Label-free visual detection of nucleic acids in biological samples with single-base mismatch detection capability

2012 ◽  
Vol 48 (4) ◽  
pp. 576-578 ◽  
Author(s):  
Yanling Song ◽  
Weiting Zhang ◽  
Yuan An ◽  
Liang Cui ◽  
Chundong Yu ◽  
...  
2005 ◽  
Vol 21 (6) ◽  
pp. 888-893 ◽  
Author(s):  
F. Fixe ◽  
V. Chu ◽  
D.M.F. Prazeres ◽  
J.P. Conde

Molecules ◽  
2019 ◽  
Vol 24 (3) ◽  
pp. 575 ◽  
Author(s):  
Jialun Han ◽  
Jincai Wu ◽  
Jie Du

Simple and rapid detection of DNA single base mismatch or point mutation is of great significance for the diagnosis, treatment, and detection of single nucleotide polymorphism (SNP) in genetic diseases. Homogeneous mutation assays with fast hybridization kinetics and amplified discrimination signals facilitate the automatic detection. Herein we report a quick and cost-effective assay for SNP analysis with a fluorescent single-labeled DNA probe. This convenient strategy is based on the efficient quenching effect and the preferential binding of graphene oxide (GO) to ssDNA over dsDNA. Further, a cationic comb-type copolymer (CCC), poly(l-lysine)-graft-dextran (PLL-g-Dex), significantly accelerates DNA hybridization and strand-exchange reaction, amplifying the effective distinction of the kinetic barrier between a perfect matched DNA and a mismatched DNA. Moreover, in vitro experiments indicate that RAW 264.7 cells cultured on PLL-g-Dex exhibits excellent survival and proliferation ability, which makes this mismatch detection strategy highly sensitive and practical.


2013 ◽  
Vol 5 (22) ◽  
pp. 6531 ◽  
Author(s):  
Nasrin Moradi ◽  
Mir Fazlollah Mousavi ◽  
Masoud Ayatollahi Mehrgardi ◽  
Abolhassan Noori

2018 ◽  
Vol 90 (13) ◽  
pp. 8102-8107 ◽  
Author(s):  
Qiufang Yang ◽  
Tingting Ai ◽  
You Lv ◽  
Yuqin Huang ◽  
Jia Geng ◽  
...  

Talanta ◽  
2019 ◽  
Vol 201 ◽  
pp. 358-363
Author(s):  
Wufan Pan ◽  
Dongdong Yu ◽  
Yazhou Qin ◽  
Wanghua Wu ◽  
Yuxiang Lu ◽  
...  

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