scholarly journals M13 Virus‐Based Framework for High Fluorescence Enhancement

Small ◽  
2019 ◽  
Vol 15 (28) ◽  
pp. 1901233 ◽  
Author(s):  
Shengnan Huang ◽  
Jifa Qi ◽  
Dane W. deQuilettes ◽  
Mantao Huang ◽  
Ching‐Wei Lin ◽  
...  
Nanoscale ◽  
2019 ◽  
Vol 11 (30) ◽  
pp. 14322-14329 ◽  
Author(s):  
Baosheng Du ◽  
Chengchun Tang ◽  
Dan Zhao ◽  
Hong Zhang ◽  
Dengfeng Yu ◽  
...  

High fluorescence enhancement has been realized by optimizing the evanescent field of ZnO nanorods.


2010 ◽  
Vol 114 (49) ◽  
pp. 21142-21149 ◽  
Author(s):  
Henryk Szmacinski ◽  
Ramachandram Badugu ◽  
Joseph R. Lakowicz

2015 ◽  
Vol 7 (1) ◽  
pp. 40-44 ◽  
Author(s):  
Kang Mao ◽  
Yizhen Liu ◽  
Huaming Xiao ◽  
Yinran Chen ◽  
Zitong Wu ◽  
...  

For the first time, gold nanoclusters were found to exhibit high fluorescence enhancement ability based on the metal-enhanced fluorescence (MEF) effect, which can effectively enhance the fluorescence of fluorescein isothiocyanate (FITC).


2012 ◽  
Vol 441 ◽  
pp. 398-402
Author(s):  
Tong Wu ◽  
Xiao Jun Peng

The synthesis and characteristics of a new styryl colorific and fluorescent dual signal probe for DNA are described. Sty-HPy shows a high fluorescence enhancement (> 35-fold) in conjunction with a visible colorific change (45 nm red-shift) when bound to dsDNA. The large Stokes shift (140 nm) and sensitive colorific response to DNA are both attributed to the rational design of intramolecular charge transfer (ICT) intra Sty-HPy.


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.


Sign in / Sign up

Export Citation Format

Share Document