Team:TU-Delft/Notebook/2013/07/08/

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3. Analysis of the Gel electrophoresis in lab meeting. pBAD and pT7 was not that good. AIP sender and receiver also shows contamination of wells. <br>
3. Analysis of the Gel electrophoresis in lab meeting. pBAD and pT7 was not that good. AIP sender and receiver also shows contamination of wells. <br>
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4. The biobricks: pBAD, pT7, GFP, AIP sender(Agr A: AgrC). AIP receiver(AgrB: AgrD), pTET:lysis were grown on Agar plates. But the negative control is not convincing, so Gel electrophoresis is run on random colonies from the plates to check. <br>
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Revision as of 11:05, 30 July 2013

Notebook

June
SunMonTueWedThuFriSat
1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18 19 20 21 22
23 24 25 26 27 28 29
30
July
SunMonTueWedThuFriSat
1 2 3 4 5 6
7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30 31










August
SunMonTueWedThuFriSat
1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30 31
September
SunMonTueWedThuFriSat
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30












4th of July


Lab work

1. Biobricks from the iGEM registry were streaked on Agar plates.
2. Transformation of the pTET backbone with Lysis cassette, which was done on 5/7/13.
3. Analysis of the Gel electrophoresis in lab meeting. pBAD and pT7 was not that good. AIP sender and receiver also shows contamination of wells.
4. The biobricks: pBAD, pT7, GFP, AIP sender(Agr A: AgrC). AIP receiver(AgrB: AgrD), pTET:lysis were grown on Agar plates. But the negative control is not convincing, so Gel electrophoresis is run on random colonies from the plates to check.