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Microscope Name | Upright or Inverted? | Laser Lines | 37°C Incubation | Features | Recommended Techniques |
---|---|---|---|---|---|
SPE | Upright | 405, 488, 532, 640 | Possible |
| 3D imaging of fixed specimens on slides. Orthogonal scans (in XZ) using the Z Galvo. Live imaging of perfused specimens if an upright configuration is needed. |
SPE2 | Upright | 405, 488, 532, 640 | Possible |
| 3D imaging of fixed specimens on slides. Orthogonal scans (in XZ) using the Z Galvo. Live imaging of specimens in dishes possible with water dipping lenses using Oko-lab stage adapter if an upright configuration is needed. |
SPE3 | Inverted | 405, 488, 561, 640 | No |
| 3D imaging of specimens on slides and in dishes with multi-position acquisition and tiling. In comparison to other SPE confocal microscopes the 561 nm laser is closer to the excitation peak of most popular red fluorophores. Fluorescence and DIC on gridded 35 mm dishes for correlative light and electron microscopy. Matrix Screener software is available for high content screening type applications. |
SP5 | Inverted | 405, 457, 476, 488, 495, 561, 594, 633 | Yes |
| 3D imaging of specimens on slides and live imaging of specimens in 35 mm dishes and Lab-Tek chambered coverslips using Pe-Con incubation equipment. Multi-position acquisition and tiling. Fluorescence recovery after photobleaching (FRAP). Förster Resonance Energy Transfer by Acceptor Photobleaching or Sensitised Emission using FRET wizards. Fluorescence and DIC on gridded 35 mm dishes for correlative light and electron microscopy. Advanced experiment design using Live Data Mode (e.g. reconfiguring acquisition for SRRF). Matrix Screener for high content screening, export of data as OME TIFF. |
Olympus FV1200 | Inverted | 405, 458, 488, 515, 559, 635 Sim Scanner: 405 (pulsed), 440 | Yes |
| 3D scanning of fixed specimens. Live imaging of specimens in 35 mm dishes and chambered coverslips. Highly sensitivite live imaging of green and red fluorophores using the GaAsP detectors. Imaging of thick living specimens using the silicon lenses to correct for the refractive index of cytoplasm. Tiling of large specimens using the motorised stage. Ablation of cytoskeletal cortex in adherent cells using the pulsed 405 nm laser. Fluorescence and DIC on gridded 35 mm dishes for correlative light and electron microscopy. |
Radiance | Upright | 458, 488, 514, 543, 635 | Possible |
| 3D imaging of fixed specimens on slides. Other microscopes are recommended for live imaging of mammalian specimens and for more sophisticated FRAP capability. |
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