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Jung-Chung Lin b Division of Infectious Diseases and Tropical Medicine, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei,. In particular, using real-time RT-PCR with the lab-developed PCR assay and the BD Max system, we detected 55 samples as positive and 150 samples as negative for SARS-CoV-2..


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The use of RT-LAMP (reverse transcriptase—loop mediated isothermal amplification) has been considered as a promising point-of-care method to diagnose COVID-19. In this manuscript we show that.


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Analysis of the results, in comparison to RT-qPCR, found that the ZIKV RT-LAMP assay provided sensitivity of 100%, specificity of 93.75%, and an overall accuracy of 95.00%.


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Here we provide detailed technical data and evaluate the performance of three novel rRT-PCR assays targeting the ORF1ab, N, and E genes for detection of COVID-19 infection. The application of rRT-PCR assays among four types of specimens (alveolar lavage, sputum, throat swabs, and stool) from patients with COVID-19 indicated that the mean viral.


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Schematics of RT-LAMP amplification, exemplified for SARS-CoV-2detection.. Reverse transcription loop-mediated isothermal amplification (RT-LAMP) is a one step nucleic acid amplification method to multiply specific sequences of RNA.It is used to diagnose infectious disease caused by RNA viruses.. It combines LAMP DNA-detection with reverse transcription, making cDNA from RNA before running the.


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The real-time RT-PCR master mixture in a 25 μl volume was optimized, and the mixture consisted of 12.5 μl of 2 × one-step RT-PCR buffer, 0.5 μl of Ex Taq HS, 0.5 μl of RT Enzyme Mix II, 0.5 μl of each primer and probe, 5 μl of RNA/DNA template, and finally RNase-free water was added for a total volume of 25 μl in each reaction tube.


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Plant materials. To develop single and multiplex RT-LAMP assays, we collected plant material from various Musa genotypes growing at the Waimanalo Research Station, College of Tropical Agriculture and Human Resources (CTAHR), University of Hawaii at Manoa, located in Honolulu County, HI, USA. The material included twelve samples from plants with typical symptoms of banana bunchy top disease.


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RT-LAMP could be used for SARS-CoV-2 testing and overcomes the challenges of adapting an assay to a point-of-care instrument. Further, the reduced instrumentation cost and complexity, along with the simple workflow, highlight the potential for implementation of RT-LAMP for SARS-CoV-2 testing in resource-limited settings.


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Background Children are the most vulnerable group affected by malaria and other tropical, vector-borne diseases in low-resource countries. Infants presenting with acute onset fever represent a major sector of outpatient care in the Lake Victoria region. Misclassification and overuse of antibiotics and anti-malarial medications are consistent problems. Identifying the prevalent mosquito-borne.


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The RNAzol RT reagent was used to provide pure RNA from human cells. We develop a protocol using RNAzol RT reagent to extract pure RNA from plants tissues and demonstrate that this RNA extraction method works not only at room temperature but also at elevated temperatures and provides the simplest and most effective single-step method to extract pure and undegraded RNA directly from tropical.


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The global COVID-19 pandemic has highlighted the need for rapid, accurate and accessible nucleic acid tests to enable timely identification of infected individuals. We optimized a sample-to-answer nucleic acid test for SARS-CoV-2 that provides results in <1 hour using inexpensive and readily available reagents. The test workflow includes a simple lysis and viral inactivation protocol followed.


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