Au Nanoparticles–3D Graphene Hydrogel Nanocomposite To Boost Synergistically in Situ Detection Sensitivity toward Cell-Released Nitric Oxide

2015 ◽  
Vol 7 (4) ◽  
pp. 2726-2734 ◽  
Author(s):  
Jialin Li ◽  
Jiale Xie ◽  
Lixia Gao ◽  
Chang Ming Li
RSC Advances ◽  
2014 ◽  
Vol 4 (1) ◽  
pp. 369-373 ◽  
Author(s):  
Shurong Wang ◽  
Hongxin Zhang ◽  
Yanshuang Wang ◽  
Liwei Wang ◽  
Zhe Gong

2021 ◽  
Author(s):  
Luke Lee ◽  
Fei Liu ◽  
Yuchao Chen ◽  
Gianluca Roma

Abstract The COVID-19 pandemic has become an immense global health crisis. However, the lack of efficient and sensitive on-site testing methods limits early detection for timely isolation and intervention. Here, we present a Quantitative and Ultrasensitive in-situ Immunoassay Technology for SARS-CoV-2 detection in saliva (QUIT SARS-CoV-2). Our nanoporous membrane resonator generates a rapid oscillating flow to purify and concentrate SARS-CoV-2 virus in saliva by 40 folds for in-situ detection of viral antigens based on chemiluminescent immunoassay within 20 min. This method achieved a detection sensitivity below 10 0 copies/mL viral load, comparable to the bench-top PCR equipment. The portable QUIT SARS-CoV-2 system, allowing rapid and accurate on-site viral screen with high-throughput sample pooling strategy, can be performed at the primary care settings and substantially improve the detection and prevention of COVID-19.


2001 ◽  
Vol 281 (2) ◽  
pp. C726-C732 ◽  
Author(s):  
Rajesh Kher ◽  
Robert Bacallao

In situ hybridization has been used for localization of specific nucleic acid sequences at the cellular level despite providing relatively low-detection sensitivity. In situ reverse transcriptase-polymerase chain reactions (RT-PCR) enhance sensitivity and thus enable localization of low-abundance mRNA in a cell. However, the available methods are fraught with problems of nonspecific amplifications as a result of mispriming and/or amplification from partially digested residual genomic DNA in tissue. Herein, we demonstrate that nonspecific background amplification can be eliminated by pretreatment of samples with restriction enzymes before DNase I digestion. Primers tagged with a far-red shifted fluorescent dye such as Cy5 in PCR reactions allow identification of target mRNA by fluorescence microscopy. These novel modifications lead to increased specificity and rapid in situ detection of cellular mRNA and thus may be used for pathological diagnosis.


2017 ◽  
Vol 244 ◽  
pp. 1037-1044 ◽  
Author(s):  
Yanan Zhao ◽  
Danqun Huo ◽  
Jing Bao ◽  
Mei Yang ◽  
Mei Chen ◽  
...  

Langmuir ◽  
2008 ◽  
Vol 24 (21) ◽  
pp. 12112-12115 ◽  
Author(s):  
Jaemoon Yang ◽  
Kilho Eom ◽  
Eun-Kyung Lim ◽  
Jinsung Park ◽  
Yoonah Kang ◽  
...  

2003 ◽  
pp. 227-238
Author(s):  
Pei Tsai ◽  
Supatra Porasuphatana ◽  
Howard J. Halpern ◽  
Eugene D. Barth ◽  
Gerald M. Rosen

Nanoscale ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 4471-4477 ◽  
Author(s):  
Yuhuan Zhang ◽  
Shi-Yu Lu ◽  
Zhuanzhuan Shi ◽  
Zhi Liang Zhao ◽  
Qian Liu ◽  
...  

Core–cage Cu2O@FePO4 nanocomposites for the highly sensitive in situ detection of nitric oxide.


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