File:Single YFP molecule superresolution microscopy.png
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DescriptionSingle YFP molecule superresolution microscopy.png |
English: Superresolution Microscopy/ Optical nanoscopy using SPDMphymod as a new localization microscopy technique for standard fluorescent dyes
SPDMphymod image of protein distribution in a human cancer cell. Enlarged inserts above and below: Positions of single fluorescent molecules in Gaussian intensity shape of 5 nm standard deviation. Typical distance measurements in the 15 nm range are highlighted Fundamental to SPDMphymod are blinking phenomena (flashes of fluorescence), induced by reversible bleaches (metastable dark states). Individual molecules of the same spectral emission color can be detected. Counting individual molecules up to a density of 1000/µm2 – at present, this is possible in an area of up to 5000 µm2. Christoph Cremer, emeritus at Heidelberg university [1] Basic publications: Lemmer P, Gunkel M, Baddeley D, Kaufmann R, Urich A, Weiland Y, Reymann J, Müller P, Hausmann M, Cremer C: SPDM – Light Microscopy with Single Molecule Resolution at the Nanoscale. In: Applied Physics B 2008; 93: 1–12 Manuel Gunkel, Fabian Erdel, Karsten Rippe, Paul Lemmer, Rainer Kaufmann, Christoph Hörmann, Roman Amberger and Christoph Cremer: Dual color localization microscopy of cellular nanostructures. In: Biotechnology Journal, 2009, 4, 927-938. ISSN 1860-6768 |
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Source | Own work | ||
Author | Andy Nestl | ||
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Gallery edit
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Breast Cancer Cells: 3D Dual Color Super Resolution Microscopy of Her2 and Her3 & cluster calculations
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Single YFP molecule detection in a human cancer cell. Typical distance measurements 15 nm
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Co- localisation microscopy with GFP and RFP fusion proteins (nucleus of a bone cancer cell) 120.000 localized molecules in a widefield area(470 µm2)
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Label-free Localisation Microscopy SPDM - Super Resolution Microscopy reveals prior undetebable intracellular structures
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Investigation of human eye tissue, affected by macular degeneration AMD
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Virus Super Resolution Microscopy SPDM Cremer/Wege labs
Licensing edit
Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the section entitled GNU Free Documentation License.http://www.gnu.org/copyleft/fdl.htmlGFDLGNU Free Documentation Licensetruetrue |
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Original upload log edit
This image was originally uploaded in BMP format as File:Single_YFP_molecule_superresolution_microscopy.tif. The original upload history (excluding reverts) is shown below:
- 2009-12-01T12:00:38Z Andy Nestl 340x686 (699774 Bytes, image/x-bmp) test2
- 2009-12-01T11:45:07Z Andy Nestl 340x686 (700634 Bytes, image/tiff) {{Information |Description={{en|1=Superresolution Microscopy using SPDMphymod as a new localization microscopy technique for standard fluorescent dyes}} |Source={{own}} |Author=Andy Nestl |Date=2009-12-01 |Permission=given by Christoph
- ↑ https://www.physik.uni-heidelberg.de/personen/lsf.php?details=1537 |titel=Fakultät für Physik und Astronomie |abruf=2020-10-01
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- File:3D Dual Color Super Resolution Microscopy Cremer 2010.png
- File:GFP Superresolution Christoph Cremer.JPG
- File:Label-free Localisation Microscopy SPDM - Super Resolution Microscopy Christoph Cremer.jpg
- File:Opthalmology AMD Super Resolution Cremer.png
- File:Single YFP molecule superresolution microscopy-ru.png
- File:Single YFP molecule superresolution microscopy.png
- File:TMV virus super resolution microscopy Christoph Cremer Christina Wege.jpg
- Template:Other versions/Single YFP molecule superresolution microscopy
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