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Bridging fluorescence microscopy and electron microscopy

Development of new fluorescent probes and fluorescence microscopes has led to new ways to study cell biology. With the emergence of specialized microscopy units at most universities and research centers, the use of these techniques is well within reach for a broad research community. A major breakth...

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Detalles Bibliográficos
Autor principal: Giepmans, Ben N. G.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491700/
https://www.ncbi.nlm.nih.gov/pubmed/18575880
http://dx.doi.org/10.1007/s00418-008-0460-5
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author Giepmans, Ben N. G.
author_facet Giepmans, Ben N. G.
author_sort Giepmans, Ben N. G.
collection PubMed
description Development of new fluorescent probes and fluorescence microscopes has led to new ways to study cell biology. With the emergence of specialized microscopy units at most universities and research centers, the use of these techniques is well within reach for a broad research community. A major breakthrough in fluorescence microscopy in biology is the ability to follow specific targets on or in living cells, revealing dynamic localization and/or function of target molecules. One of the inherent limitations of fluorescence microscopy is the resolution. Several efforts are undertaken to overcome this limit. The traditional and most well-known way to achieve higher resolution imaging is by electron microscopy. Moreover, electron microscopy reveals organelles, membranes, macromolecules, and thus aids in the understanding of cellular complexity and localization of molecules of interest in relation to other structures. With the new probe development, a solid bridge between fluorescence microscopy and electron microscopy is being built, even leading to correlative imaging. This connection provides several benefits, both scientifically as well as practically. Here, I summarize recent developments in bridging microscopy.
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spelling pubmed-24917002008-07-31 Bridging fluorescence microscopy and electron microscopy Giepmans, Ben N. G. Histochem Cell Biol Review Development of new fluorescent probes and fluorescence microscopes has led to new ways to study cell biology. With the emergence of specialized microscopy units at most universities and research centers, the use of these techniques is well within reach for a broad research community. A major breakthrough in fluorescence microscopy in biology is the ability to follow specific targets on or in living cells, revealing dynamic localization and/or function of target molecules. One of the inherent limitations of fluorescence microscopy is the resolution. Several efforts are undertaken to overcome this limit. The traditional and most well-known way to achieve higher resolution imaging is by electron microscopy. Moreover, electron microscopy reveals organelles, membranes, macromolecules, and thus aids in the understanding of cellular complexity and localization of molecules of interest in relation to other structures. With the new probe development, a solid bridge between fluorescence microscopy and electron microscopy is being built, even leading to correlative imaging. This connection provides several benefits, both scientifically as well as practically. Here, I summarize recent developments in bridging microscopy. Springer-Verlag 2008-06-25 2008-08 /pmc/articles/PMC2491700/ /pubmed/18575880 http://dx.doi.org/10.1007/s00418-008-0460-5 Text en © Springer-Verlag 2008
spellingShingle Review
Giepmans, Ben N. G.
Bridging fluorescence microscopy and electron microscopy
title Bridging fluorescence microscopy and electron microscopy
title_full Bridging fluorescence microscopy and electron microscopy
title_fullStr Bridging fluorescence microscopy and electron microscopy
title_full_unstemmed Bridging fluorescence microscopy and electron microscopy
title_short Bridging fluorescence microscopy and electron microscopy
title_sort bridging fluorescence microscopy and electron microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491700/
https://www.ncbi.nlm.nih.gov/pubmed/18575880
http://dx.doi.org/10.1007/s00418-008-0460-5
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