Dual signal amplification by an “on-command” pure DNA hydrogel encapsulating HRP for colorimetric detection of ochratoxin A

RSC Advances ◽  
2016 ◽  
Vol 6 (115) ◽  
pp. 114500-114504 ◽  
Author(s):  
Lu Zhou ◽  
Na Sun ◽  
Lijun Xu ◽  
Xing Chen ◽  
Hui Cheng ◽  
...  

A pure DNA hydrogel, consisting of two kinds of Y-scaffold nucleic acid subunits and the aptamer domain of ochratoxin A, undergoes a switchable gel-to-sol transition in the presence of ochratoxin A.

2019 ◽  
Vol 186 (4) ◽  
Author(s):  
Weidan Chang ◽  
Weipeng Liu ◽  
Ying Liu ◽  
Fangfang Zhan ◽  
Huifang Chen ◽  
...  

2018 ◽  
Vol 9 (37) ◽  
pp. 7419-7425 ◽  
Author(s):  
Xiangdan Meng ◽  
Kai Zhang ◽  
Wenhao Dai ◽  
Yu Cao ◽  
Fan Yang ◽  
...  

We designed a porous 3D Au–DNA hydrogel network for simultaneously imaging multiplex miRNAs in living cells through dual-signal amplification.


The Analyst ◽  
2016 ◽  
Vol 141 (8) ◽  
pp. 2362-2366 ◽  
Author(s):  
Suping Li ◽  
Jianping Lai ◽  
Liming Qi ◽  
Muhammad Saqib ◽  
Saadat Majeed ◽  
...  

A simple and fast colorimetric method is developed for the sensitive and selective detection of Hg2+ based on a dual signal amplification strategy.


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.


2021 ◽  
Vol 334 ◽  
pp. 129682
Author(s):  
Xiujuan Qiao ◽  
Xin Ma ◽  
Xiaoyu Ma ◽  
Tianli Yue ◽  
Qinglin Sheng

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