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One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a
by
Chen, Wei
, Li, Dechang
, Sun, Yangyang
, Huang, Weiren
, Yu, Lei
, Liu, Chengxi
, Ye, Shanting
in
Acids
/ Aerosols
/ Base Sequence
/ Biomedical and Life Sciences
/ Biomedicine
/ Coronaviridae
/ Coronaviruses
/ COVID-19
/ COVID-19 - diagnosis
/ COVID-19 - virology
/ COVID-19 Testing - methods
/ CRISPR
/ CRISPR-Cas Systems - genetics
/ CRISPR/Cas
/ Endonuclease
/ Epidemics
/ Fever
/ Gene amplification
/ Humans
/ Influenza A
/ Laboratories
/ Limit of Detection
/ Medical research
/ Medicine, Experimental
/ Medicine/Public Health
/ Polymerase chain reaction
/ Real-Time Polymerase Chain Reaction - methods
/ Recombinase
/ Reference Standards
/ Reverse transcription
/ Reverse Transcription - genetics
/ Ribonucleic acid
/ RNA
/ RNA, Viral - genetics
/ RT-RPA
/ SARS-CoV-2 - genetics
/ SARS-CoV-2 - isolation & purification
/ SARS-CoV-2 assay
/ Severe acute respiratory syndrome coronavirus 2
/ Translational Genomics and Genetics
2021
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One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a
by
Chen, Wei
, Li, Dechang
, Sun, Yangyang
, Huang, Weiren
, Yu, Lei
, Liu, Chengxi
, Ye, Shanting
in
Acids
/ Aerosols
/ Base Sequence
/ Biomedical and Life Sciences
/ Biomedicine
/ Coronaviridae
/ Coronaviruses
/ COVID-19
/ COVID-19 - diagnosis
/ COVID-19 - virology
/ COVID-19 Testing - methods
/ CRISPR
/ CRISPR-Cas Systems - genetics
/ CRISPR/Cas
/ Endonuclease
/ Epidemics
/ Fever
/ Gene amplification
/ Humans
/ Influenza A
/ Laboratories
/ Limit of Detection
/ Medical research
/ Medicine, Experimental
/ Medicine/Public Health
/ Polymerase chain reaction
/ Real-Time Polymerase Chain Reaction - methods
/ Recombinase
/ Reference Standards
/ Reverse transcription
/ Reverse Transcription - genetics
/ Ribonucleic acid
/ RNA
/ RNA, Viral - genetics
/ RT-RPA
/ SARS-CoV-2 - genetics
/ SARS-CoV-2 - isolation & purification
/ SARS-CoV-2 assay
/ Severe acute respiratory syndrome coronavirus 2
/ Translational Genomics and Genetics
2021
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One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a
by
Chen, Wei
, Li, Dechang
, Sun, Yangyang
, Huang, Weiren
, Yu, Lei
, Liu, Chengxi
, Ye, Shanting
in
Acids
/ Aerosols
/ Base Sequence
/ Biomedical and Life Sciences
/ Biomedicine
/ Coronaviridae
/ Coronaviruses
/ COVID-19
/ COVID-19 - diagnosis
/ COVID-19 - virology
/ COVID-19 Testing - methods
/ CRISPR
/ CRISPR-Cas Systems - genetics
/ CRISPR/Cas
/ Endonuclease
/ Epidemics
/ Fever
/ Gene amplification
/ Humans
/ Influenza A
/ Laboratories
/ Limit of Detection
/ Medical research
/ Medicine, Experimental
/ Medicine/Public Health
/ Polymerase chain reaction
/ Real-Time Polymerase Chain Reaction - methods
/ Recombinase
/ Reference Standards
/ Reverse transcription
/ Reverse Transcription - genetics
/ Ribonucleic acid
/ RNA
/ RNA, Viral - genetics
/ RT-RPA
/ SARS-CoV-2 - genetics
/ SARS-CoV-2 - isolation & purification
/ SARS-CoV-2 assay
/ Severe acute respiratory syndrome coronavirus 2
/ Translational Genomics and Genetics
2021
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One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a
Journal Article
One-tube SARS-CoV-2 detection platform based on RT-RPA and CRISPR/Cas12a
2021
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Overview
Background
COVID-19 has spread rapidly around the world, affecting a large percentage of the population. When lifting certain mandatory measures for an economic restart, robust surveillance must be established and implemented, with nucleic acid detection for SARS-CoV-2 as an essential component.
Methods
We tried to develop a one-tube detection platform based on RT-RPA (Reverse Transcription and Recombinase Polymerase Isothermal Amplification) and DNA Endonuclease-Targeted CRISPR Trans Reporter (DETECTR) technology, termed OR-DETECTR, to detect SARS-CoV-2. We designed RT-RPA primers of the RdRp and N genes following the SARS-CoV-2 gene sequence. We optimized reaction components so that the detection process could be carried out in one tube. Specificity was demonstrated by detecting nucleic acid samples from pseudoviruses from seven human coronaviruses and Influenza A (H1N1). Clinical samples were used to validate the platform and all results were compared to rRT-PCR. RNA standards and pseudoviruses diluted by different gradients were used to demonstrate the detection limit. Additionally, we have developed a lateral flow assay based on OR-DETECTR for detecting COVID-19.
Results
The OR-DETECTR detection process can be completed in one tube, which takes approximately 50 min. This method can specifically detect SARS-CoV-2 from seven human coronaviruses and Influenza A (H1N1), with a low detection limit of 2.5 copies/µl input (RNA standard) and 1 copy/µl input (pseudovirus). Results of six samples from SARS-CoV-2 patients, eight samples from patients with fever but no SARS-CoV-2 infection, and one mixed sample from 40 negative controls showed that OR-DETECTR is 100% consistent with rRT-PCR. The lateral flow assay based on OR-DETECTR can be used for the detection of COVID-19, and the detection limit is 2.5 copies/µl input.
Conclusions
The OR-DETECTR platform for the detection of COVID-19 is rapid, accurate, tube closed, easy-to-operate, and free of large instruments.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
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