Gallery
From BioDIP
(Difference between revisions)
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=== Peter Evennett === | === Peter Evennett === | ||
− | ==== "Principles of Microscopy" course 2007 ==== | + | ==== "Principles of Light Microscopy" course 2007 ==== |
<gallery> | <gallery> | ||
Image:Course-poster.jpg | course announcement | Image:Course-poster.jpg | course announcement |
Revision as of 17:17, 7 September 2009
Contents |
Images acquired with our equipment
Effect of the CLSM pinhole
overview images
- Typical overview image of a tissue sample region. Pinhole diameter decreases from 8 airy units to 1 airy unit.
- Available as Video
- Invitrogen FluoCells(r) #4, Zeiss LSM 510, Plan-Apochromat 63x/1.4, 488 nm + 594 nm excitation, 505-580 nm + LP610 nm detection
XY
- High resolution image, acquired with decreasing pinhole diameter from 8 airy units to 0.6 airy units.
- Available as Video
- Invitrogen FluoCells(r) #4, Zeiss LSM 510, Plan-Apochromat 63x/1.4, 594 nm excitation, LP610 nm detection
XYZ
- One region of the sample was imaged with decreasing pinhole diameter, starting from 8 airy units (first image) down to 1 airy units (last image).
- Available as Video
- Invitrogen FluoCells(r) #4, Zeiss LSM 510, Plan-Apochromat 63x/1.4, 488 nm excitation, 505-580 nm detection, 0.2 µm Z-stepsize, Bitplane Imaris
Cleaning an objective makes sense
- Invitrogen FluoCells(r) #6, Zeiss LSM 510, Plan-Apochromat 63x/1.4, 488nm excitation, 505-550nm detection, pinhole @98µm