Simple Method for Sub-Diffraction Resolution Imaging of Cellular Structures on Standard Confocal Microscopes by Three-Photon Absorption of Quantum Dots

• Anje Sporbert ,

  * E-mail: asporb@mdc-berlin.de (AS); darius.widera@uni-bielefeld.de (DW)

  Affiliation Confocal and 2-Photon Microscopy Core Facility, Max-Delbrueck-Center for Molecular Medicine Berlin, Berlin, Germany

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• Zoltan Cseresnyes,

  Affiliation Confocal and 2-Photon Microscopy Core Facility, Max-Delbrueck-Center for Molecular Medicine Berlin, Berlin, Germany

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• Meike Heidbreder,

  Affiliation Department of Biotechnology and Biophysics, Julius-Maximilians-Universität, Am Hubland, Würzburg, Germany

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• Petra Domaing,

  Affiliation Confocal and 2-Photon Microscopy Core Facility, Max-Delbrueck-Center for Molecular Medicine Berlin, Berlin, Germany

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• Stefan Hauser,

  Affiliation Molecular Neurobiology, University of Bielefeld, Bielefeld, Germany

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• Barbara Kaltschmidt,

  Affiliations Molecular Neurobiology, University of Bielefeld, Bielefeld, Germany, LiMiTec, Light Microscopy Technology Platform, University of Bielefeld, Bielefeld, Germany

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• Christian Kaltschmidt,

  Affiliations LiMiTec, Light Microscopy Technology Platform, University of Bielefeld, Bielefeld, Germany, Cell Biology, University of Bielefeld, Bielefeld, Germany

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• Mike Heilemann,

  Affiliation Physical and Theoretical Chemistry, Goethe-University Frankfurt, Frankfurt/Main, Germany

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• Darius Widera

  * E-mail: asporb@mdc-berlin.de (AS); darius.widera@uni-bielefeld.de (DW)

  Affiliations LiMiTec, Light Microscopy Technology Platform, University of Bielefeld, Bielefeld, Germany, Cell Biology, University of Bielefeld, Bielefeld, Germany

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