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From 2012.igem.org

Wednesday 09.05.12

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I have been playing around with a wiki design scheme today which can be found here. Hoping for some feedback this friday. Also I have been trying to make a calendar solution, but I haven't found any easier or more user-friendly way to implent this than to simply use the default wiki setup. So, at least for now, I think we should just keep using this site the way it is and add updates the way Gunvor did below (and I am doing now) ;) When you have added a new post to a day, you can click the button "Your signature with timestamp" in the editing menu to add your username along with the current time and date.

Hope you are all having a nice day and get to enjoy some sun!

--Oyas 09:45, 9 May 2012 (CDT)

Thursday 03.05.12

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We had a meeting, and we discussed several things we would like to look more into before we start planning what our genetic circuit will actually look like.

Here is a list of what we decided to do, and who will do it:

• Check Christopher Anderson's article to see how similar his project was to ours - Eirin
• Make a calendar on our wiki page - Ove
• Look deeper into what kind of anti cancer drugs we could make our cells synthetize - Nina
• Check if we have access to cancer cells, and find out more about molecules that are secreted form cancer cells in larger amounts than by normal cells - Gunvor
• Find out more about the O₂-sensitive promoter - Rahmi
• Rolf was also goint to do something, but I have forgotten what he was going to do...

- We also decided to have our next meeting at 13:30 next friday, and we decided to eat lunch together on wednesdays

- Rahmi came with a suggestion for characterization of the O₂-sensitive promoter:

We could make the promoter control the expression of a fluorescent protein, then transform the system to cells, grow the cells on a soft medium they could migrate into, let them grow for a while, and then investigate the medium for coloured cells.

Suggestion from Gunvor: We could use TIRF (Total Internal Reflection Fluorescence) microscope, which allows us to investigate the fluorescence in a certain layer of the medium.