A high-throughput method to quantify shape differences for three-dimensional imaging technologies

2006 ◽  
Vol 39 ◽  
pp. S651
Author(s):  
E. Kristensen ◽  
T.E. Parsons ◽  
B. Hallgrimsson ◽  
S. Boyd
2009 ◽  
Vol 149 (3) ◽  
pp. 1452-1461 ◽  
Author(s):  
Bernhard Biskup ◽  
Hanno Scharr ◽  
Andreas Fischbach ◽  
Anika Wiese-Klinkenberg ◽  
Ulrich Schurr ◽  
...  

Optica ◽  
2019 ◽  
Vol 6 (10) ◽  
pp. 1297 ◽  
Author(s):  
Yuanyuan Han ◽  
Rui Tang ◽  
Yi Gu ◽  
Alex Ce Zhang ◽  
Wei Cai ◽  
...  

Lab on a Chip ◽  
2012 ◽  
Vol 12 (15) ◽  
pp. 2630 ◽  
Author(s):  
Gregory G. Lewis ◽  
Matthew J. DiTucci ◽  
Matthew S. Baker ◽  
Scott T. Phillips

Author(s):  
Gency Gunasingh ◽  
Alexander Browning ◽  
Nikolas Haass

Tumour spheroids are fast becoming commonplace in basic cancer research and drug development. Obtaining high-quality data relating to the inner structure of spheroids is important for analysis, yet existing techniques often use equipment that is not commonly available, are expensive, laborious, cause significant size distortion, or are limited to relatively small spheroids. We present a high-throughput method of mounting, clearing, and imaging tumour spheroids that causes minimal size distortion. Spheroids are mounted in an agarose gel to prevent movement, cleared using a solution prepared from commonly available materials, and imaged using confocal microscopy. We find that our method yields high quality two- and three-dimensional images that provide information about the inner structure of spheroids.


2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Maria A. Guzman Aparicio ◽  
Teresa C. Chen

2018 ◽  
Author(s):  
Savannah L. Logan ◽  
Christopher Dudley ◽  
Ryan P. Baker ◽  
Michael J. Taormina ◽  
Edouard A. Hay ◽  
...  

ABSTRACTLight sheet fluorescence microscopy enables fast, minimally phototoxic, three-dimensional imaging of live specimens, but is currently limited by low throughput and tedious sample preparation. Here, we describe an automated high-throughput light sheet fluorescence microscope in which specimens are positioned by and imaged within a fluidic system integrated with the sheet excitation and detection optics. We demonstrate the ability of the instrument to rapidly examine live specimens with minimal manual intervention by imaging fluorescent neutrophils over a nearly 0.3 mm3 volume in dozens of larval zebrafish. In addition to revealing considerable inter-individual variability in neutrophil number, known previously from labor-intensive methods, three-dimensional imaging allows assessment of the correlation between the bulk measure of total cellular fluorescence and the spatially resolved measure of actual neutrophil number per animal. We suggest that our simple experimental design should considerably expand the scope and impact of light sheet imaging in the life sciences.


2016 ◽  
Vol 10 (1) ◽  
pp. 24-45 ◽  
Author(s):  
Laura Teodori ◽  
Annunziata Crupi ◽  
Alessandra Costa ◽  
Alberto Diaspro ◽  
Susanne Melzer ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document