scholarly journals A multi-channel device for high-density target-selective stimulation and long-term monitoring of cells and subcellular features in C. elegans

Lab on a Chip ◽  
2014 ◽  
Vol 14 (23) ◽  
pp. 4513-4522 ◽  
Author(s):  
Hyewon Lee ◽  
Shin Ae Kim ◽  
Sean Coakley ◽  
Paula Mugno ◽  
Marc Hammarlund ◽  
...  

We present a high-density microfluidic device for target-selective illumination, selective stimulation, and long-term monitoring ofC. elegans.

2000 ◽  
Vol 175 ◽  
pp. 719-722
Author(s):  
P. Reig ◽  
I. Negueruela ◽  
M.J. Coe ◽  
J. Fabregat ◽  
A.E. Tarasov

AbstractWe present results of our long-term monitoring of LS I +61° 235 in the optical and infrared bands. This Be/X-ray binary exhibits V/R variability in the Hα line, which can be explained in the framework of the Global One-armed Oscillation model: a high density perturbation moves around inside the circumstellar disc of the Be star. The V>R and V<R peaks occur when the perturbation moves towards and away from the observer, respectively. In this work we show that the perturbation also affects the He I λ6678Å and Paschen lines. We also report on a correlation between the infrared emission and the V/R variability.


2014 ◽  
Vol 2014 ◽  
pp. 1-14 ◽  
Author(s):  
Hon Ming Yip ◽  
John C. S. Li ◽  
Kai Xie ◽  
Xin Cui ◽  
Agrim Prasad ◽  
...  

As microfluidics has been applied extensively in many cell and biochemical applications, monitoring the related processes is an important requirement. In this work, we design and fabricate a high-throughput microfluidic device which contains 32 microchambers to perform automated parallel microfluidic operations and monitoring on an automated stage of a microscope. Images are captured at multiple spots on the device during the operations for monitoring samples in microchambers in parallel; yet the device positions may vary at different time points throughout operations as the device moves back and forth on a motorized microscopic stage. Here, we report an image-based positioning strategy to realign the chamber position before every recording of microscopic image. We fabricate alignment marks at defined locations next to the chambers in the microfluidic device as reference positions. We also develop image processing algorithms to recognize the chamber positions in real-time, followed by realigning the chambers to their preset positions in the captured images. We perform experiments to validate and characterize the device functionality and the automated realignment operation. Together, this microfluidic realignment strategy can be a platform technology to achieve precise positioning of multiple chambers for general microfluidic applications requiring long-term parallel monitoring of cell and biochemical activities.


Oncotarget ◽  
2016 ◽  
Vol 7 (42) ◽  
pp. 67732-67747 ◽  
Author(s):  
Pilar Alvarez-Illera ◽  
Adolfo Sanchez-Blanco ◽  
Silvia Lopez-Burillo ◽  
Rosalba I. Fonteriz ◽  
Javier Alvarez ◽  
...  

Author(s):  
Barbara S. Minsker ◽  
Charles Davis ◽  
David Dougherty ◽  
Gus Williams

Kerntechnik ◽  
2018 ◽  
Vol 83 (6) ◽  
pp. 513-522 ◽  
Author(s):  
U. Hampel ◽  
A. Kratzsch ◽  
R. Rachamin ◽  
M. Wagner ◽  
S. Schmidt ◽  
...  

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