Service
Confocal Microscopy can be used for the generation of confocal images of fixed samples and the investigation of living cells with advanced fluorescence techniques.
Confocal images:
- Pre-experimental consulting and hands-on training
- 2-dimensional confocal images
- Multi-channel images with up to 4 fluorophores
- Exact overlay with differential interference contrast (DIC) images
- Fluorescence intensity profiles
- Colocalization analysis
- 3-dimensional confocal images
- Preparation of image stacks („z-stacks“)
- Reconstruction of 3-dimensional objects
Advanced fluorescence techniques:
- Pre-experimental consulting and hands-on training
- FRAP (fluorescence recovery after photobleaching) and
- FLIP (fluorescence loss in photobleaching) to determine the mobility of fluorescently labelled molecules in living cells
- FRET (Förster resonance energy transfer) to detect interaction of fluorescently labeled molecules
- Use of photoconvertible and photoactivatable fluorescent proteins to determine protein dynamics in living cells
- Spectral imaging and linear unmixing for the separation of more than 4 fluorophores
- Single-molecule RNA fluorescence in situ hybridization (smRNA-FISH)
- Super-resolution microscopy based on single molecule localization such as dSTORM
- Live-cell imaging with temperature- and CO2-control