scholarly journals Fluorescence imaging of chromosomal DNA using click chemistry

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Takumi Ishizuka ◽  
Hong Shan Liu ◽  
Kenichiro Ito ◽  
Yan Xu
Plant Methods ◽  
2018 ◽  
Vol 14 (1) ◽  
Author(s):  
Janet M. Paper ◽  
Thiya Mukherjee ◽  
Kathrin Schrick

RSC Advances ◽  
2019 ◽  
Vol 9 (44) ◽  
pp. 25318-25325
Author(s):  
Hanrui Li ◽  
Ke Li ◽  
Qi Zeng ◽  
Yun Zeng ◽  
Dan Chen ◽  
...  

Photo click chemistry has been used to prepare RGD conjugated silica nanoprobe (SiO2@T1-RGDk NPs) that exhibits excellent tumor targeting ability and negligible toxicity which enables them to be used for the diagnosis and treatment of cancer.


2014 ◽  
Vol 50 (89) ◽  
pp. 13746-13749 ◽  
Author(s):  
Jérémie Asselin ◽  
Carl Roy ◽  
Denis Boudreau ◽  
Younès Messaddeq ◽  
Rihab Bouchareb ◽  
...  

“Click” chemistry was used to functionalize silica substrates with pH-sensitive nanoparticles, thus producing uniform and highly luminescent ion-sensitive surfaces for quantitative and spatially-resolved extracellular measurements on live cells.


2020 ◽  
Vol 11 (2) ◽  
pp. 1684-1691
Author(s):  
Jingyi Zhou ◽  
Weicang Wang ◽  
Jianan Zhang ◽  
Zheyuan Du ◽  
Haixia Yang ◽  
...  

Using click chemistry-based fluorescence imaging, here we show that curcumin, a bioactive dietary compound with a thiol-reactive α,β-unsaturated carbonyl moiety, can covalently modify protein thiols in colon and liver tissues in mice.


2016 ◽  
Vol 7 (9) ◽  
pp. 6182-6189 ◽  
Author(s):  
Xiaoru Zhang ◽  
Ruijuan Li ◽  
Yuanyuan Chen ◽  
Shusheng Zhang ◽  
Wenshuang Wang ◽  
...  

We report herein imaging cell surface glycosylation by using click chemistry and DNA rolling circle amplification (RCA) to improve detection sensitivity..


2012 ◽  
Vol 177 (2) ◽  
pp. 344-348 ◽  
Author(s):  
Patrick J.M. Zessin ◽  
Kieran Finan ◽  
Mike Heilemann

Author(s):  
C J R Sheppard

The confocal microscope is now widely used in both biomedical and industrial applications for imaging, in three dimensions, objects with appreciable depth. There are now a range of different microscopes on the market, which have adopted a variety of different designs. The aim of this paper is to explore the effects on imaging performance of design parameters including the method of scanning, the type of detector, and the size and shape of the confocal aperture.It is becoming apparent that there is no such thing as an ideal confocal microscope: all systems have limitations and the best compromise depends on what the microscope is used for and how it is used. The most important compromise at present is between image quality and speed of scanning, which is particularly apparent when imaging with very weak signals. If great speed is not of importance, then the fundamental limitation for fluorescence imaging is the detection of sufficient numbers of photons before the fluorochrome bleaches.


Author(s):  
Byunghee Hwang ◽  
Tae-Il Kim ◽  
Hyunjin Kim ◽  
Sungjin Jeon ◽  
Yongdoo Choi ◽  
...  

A ubiquinone-BODIPY photosensitizer self-assembles into nanoparticles (PS-Q-NPs) and undergoes selective activation within the highly reductive intracellular environment of tumors, resulting in “turn-on” fluorescence and photosensitizing activities.


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