Cancer Research UK Edinburgh Centre Imaging Facilities
Light microscopy plays an important role within the CRUK Edinburgh Centre, allowing scientists to visualise biology as it happens on the scale from a single cell to whole tissues. We have a range of cutting edge instrumentation to cover our researchers imaging needs within the centre and also contribute towards collaborations throughout the University of Edinburgh.
Contact: Martin Lee
A bespoke multiphoton microscope was custom built in a joint venture between the CRUK Edinburgh Centre and The University of Edinburgh's Engineering department. Multiphoton microscopy excels at imaging within in-vivo tissue as it allows deeper imaging of fluorescence as well as visualisation of many cell and tissue components with label free imaging techniques.
The CRUK Edinburgh Centre is also involved in pushing new techniques and imaging methods in the field. Thanks to the unique design of our microscope we are particularly active in the area of vibrational imaging, a way to image drugs and cells without using fluorescent tags. Working alongside chemists from The University of Edinburgh, we have been imaging the uptake of anti-cancer drugs without bulky fluorescent markers attached. This is an exciting step allowing us to truly understand how drugs are taken up into tumours.
System details: Multiphoton Microscope
Body: Olympus FV1000 with mini scanhead, IX81 frame with automated stage
Objective: 25x 1.05 NA Water Immersion
Lasers: APE picoEMERALD 720nm-990nm 5ps, 1064nm 6ps
Detectors: 4 PMTs, 2 channel FLIM, Photodiode with Lock-in Amplifier for SRS
Additional: Equipped with anaesthetic vaporizer machine and incubated chamber for live imaging
Olympus FV1000 Confocal Microscope
Confocal imaging remains a gold standard in optical imaging for biologists, offering high resolution 3D images on both live and fixed cells. Our researchers use fluorescent staining to light up different parts of the cell that they are interested in and the confocal microscope allows them to see in high detail changes that are occurring within the cells themselves.
System Information: Olympus FV1000
Body: IX81 with automated stage
Objectives: 4x, 10x, 20x, 40x, 60x (oil), 20x (water), 40x (water)
Lasers: 6 lasers from 405nm-633nm
Detectors: 3 PMTs, 2 with Spectral detection
Additional: Equipped with anaesthetic vaporizer machine and incubated chamber for live imaging. SIM scanner for FRAP, FLIP and photo-activation.
Our high throughput microscope allows researchers to screen large libraries of compounds and assess the effects on hundreds of cells using an automated imaging platform. Equipped with an incubated chamber the system also allows for extended time course studies, measuring cell motility, cell viability and proliferation. The high content nature is coupled with powerful software solutions to pull out the relevant data from 1000s of individual cells
System: Olympus ScanR
Body: IX83 with automated incubated stage
Objectives: 4x, 10x, 20x, 40x,
Fluorescence: Metal Halide Lamp with DAPI, FITC, Cy3 and Texas Red Filters
Our widefield epifluorescent microscope allows quick and easy access to a simple to use but using high quality objective lenses. This allows our researchers to quickly asses their experimental setups before using other imaging platforms but also serves as an excellent imaging platform itself when imaging flat samples such as histology sections or single cell layers.
Objectives: 4x, 10x, 20x, 40x, 60x (oil)
Fluorescence: Metal Halide Lamp with DAPI, FITC and Texas Red Filters
Detectors: DP71 colour camera
(For support in building the microscope we would like to thank: Cancer Research UK (grant C157/A12753), The College of Medicine and Veterinary Medicine at the University of Edinburgh, The Medical Research Council Human Genetics Unit, the Caledonia Events Committee (CRUK grant C157/A16508), and the Clerk Maxwell Cancer Fund. This work was supported by Cancer Research UK (program grant C157/A15703) and the European Research Council Advanced Investigator Grant (grant number 294440 Cancer Innovation to MCF).)