Difference between revisions of "20230515"
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Revision as of 13:01, 15 May 2023
Activation of WT problem:
- characterise the rotation spectrum by also rotating the BV-2 KO and WT cells after they have been treated with an activating agent: agent inducing inflammatory response
- we want to do this because BV-2 WT might already be activated when we rotate them and we might be getting rotational spectra of activated microglial cells
- we want to make sure that the change in spectra is not due to the activation but due to the disease (build up of fatty acids)
Morphology:
- Morten concludes that there is more variation in size in KO cells than the WT cells, which is as expected
- we needed to do the morphology tests to make sure that the rotation results are not due to increase in size due to activation of the cells
- to confirm that everything is alright in terms of cell's size, we need to do the activation tests and see if the potential change in size is due to the activation
- need to keep taking images of the cell lines before splitting them for Morten's analysis
Biological duplicates:
- have multiple cell cultures of the individual cell lines: for ex 3 flasks of KO and 3 flasks of WT, and do rotation on them to get better statistics
- this is something that we can do during the summer holidays
Improving experimental results:
- check whether adding the extra chemicals from the protocol change the results of the rotation
- be more precise with cell counting during the experiments - we need to know how many cells we put into the chamber
- do the cells rotate faster when they clump up? we do experiments to confirm that
Writing the report:
- Ørjan helping us with the article: 12th of June?
To do:
- give Latifa access to the cell lab
- send email to Ørjan
- ask Petter to thaw more cells (closer to July) - start culturing the cells from scratch
- ask Petter how many vials we have at HTH