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Offers fast and sensitive 3D imaging, utilizing WF imaging, confocal imaging with 2 different pinhole sizes (40µm for higher contrast/25 µm for higher resolution), or TIRF (total internal reflection) imaging. |
Frequently Asked Questions:
How do I add and clean immersion on and off objectives correctly?
Proper Use of Objective Immersion Oil
Determining if you’ve used the right amount of oil
How do I choose the right excitation and emission settings for my fluorophore?
Find your fluorophore on FPbase. Based on the excitation and emission data, chose the closest filter set in the software.
Which objectives are installed in this system?
You can find the list at the end of this page, file “Objectivefinder_spinning disk.pdf“.
How do I save and access my data?
Save the data in:
→ open the driver data (D :) “Data_Bioimg”
→ open folder with your Weizmann user name
→ open a new folder with the date (crucial)
→ transfer the data (characters like ~!@#$%^&*()`;’:<>,/?[]{} are not allowed, and files including them are not copied)
Once you are done, the computer will synchronize the correctly saved data to the “bioimg” server.
To see the data on your PC, follow the instructions in this link: BioImg Storage Server system.
**When starting to work with the Bioimaging system for the first time, please make sure you have a UNIX ID added to your WIS ID (you can check it with your unit administrator)
How can I visualize the data on my pc?
You can open it in ImageJ
You can open it on one of our Image Analysis Software and Workstations
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Learn more: Microscopy: Optical Sectioning and Confocal Microscopy (Kurt Thorn) Complete Microscopy Training Course |
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405-445-488-514-561-633
450-525-600-647 *dichroic mirror deflects between GFP-RFP/CFP-YFP detection |
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