ApoTome2 Quick Guide PDF
ApoTome2 Quick Guide PDF
ApoTome2 Quick Guide PDF
1),
wait until TFT fully load
Press
on TFT again for objective back to
working position
2.
3.
4.
5.
8.
Notes:
2.
3.
4.
1.
Microscope Operation
1.
8. For Optical Sectioning with ApoTome, move ApoTome slider in manually and set optimum parameter for imaging
capturing under ApoTome Tab before go to Live to preview and proceed with exposure time adjustment and Snap
followed by Min/ Max for every single Channel
5. Go to Live to preview the sample (focus on your sample and do necessary adjustment to achieve best image)
Notes:
ApoTome Settings
Click Gallery to view all the slices capture with Show Dimension Labels for thickness details
6.
5.
Using focus drive of the microscope to focus on the highest position of the specimen. Click on Set First button to set the highest
position of the Z-stack. Focus in different direction to the lowest position of specimen. Click on the Set Last button to set the
lowest position. Click again on Live button to stop specimen scanning (prevent specimen from bleaching).
3.
Click on the number of slice thickness after Optimal to optimize number of slices to match the optimal Z-interval to the stack
size. Under Optimize Sectioning and step section, choose Optimal button to match the optical section from each channel.
2.
4.
1.
1. For 3D Projection, click 3D on the left panel of the Image with various option for 3D view
3D Projection
2.
Go to File, Save or Save as, select the folder and Save type
1.
To Save Images