: SARS-CoV-2 has spread rapidly throughout the whole world and caused significant difficulties in the prevention and control of the epidemic. In this case, several detection methods have been established based on nucleic acid diagnostic techniques and immunoassays to achieve sensitive and specific detection of SARS-CoV-2. However, most methods are still largely dependent on professional instruments, highly trained operators, and centralized laboratories. These limitations gravely diminish their practicality and portability. Herein, a CRISPR Cas12a based assay was developed for portable, rapid and sensitive of SARS-CoV-2. In this assay, samples were quickly pretreated and amplified by reverse transcription recombinase-aided amplification (RT-RAA) under mild conditions. Then, by combining the CRISPR Cas12a system and a glucose-producing reaction, the signal of the virus was converted to that of glucose, which can be quantitatively read by a personal glucose meter in a few seconds. Nucleocapsid protein gene was tested as a model target, and the sensitivity for quantitative detection was as low as 10 copies/μL, which basically meet the needs of clinical diagnosis. In addition, with the advantages of lower material cost, shorter detection time, and no requirement for professional instrument in comparison with qRT-PCR, this assay is expected to provide a powerful technical support for the early diagnosis and intervention during epidemic prevention and control. This article is protected by copyright. All rights reserved.

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