Amplified Tandem Spinach-Based Aptamer Transcription Enables Low Background miRNA Detection

2018 ◽  
Vol 90 (16) ◽  
pp. 10001-10008 ◽  
Author(s):  
Xin Tang ◽  
Ruijie Deng ◽  
Yupeng Sun ◽  
Xiaojun Ren ◽  
Mengxi Zhou ◽  
...  
Author(s):  
R. B. Neder ◽  
M. Burghammer ◽  
Th. Grasl ◽  
H. Schulz

AbstractWe developed a small vacuum chamber for very low background single crystal diffraction experiments. The chamber has been designed for a large Eulerian cradle. The


1964 ◽  
Author(s):  
H. A. Wollenberg ◽  
A. R. Smith

Sensors ◽  
2021 ◽  
Vol 21 (12) ◽  
pp. 3985
Author(s):  
Nan Wan ◽  
Yu Jiang ◽  
Jiamei Huang ◽  
Rania Oueslati ◽  
Shigetoshi Eda ◽  
...  

A sensitive and efficient method for microRNAs (miRNAs) detection is strongly desired by clinicians and, in recent years, the search for such a method has drawn much attention. There has been significant interest in using miRNA as biomarkers for multiple diseases and conditions in clinical diagnostics. Presently, most miRNA detection methods suffer from drawbacks, e.g., low sensitivity, long assay time, expensive equipment, trained personnel, or unsuitability for point-of-care. New methodologies are needed to overcome these limitations to allow rapid, sensitive, low-cost, easy-to-use, and portable methods for miRNA detection at the point of care. In this work, to overcome these shortcomings, we integrated capacitive sensing and alternating current electrokinetic effects to detect specific miRNA-16b molecules, as a model, with the limit of detection reaching 1.0 femto molar (fM) levels. The specificity of the sensor was verified by testing miRNA-25, which has the same length as miRNA-16b. The sensor we developed demonstrated significant improvements in sensitivity, response time and cost over other miRNA detection methods, and has application potential at point-of-care.


Biosensors ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 222
Author(s):  
Chenxin Fang ◽  
Ping Ouyang ◽  
Yuxing Yang ◽  
Yang Qing ◽  
Jialun Han ◽  
...  

A microRNA (miRNA) detection platform composed of a rolling circle amplification (RCA) system and an allosteric deoxyribozyme system is proposed, which can detect miRNA-21 rapidly and efficiently. Padlock probe hybridization with the target miRNA is achieved through complementary base pairing and the padlock probe forms a closed circular template under the action of ligase; this circular template results in RCA. In the presence of DNA polymerase, RCA proceeds and a long chain with numerous repeating units is formed. In the presence of single-stranded DNA (H1 and H2), multi-component nucleic acid enzymes (MNAzymes) are formed that have the ability to cleave substrates. Finally, substrates containing fluorescent and quenching groups and magnesium ions are added to the system to activate the MNAzyme and the substrate cleavage reaction, thus achieving fluorescence intensity amplification. The RCA–MNAzyme system has dual signal amplification and presents a sensing platform that demonstrates broad prospects in the analysis and detection of nucleic acids.


2020 ◽  
Vol 1690 ◽  
pp. 012037
Author(s):  
O D Petrenko ◽  
A M Gangapshev ◽  
Yu M Gavrilyuk ◽  
V V Kazalov ◽  
V V Kuzminov ◽  
...  

2021 ◽  
Vol 413 (8) ◽  
pp. 2071-2079
Author(s):  
Yunwei Zhao ◽  
Hui Zhang ◽  
Ying Wang ◽  
Yanfang Zhao ◽  
Yaowei Li ◽  
...  

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