Optical Microscopy Unit (OM unit)
Optical Microscopy
- Altensteinstraße 23A, 14195 Berlin, Tel. 838 59145 |
Contact:
Dr. Katharina Achazi (katharina.achazi@fu-berlin.de)
Dr. Marta Maglione (m.maglione@fu-berlin.de)
Methods:
3D recontruction, Image analysis, Differential Interference Contrast Microscopy (DIC), Transmitted-light microscopy, Fluorescence microscopy, Fluorescence Recovery After Photobleaching (FRAP), Förster Resonance Energy Transfer (FRET), Histological Imaging with colour camera, High resolution microscopy, Confocal microscopy, Multichannel fluorescence imaging, Mosaic imaging, Multi Photon Microscopy (MPM), Phase contrast microscopy, Polarisation microscopy, Stimulated Emission Depletion (STED), Stochastic Optical Reconstruction Microscopy (STORM), Structured illuminationg, Total Internal Reflections Fluorescence Microscopy (TIRF), Time series with Temp. and CO2 control, Z Stacks
Devices:
Abberior STED Mikroskop (Expert Line), directly bookable, training mandatory, S2
Zeiss AiryScan (mit PicoQuant FLIM Modul), direkt buchbar, Training notwendig, S2
Nikon Eclipse Ti (with laser illumination), direkt buchbar, Training notwendig, S2
Leica SP8 (1), directly bookable, training mandatory, S2
Leica SP8 (2), directly bookable, training mandatory, S1
Leica SP5, directly bookable, training mandatory, S1 (assoc. AG Wiermer)
Bench Safe2020 (safety work bench), directly bookable, training mandatory, S2
Analyse PC (various analysis and presentation software), directly bookable
Services:
OM measurements, registration with OM is mandatory
Booking requirements:
Assisted and none-assisted usage of the equipment and of the OM-Service must register with the Optical Microscopy Unit (Register with Optical Microscopy Unit) including one-time approval by the group head.
Within the S1 and S2 areas proof of attendence at the anual S1 or S2 safety instruction is mandatory. More information is given on the Biolab Wiki.
Keywords
- 3D reconstruction
- CLSM - confocal laser scanning microscopy
- confocal microscopy
- DIC - differential interference contrast
- fluorescence microscopy
- FRAP - fluorescence recovery after photobleaching
- FRET - Förster-resonance energy transfer
- high resolution microscopy
- histological imaging
- image analysis
- mosaic imaging
- MPM - multi photon microscopy
- multi channel fluorescence imaging
- phase contrast microscopy
- polarisation microscopy
- STED - stimulated emission depletion
- STORM - stochastic optical reconstruction microscopy
- structured illumination
- time series microscopy (with temperature/CO2 control)
- TIRF - total internal reflection fluorescence microscopy
- transmitted light microscopy
- Z stacks