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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-5036042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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