Multiplex ligation-dependent probe amplification (MLPA) for ultrasensitive multiplexed microRNA detection using ribonucleotide-modified DNA probes

2013 ◽  
Vol 49 (85) ◽  
pp. 10013 ◽  
Author(s):  
Pengbo Zhang ◽  
Ye Liu ◽  
Yajing Zhang ◽  
Chenghui Liu ◽  
Zhibin Wang ◽  
...  
2019 ◽  
Vol 55 (62) ◽  
pp. 9104-9107 ◽  
Author(s):  
Tongxu Gu ◽  
Zhaohui Ren ◽  
Xiang Li ◽  
Jie Huang ◽  
Gaorong Han

We have developed a photoluminescent membrane for microRNA detection, consisting of mesoporous silica nanoparticles (CaF2:Yb/Ho@MSNs) attached, via single stranded DNA probes, to flexible polyurethane fibres coated with graphene oxide (GO).


Author(s):  
A. K. Raap ◽  
R. W. Dirks ◽  
N. M. Jiwa ◽  
P. M. Nederlof ◽  
M. van der Ploeg

2021 ◽  
Vol 12 ◽  
Author(s):  
Yuxuan He ◽  
Likun Long ◽  
Wei Yan ◽  
Liming Dong ◽  
Wei Xia ◽  
...  

Microribonucleic acids (miRNAs) play significant roles in the regulation of biological processes and in responses to biotic or abiotic environmental stresses. Therefore, it is necessary to quantitatively detect miRNAs to understand these complicated biological regulation mechanisms. This study established an ultrasensitive and highly specific method for the quantitative detection of miRNAs using simple operations on the ground of the ligation reaction of ribonucleotide-modified deoxyribonucleic acid (DNA) probes. This method avoids the complex design of conventional reverse transcription. In the developed assay, the target miRNA miR156b was able to directly hybridize the two ribonucleotide-modified DNA probes, and amplification with universal primers was achieved following the ligation reaction. As a result, the target miRNA could be sensitively measured even at a detection limit as low as 0.0001 amol, and differences of only a single base could be detected between miR156 family members. Moreover, the proposed quantitative method demonstrated satisfactory results for overexpression-based genetically modified (GM) soybean. Ligation-based quantitative polymerase chain reaction (PCR) therefore has potential in investigating the biological functions of miRNAs, as well as in supervising activities regarding GM products or organisms.


ACS Nano ◽  
2012 ◽  
Vol 6 (10) ◽  
pp. 8803-8814 ◽  
Author(s):  
Pratik Shah ◽  
Andreas Rørvig-Lund ◽  
Samir Ben Chaabane ◽  
Peter Waaben Thulstrup ◽  
Henrik Grum Kjaergaard ◽  
...  

Talanta ◽  
2018 ◽  
Vol 183 ◽  
pp. 11-17 ◽  
Author(s):  
Jing Li ◽  
Jin Huang ◽  
Xiaohai Yang ◽  
Yanjing Yang ◽  
Ke Quan ◽  
...  

2006 ◽  
Vol 20 (5) ◽  
Author(s):  
Richard Owczarzy ◽  
Yong You ◽  
Bernardo G. Moreira ◽  
Mark A. Behlke

1997 ◽  
Vol 5 (6) ◽  
pp. 1037-1042 ◽  
Author(s):  
Andrew T. Daniher ◽  
Jin Xie ◽  
Shashank Mathur ◽  
James K. Bashkin

2014 ◽  
Vol 86 (14) ◽  
pp. 6823-6826 ◽  
Author(s):  
Thomas Christian de Bang ◽  
Pratik Shah ◽  
Seok Keun Cho ◽  
Seong Wook Yang ◽  
Søren Husted

2006 ◽  
Vol 352 (2) ◽  
pp. 188-197 ◽  
Author(s):  
Martin Dufva ◽  
Jesper Petersen ◽  
Michael Stoltenborg ◽  
Henrik Birgens ◽  
Claus B.V. Christensen

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