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High-speed microscopy of continuously moving cell culture vessels

We report a method of high-speed phase contrast and bright field microscopy which permits large cell culture vessels to be scanned at much higher speed (up to 30 times faster) than when conventional methods are used without compromising image quality. The object under investigation moves continuousl...

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Detalles Bibliográficos
Autores principales: Schenk, Friedrich Walter, Brill, Nicolai, Marx, Ulrich, Hardt, Daniel, König, Niels, Schmitt, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036042/
https://www.ncbi.nlm.nih.gov/pubmed/27667637
http://dx.doi.org/10.1038/srep34038
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author Schenk, Friedrich Walter
Brill, Nicolai
Marx, Ulrich
Hardt, Daniel
König, Niels
Schmitt, Robert
author_facet Schenk, Friedrich Walter
Brill, Nicolai
Marx, Ulrich
Hardt, Daniel
König, Niels
Schmitt, Robert
author_sort Schenk, Friedrich Walter
collection PubMed
description We report a method of high-speed phase contrast and bright field microscopy which permits large cell culture vessels to be scanned at much higher speed (up to 30 times faster) than when conventional methods are used without compromising image quality. The object under investigation moves continuously and is captured using a flash illumination which creates an exposure time short enough to prevent motion blur. During the scan the object always stays in focus due to a novel hardware-autofocus system.
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spelling pubmed-50360422016-09-30 High-speed microscopy of continuously moving cell culture vessels Schenk, Friedrich Walter Brill, Nicolai Marx, Ulrich Hardt, Daniel König, Niels Schmitt, Robert Sci Rep Article We report a method of high-speed phase contrast and bright field microscopy which permits large cell culture vessels to be scanned at much higher speed (up to 30 times faster) than when conventional methods are used without compromising image quality. The object under investigation moves continuously and is captured using a flash illumination which creates an exposure time short enough to prevent motion blur. During the scan the object always stays in focus due to a novel hardware-autofocus system. Nature Publishing Group 2016-09-26 /pmc/articles/PMC5036042/ /pubmed/27667637 http://dx.doi.org/10.1038/srep34038 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Schenk, Friedrich Walter
Brill, Nicolai
Marx, Ulrich
Hardt, Daniel
König, Niels
Schmitt, Robert
High-speed microscopy of continuously moving cell culture vessels
title High-speed microscopy of continuously moving cell culture vessels
title_full High-speed microscopy of continuously moving cell culture vessels
title_fullStr High-speed microscopy of continuously moving cell culture vessels
title_full_unstemmed High-speed microscopy of continuously moving cell culture vessels
title_short High-speed microscopy of continuously moving cell culture vessels
title_sort high-speed microscopy of continuously moving cell culture vessels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036042/
https://www.ncbi.nlm.nih.gov/pubmed/27667637
http://dx.doi.org/10.1038/srep34038
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