Live cell imaging based on surface plasmon-enhanced fluorescence microscopy using random nanostructures

2014 ◽  
Author(s):  
Youngjin Oh ◽  
Wonju Lee ◽  
Taehwang Son ◽  
Sook Young Kim ◽  
Jeon-Soo Shin ◽  
...  
Author(s):  
Karla Balaa ◽  
Viviane Devauges ◽  
Yannick Goulam ◽  
Vincent Studer ◽  
Sandrine Lévêque-Fort ◽  
...  

2009 ◽  
Author(s):  
Karla Balaa ◽  
Viviane Devauges ◽  
Yannick Goulam ◽  
Vincent Studer ◽  
Sandrine Lévêque-Fort ◽  
...  

2011 ◽  
Vol 36 (16) ◽  
pp. 3051 ◽  
Author(s):  
Thomas Barroca ◽  
Karla Balaa ◽  
Julie Delahaye ◽  
Sandrine Lévêque-Fort ◽  
Emmanuel Fort

The Analyst ◽  
2018 ◽  
Vol 143 (22) ◽  
pp. 5559-5567 ◽  
Author(s):  
Thomas Söllradl ◽  
Kevin Chabot ◽  
Ulrike Fröhlich ◽  
Michael Canva ◽  
Paul G. Charette ◽  
...  

Validation of a combined metal-clad waveguide and surface enhanced fluorescence imaging platform for live cell imaging.


2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Dulanthi Weerasekera ◽  
Jonas Hahn ◽  
Martin Herrmann ◽  
Andreas Burkovski

Abstract Objectives In frame of a study to characterize the interaction of human macrophage-like cells with pathogenic corynebacteria, Corynebacterium diphtheriae and Corynebacterium ulcerans, live cell imaging experiments were carried out and time lapse fluorescence microscopy videos were generated, which are presented here. Data description The time lapse fluorescence microscopy data revealed new insights in the interaction of corynebacteria with human macrophage-like THP-1 cells. In contrast to uninfected cells and infections with non-pathogenic C. glutamicum used as a control, pathogenic C. diphtheriae and C. ulcerans showed highly detrimental effects towards human cells and induction of cell death of macrophages.


The Analyst ◽  
2014 ◽  
Vol 139 (22) ◽  
pp. 5954-5963 ◽  
Author(s):  
Weili Chen ◽  
Kenneth D. Long ◽  
Hojeong Yu ◽  
Yafang Tan ◽  
Ji Sun Choi ◽  
...  

Photonic crystal enhanced fluorescence microscopy can provide information about the spatial distribution of cell–surface interactions at the single-cell level.


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