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Two-color live-cell STED nanoscopy by click labeling with cell-permeable fluorophores
View ORCID ProfileCarola Gregor, View ORCID ProfileFlorian Grimm, View ORCID ProfileJasmin Rehman, View ORCID ProfileChristian A. Wurm, View ORCID ProfileAlexander Egner
doi: https://doi.org/10.1101/2022.09.11.507450
Carola Gregor
1Department of Optical Nanoscopy, Institut für Nanophotonik Göttingen e.V., Göttingen, Germany
2Cluster of Excellence “Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells” (MBExC), University of Göttingen, Göttingen, Germany
Florian Grimm
3Abberior GmbH, Hans-Adolf-Krebs Weg 1, 37077 Göttingen, Germany
Jasmin Rehman
3Abberior GmbH, Hans-Adolf-Krebs Weg 1, 37077 Göttingen, Germany
Christian A. Wurm
3Abberior GmbH, Hans-Adolf-Krebs Weg 1, 37077 Göttingen, Germany
Alexander Egner
1Department of Optical Nanoscopy, Institut für Nanophotonik Göttingen e.V., Göttingen, Germany
2Cluster of Excellence “Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells” (MBExC), University of Göttingen, Göttingen, Germany
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Posted September 13, 2022.
Two-color live-cell STED nanoscopy by click labeling with cell-permeable fluorophores
Carola Gregor, Florian Grimm, Jasmin Rehman, Christian A. Wurm, Alexander Egner
bioRxiv 2022.09.11.507450; doi: https://doi.org/10.1101/2022.09.11.507450
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