3D Optical Sectioning Made Easy
20th & 21st March, University of Western Australia
Create optical sections of your fluorescent samples – free of scattered light. With structured illumination, you know that only the focal plane appears in your image: ApoTome.2 recognizes the magnification and moves the appropriate grid into the beampath. The system then calculates your optical section from three images with different grid positions without time lag. A reliable and trusted method for removal of scattered out-of-focus light, even in your thicker specimens. You get images with high contrast in the best possible resolution – simply brilliant optical sections.
Presentation
“Optical Sectioning Techniques Focussing on Widefield Structured Illumination”
Dr. Kyall Pocock, ZEISS Microscopy
Date: Tuesday 20th March
Time: 11:00 am – 12 pm
Location: Building M309, Level 2 presentation area
Please join us after the presentation for lunch and refreshments.
Hands-on Workshop – ApoTome.2
Date: Tuesday 20th March
Time: 1:00 – 2:30 pm and 3:00 – 4:30 pm
Date: Wednesday 21st March
Time: 9:30 – 11:00 am; 11:30 – 1:00 pm and 2:30 – 4:00 pm
Location: Building M309, Level 2 laboratory
Extra sessions available upon special request.
Venue Information
University of Western Australia
35 Stirling Highway, Crawley
Building M309, Level 2
University of Western Australia
35 Stirling Highway, Crawley
Building M309, Level 2
ApoTome.2 - Workshop Registration
Optical Sectioning Example
Widefield microscopy (left) comparison with optical sectioning (right).
ApoTome.2 - Highlights
- Outstanding ease of use – as simple as your routine fluorescence imaging
- Perfect images – with all magnifications
- Optimum results – free choice of light source and dyes
- Brilliant images – even with thick specimens