Ratiometric fluorescent detection and imaging of microRNA in living cells with manganese dioxide nanosheet-active DNAzyme

Talanta ◽  
2021 ◽  
pp. 122518
Author(s):  
Yuan Zhang ◽  
Chunmeng Ma ◽  
Chen Ma ◽  
Yueci Xiang ◽  
Shuai Mu ◽  
...  
2021 ◽  
Author(s):  
Ali Qaitoon ◽  
Jiaxi Yong ◽  
Zexi Zhang ◽  
Jie Liu ◽  
Zhi Ping Xu ◽  
...  

Tripeptide glutathione (GSH) is an abundant and ubiquitous metabolite in living organisms and plays critical roles in various cellular processes. In this work, we report the development of a new...


2022 ◽  
pp. 132382
Author(s):  
Xiao-Chuang Chang ◽  
Xue-Feng Han ◽  
Bing-Jie Liu ◽  
Zi-Yi Jiang ◽  
Shuai-Ze Li ◽  
...  

2022 ◽  
Author(s):  
luo wentao ◽  
Zhiyang Yuwen ◽  
Hui Li ◽  
Shouzhi Pu

A novel colorimetric/fluorescent chemosensor (1o) was designed and synthesized for the detection of CN- and Al3+. 1o exhibited a selective dual channel response to CN-, while it showed fluorescence changes...


2018 ◽  
Vol 14 (5) ◽  
pp. 1788-1789
Author(s):  
Kaixuan Liang ◽  
Yajun Sun ◽  
Kezheng Chen ◽  
Wei Wang

1976 ◽  
Vol 24 (1) ◽  
pp. 24-33 ◽  
Author(s):  
S A Latt ◽  
G Stetten

Absorption, fluroescence and circular dichroism measrements on 33258 Hoechst-deoxyribonucleic acid (DNA) complexes are consistent with the existence of two types of dye-binding interactions. One type, which persists at elevated solution ionic strength, is highly specific for adenine-thymine-rich DNA. Dye bound under this condition exhibits efficient fluorescence and strong optical activity. A less specific, largely electrostatic interaction is associated with less intense fluorescence and weaker optical activity. The fluorescence of 33258 Hoechst and several other bisbenzimidazole dyes is less when bound to poly(deoxyadenylate-5-bromodeoxyuridylate) than when bound to poly(deoxyadenlyate-deoxythymidylate). Quenching of 33258 Hoechst fluorescence can also be used to detect biosynthetic incorporation of 5-bromodeoxyuridine into the DNA of living cells. This property of 33258 Hoechst should allow fluorescence-activated cell and chromosome sorting according to the extent of DNA synthesis, providing a bridge between biochemical and cytologic analyses of processes related to DNA replication.


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