Fluorescence enhancement induced by the interaction of silver nanoclusters with lead ions in water

Author(s):  
L. Burratti ◽  
E. Ciotta ◽  
E. Bolli ◽  
S. Kaciulis ◽  
M. Casalboni ◽  
...  
2018 ◽  
Vol 10 (18) ◽  
pp. 2138-2143 ◽  
Author(s):  
Xu Li ◽  
Wenxiang Wang ◽  
Desong Yang ◽  
Jie Wu ◽  
Baihua Zhang ◽  
...  

Telomerase activity was detected based on primer extension-mediated fluorescence enhancement of silver nanoclusters.


The Analyst ◽  
2017 ◽  
Vol 142 (5) ◽  
pp. 800-807 ◽  
Author(s):  
Wei-Xian Wang ◽  
Yee-Wai Cheung ◽  
Roderick M. Dirkzwager ◽  
Wai-Chung Wong ◽  
Julian A. Tanner ◽  
...  

Nonspecific AgNCs-dsDNA combined with a specific aptamer are used to detect PfLDH with significant fluorescence enhancement and specific quenching.


2015 ◽  
Vol 7 (19) ◽  
pp. 7989-7994 ◽  
Author(s):  
Hui-Xia Han ◽  
Xue Tian ◽  
Xiang-Juan Kong ◽  
Ru-Qin Yu ◽  
Xia Chu

A label-free and turn-on strategy for H2O2 and glucose detection based on the cleavage of ssDNA by ˙OH and the fluorescence enhancement effect when guanine-rich (G-rich) DNA sequences are in proximity to DNA–silver nanoclusters (DNA–Ag NCs).


AIP Advances ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 125103
Author(s):  
Jing Chen ◽  
Yanqing Qiao ◽  
Yonghui Li ◽  
Tianyu Liu ◽  
Xiao-Dong Zhang

2019 ◽  
Author(s):  
Lukas P Smaga ◽  
Nicholas W Pino ◽  
Gabriela E Ibarra ◽  
Vishnu Krishnamurthy ◽  
Jefferson Chan

Controlled light-mediated delivery of biological analytes enables the investigation of highly reactivity molecules within cellular systems. As many biological effects are concentration dependent, it is critical to determine the location, time, and quantity of analyte donation. In this work, we have developed the first photoactivatable donor for formaldehyde (FA). Our optimized photoactivatable donor, photoFAD-3, is equipped with a fluorescence readout that enables monitoring of FA release with a concomitant 139-fold fluorescence enhancement. Tuning of photostability and cellular retention enabled quantification of intracellular FA release through cell lysate calibration. Application of photoFAD-3 uncovered the concentration range necessary for arresting wound healing in live cells. This marks the first report where a photoactivatable donor for any analyte has been used to quantify intracellular release.


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