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  Novel red fluorophores with superior performance in STED microscopy.

Wurm, C. A., Kolmakov, K., Göttfert, F., Ta, H., Bossi, M. L., Schill, H., et al. (2012). Novel red fluorophores with superior performance in STED microscopy. Optical Nanoscopy, 1: 7. doi:10.1186/2192-2853-1-7.

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 Creators:
Wurm, C. A.1, Author           
Kolmakov, K.1, Author           
Göttfert, F., Author
Ta, H., Author
Bossi, M. L.1, Author           
Schill, H.1, Author           
Berning, S.1, Author           
Jakobs, S.2, Author           
Donnert, G.1, Author           
Belov, V. N.1, Author           
Hell, S. W.1, Author           
Affiliations:
1Department of NanoBiophotonics, MPI for biophysical chemistry, Max Planck Society, ou_578627              
2Research Group of Mitochondrial Structure and Dynamics, MPI for biophysical chemistry, Max Planck Society, ou_578566              

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Free keywords: Microscopy, Confocal, STED, Fluorescence, Rhodamines, Bioconjugation, Super-resolution, Nanoscopy, Stimulated emission depletion
 Abstract: In optical microscopy, most red-emitting dyes provide only moderate performance due to unspecific binding, poor labeling efficiency, and insufficient brightness. Here we report on four novel red fluororescent dyes, including the first phosphorylated dye, created by combining a rigidized rhodamine backbone with various polar groups. They exhibit large fluorescence quantum yields and improved NHS ester stability. While these fluorophores are highly suitable for fluorescence microscopy in general, they excel in stimulated emission depletion (STED) microscopy, providing < 25 nm spatial resolution in raw images of cells.

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Language(s): eng - English
 Dates: 2012-09-28
 Publication Status: Published online
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 Rev. Type: Peer
 Identifiers: DOI: 10.1186/2192-2853-1-7
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Title: Optical Nanoscopy
Source Genre: Journal
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Pages: 7 Volume / Issue: 1 Sequence Number: 7 Start / End Page: - Identifier: -