This laser-scanning confocal microscope combines a pulsed white-light laser (440–790 nm), five high-sensitivity photon-counting detectors, and three STED depletion lasers for advanced confocal, super-resolution, and fluorescence lifetime imaging. The system supports both fixed-sample and live-cell applications, with environmental control for temperature and 5% CO₂.
- Laser-scanning confocal microscopy
- Multichannel STED and Tau-STED super-resolution imaging
- Fluorescence recovery after photobleaching (FRAP)
- Fluorescence lifetime imaging microscopy (FLIM)
- Fluorescence correlation spectroscopy (FCS)
- FLIM-FRET
- Lamda scanning (Ex and Em) and Spectral unmixing
- Live-cell imaging with temperature and 5% CO₂ control
Microscope Stand
- Leica DMi8 Inverted Microscope with Adaptive Focus Control (AFC)
- Scanning motorized stage and Z-Piezo stage with 500um travel (WieneckeSinske WSBPiezo)
Objectives:
- HC PL APO 10x/0.4 NA CS2
- HC PL APO 20x/0.75 NA CS2
- HC PL APO 40x/1.30 Oil CS2
- HC PL APO 86x/1.20 W motCORR STED W
- PHC PL APO 100x/1.40 OIL STED W
Available upon request - HC FLUOTAR L 25x/0.95 W VISIR
- HC PL APO 93x/1.30 GLYC motC STED W
- HC PL APO 40x/0.95 CORR
Light Sources:
- LED 3 broadband (390-680nm) with 3mm LLG for widefield
- White LED for transmitted light/DIC
Confocal module
- 8kHz Tandem Scanner STELLARIS 8 (galvo and resonant)
- HyD detectors:
- HyD S (pos 1 and pos 3)
- HyD X (pos 2 and pos 4)
- HyD R (pos 5)
Lasers
- 405nm CW laser
- 440-790nm White Light Laser (pulsed 10 to 80Hz)
- 592 nm STED depletion laser
- 660 nm STED depletion laser
- 775 nm STED depletion laser
Location
Weill Institute for Neurosciences Building (MB)
Room
451J
Core
Innovation Core (Weill)
Technique
Brightfield, DIC, phase
Confocal
FLIM
FRAP/Photoactivation
Inverted microscope
Live Cell
Spectral imaging
Super-resolution
Staff contact
Special Access requirements
Laser Safety
Training by Core Staff