Styryl Dyes as Two-Photon Excited Fluorescent Probes for DNA Detection and Two-Photon Laser Scanning Fluorescence Microscopy of Living Cells

2010 ◽  
Vol 20 (4) ◽  
pp. 865-872 ◽  
Author(s):  
Valentyna P. Tokar ◽  
Mykhaylo Yu. Losytskyy ◽  
Tymish Y. Ohulchanskyy ◽  
Dmytro V. Kryvorotenko ◽  
Vladyslava B. Kovalska ◽  
...  
RSC Advances ◽  
2016 ◽  
Vol 6 (75) ◽  
pp. 70960-70971 ◽  
Author(s):  
Chun Zhang ◽  
Dan Wang ◽  
Li Zhang ◽  
Jing-Fu Guo ◽  
Ai-Min Ren

The two-photon fluorescent probes show dual signal for β-gal bio-imaging.


The Analyst ◽  
2018 ◽  
Vol 143 (23) ◽  
pp. 5799-5804 ◽  
Author(s):  
Wan Sun ◽  
Jing-Xue Cui ◽  
Le-Le Ma ◽  
Zhong-Lin Lu ◽  
Bing Gong ◽  
...  

TP-2Bz, as a nucleus targeting “D–π–A” molecule, was developed as a two-photon turn-on fluorescent probe for the viscosity and GQ DNA detection in cell nuclei.


2010 ◽  
Vol 12 (10) ◽  
pp. 2194-2197 ◽  
Author(s):  
Xin Jiang Feng ◽  
Po Lam Wu ◽  
Frédéric Bolze ◽  
Heidi W. C. Leung ◽  
King Fai Li ◽  
...  

1999 ◽  
Vol 5 (S2) ◽  
pp. 1060-1061
Author(s):  
J. M. Squirrell ◽  
D. L. Wokosin ◽  
B. D. Bavister ◽  
J. G. White

A major challenge for fluorescence imaging of living cells is maintaining viability during and following prolonged exposure to excitation illumination, especially when imaging over hours or even days, as when studying mammalian embryonic development. The use of specific fluorescently labeled components in living embryos promises to reveal the roles of organelles and molecules in a native and reproducible context. However, to gain a thorough understanding of dynamic biological systems, events of interest must be recorded as they occur, while limiting perturbations caused by the observation technique. Therefore, establishing long-term fluorescence imaging methods that maintain viability is critical for advancing our understanding of cell and developmental biology.One promising technique for imaging living cells is two photon laser scanning microscopy (TPLSM). The lower energy per photon and the restriction of fluorophore excitation to the imaged focal plane should reduce the total photodamage to thick specimens when compared to conventional laser scanning confocal microscopy (LSCM).


ACS Sensors ◽  
2020 ◽  
Vol 5 (4) ◽  
pp. 1068-1074
Author(s):  
Carlos Benitez-Martin ◽  
Juan A. Guadix ◽  
John R. Pearson ◽  
Francisco Najera ◽  
Jose M. Perez-Pomares ◽  
...  

Bioimaging ◽  
1996 ◽  
Vol 4 (3) ◽  
pp. 168-178 ◽  
Author(s):  
J D Bhawalkar ◽  
A Shih ◽  
S J Pan ◽  
W S Liou ◽  
J Swiatkiewicz ◽  
...  

2007 ◽  
Vol 467 (1) ◽  
pp. 325-338 ◽  
Author(s):  
V. M. Yashchuk ◽  
V. V. Gusak ◽  
I. M. Dmytruk ◽  
V. M. Prokopets ◽  
V. Yu. Kudrya ◽  
...  
Keyword(s):  

2015 ◽  
Vol 3 (16) ◽  
pp. 3315-3323 ◽  
Author(s):  
A. L. Capodilupo ◽  
V. Vergaro ◽  
E. Fabiano ◽  
Milena De Giorgi ◽  
F. Baldassarre ◽  
...  

Three fluorenone-based two-photon fluorescent probes for specific targeting of lysosomes and mitochondria in cancer cells.


RSC Advances ◽  
2017 ◽  
Vol 7 (27) ◽  
pp. 16730-16736 ◽  
Author(s):  
Ruiqing Feng ◽  
Longlong Li ◽  
Bing Li ◽  
Jinhui Li ◽  
Dan Peng ◽  
...  

We report two turn-on RNA probes that can light up endogenous RNA in the nucleoli and cytoplasm of living cells under a two-photon microscope.


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