scholarly journals Live Tissue Imaging Sheds Light on Cell Level Events During Ectodermal Organ Development

2020 ◽  
Vol 11 ◽  
Author(s):  
Isabel Mogollón ◽  
Laura Ahtiainen
2021 ◽  
Vol 28 (4) ◽  
pp. 603-622
Author(s):  
Qiang Huang ◽  
Aliesha Garrett ◽  
Shree Bose ◽  
Stephanie Blocker ◽  
Anne C. Rios ◽  
...  

PLoS ONE ◽  
2011 ◽  
Vol 6 (5) ◽  
pp. e20013 ◽  
Author(s):  
Alexander Venn ◽  
Eric Tambutté ◽  
Michael Holcomb ◽  
Denis Allemand ◽  
Sylvie Tambutté

2007 ◽  
pp. 79-85
Author(s):  
Marshall H. Montrose ◽  
Alastair J. M. Watson

2011 ◽  
Vol 16 (11) ◽  
pp. 116009 ◽  
Author(s):  
Jiun-Yann Yu ◽  
Chun-Hung Kuo ◽  
Daniel B. Holland ◽  
Yenyu Chen ◽  
Mingxing Ouyang ◽  
...  

BioTechniques ◽  
2021 ◽  
Author(s):  
Prajakta Deshpande ◽  
Neha Gogia ◽  
Anuradha Venkatakrishnan Chimata ◽  
Amit Singh

Numerous imaging modules are utilized to study changes that occur during cellular processes. Besides qualitative (immunohistochemical) or semiquantitative (Western blot) approaches, direct quantitation method(s) for detecting and analyzing signal intensities for disease(s) biomarkers are lacking. Thus, there is a need to develop method(s) to quantitate specific signals and eliminate noise during live tissue imaging. An increase in reactive oxygen species (ROS) such as superoxide (O2•-) radicals results in oxidative damage of biomolecules, which leads to oxidative stress. This can be detected by dihydroethidium staining in live tissue(s), which does not rely on fixation and helps prevent stress on tissues. However, the signal-to-noise ratio is reduced in live tissue staining. We employ the Drosophila eye model of Alzheimer's disease as a proof of concept to quantitate ROS in live tissue by adapting an unbiased method. The method presented here has a potential application for other live tissue fluorescent images.


2016 ◽  
Vol 6 (1) ◽  
pp. 285-292 ◽  
Author(s):  
Nicole Y.C. Yu ◽  
Connor A. O'Brien ◽  
Iveta Slapetova ◽  
Renee M. Whan ◽  
Melissa L. Knothe Tate

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