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10.1039/d1lc00293g

http://scihub22266oqcxt.onion/10.1039/d1lc00293g
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34100058!8277744!34100058
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suck abstract from ncbi


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pmid34100058      Lab+Chip 2021 ; 21 (14): 2730-2737
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  • Autonomous lab-on-paper for multiplexed, CRISPR-based diagnostics of SARS-CoV-2 #MMPMID34100058
  • Yin K; Ding X; Li Z; Sfeir MM; Ballesteros E; Liu C
  • Lab Chip 2021[Jul]; 21 (14): 2730-2737 PMID34100058show ga
  • The COVID-19 pandemic, caused by severe acute respiratory coronavirus 2 (SARS-CoV-2), has become a public health emergency and widely spread around the world. Rapid, accurate and early diagnosis of COVID-19 infection plays a crucial role in breaking this pandemic. However, the detection accuracy is limited for current single-gene diagnosis of SARS-CoV-2. Herein, we develop an autonomous lab-on-paper platform for multiplex gene diagnosis of SARS-CoV-2 by combining reverse transcription recombinase polymerase amplification (RT-RPA) and CRISPR-Cas12a detection. The autonomous lab-on-paper is capable of simultaneously detecting nucleoprotein (N) gene and spike (S) gene of SARS-CoV-2 virus as well as human housekeeping RNAse P gene (an internal control) in a single clinical sample. With the developed platform, 102 copies viral RNA per test can be detected within one hour. Also, the lab-on-paper platform has been used to detect 21 swab clinical samples and obtains a comparable performance to the conventional RT-PCR method. Thus, the developed lab-on-paper platform holds great potential for rapid, sensitive, reliable, multiple molecular diagnostics of COVID-19 and other infectious diseases in resource-limited settings.
  • |*COVID-19[MESH]
  • |*Pandemics[MESH]
  • |CRISPR-Cas Systems/genetics[MESH]
  • |Clustered Regularly Interspaced Short Palindromic Repeats[MESH]
  • |Humans[MESH]
  • |Nucleic Acid Amplification Techniques[MESH]
  • |RNA, Viral/genetics[MESH]
  • |SARS-CoV-2[MESH]


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