Team:Beijing Normal/Notebook

From 2008.igem.org

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(Dynamics)
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**9th September      We and Tsinghua team get together in our lab. We have a happy time together and share a lot.  
**9th September      We and Tsinghua team get together in our lab. We have a happy time together and share a lot.  
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**10th September    We provide Tsinghua Team with the cells harboring pSB1AC3 plasmids. We do the the tramsformation for them. Because they found their transformation effeciency is relatively low.
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**10th September    We provide Tsinghua Team with the cells harboring pSB1AC3 plasmids. We did the the tramsformation for them. Because they found their transformation effeciency is relatively low.
-
**17th September    Tsinghua Team told us that the vector that we provided proved to work well. We are all pretty happy about this positive result.
+
**17th September    Tsinghua Team told us that the vector that we provided proved to work well. We were all pretty happy about this positive result.
 +
 
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**3th October      We and Chiba Team had a happy conversation via googletalk today. We share all the success and frustrations in the process. And we exchange our opinion about promotor function measurement. They told us that they have used BBa_T9002 because their project uses quorum sensing and the part(T9002) was GFP producer controlled by 3OC6HSL Receiver Device.And their result is pretty satisfying.  

Revision as of 08:39, 3 October 2008

thum Home The Team The Project Parts Submitted to the Registry Modeling Notebook

Bnu.jpg

Dynamics

  • == Communications ==
    • 17th June Attend the Asian Workshop meeting.
    • 17th July Meet up with Tsinghua Team, and learn fron their experiences.
    • 25th July With Invitrogen.Co. Ltd and Tsinghua team to sign up a contract.
    • 27th July Have a discussion with Tsinghua team about the transformation efficiency.

We generalize some key words from the discussion:

1. Make sure the concentration of the plasmids from the biobrick is enough for transformation.

2. Keep a low temprature when enzyme digestion is performed

3. The transformation product are always incubated for more than 1h.


    • 9th September We and Tsinghua team get together in our lab. We have a happy time together and share a lot.
    • 10th September We provide Tsinghua Team with the cells harboring pSB1AC3 plasmids. We did the the tramsformation for them. Because they found their transformation effeciency is relatively low.
    • 17th September Tsinghua Team told us that the vector that we provided proved to work well. We were all pretty happy about this positive result.
    • 3th October We and Chiba Team had a happy conversation via googletalk today. We share all the success and frustrations in the process. And we exchange our opinion about promotor function measurement. They told us that they have used BBa_T9002 because their project uses quorum sensing and the part(T9002) was GFP producer controlled by 3OC6HSL Receiver Device.And their result is pretty satisfying.


July
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August
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September
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October
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