Core Facility Unit (CFU)

Head Dr. Ralf Palmisano

Methods

  • Super-Resolution STED microscopy

  • Super-Resolution RESOLFT microscopy

  • Spinning-disc high speed (temporal) laser scanning live imaging microscopy

  • Fast multi-channel fluorescence microscopy

  • Multi-channel confocal microscopy with flexible spectral detection

  • Fluorescence recovery after photobleaching (FRAP)

  • Fluorescence resonance energy transfer (FRET)

  • Photoactivation

  • Spectral unmixing of fluorescent dyes

  • Deconvolution

  • Particle tracking and co-localisation

  • Environmental control chambers for live cell imaging

  • Fixation, Immunocytochemistry, sample preparation

  • Protein labeling and GFP fusions

  • Image processing

Fur any further question, please contact us. We will make it feasible!

In near future there will also be two high-end off-line workstations equipped with manufacturers offline licences and third party solutions, like OME, Huygens Deconvolution software and Fiji imaging tools.