Team:TU-Delft/Notebook/2013/07/17/

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<p>  1. AIP receiver:GFP and pTET:RBS:cI was ligated and grown in Agar plates, then cultured, DNA extracted. <br>
<p>  1. AIP receiver:GFP and pTET:RBS:cI was ligated and grown in Agar plates, then cultured, DNA extracted. <br>
2. Running gel electrophoresis on the restriction digestion of AIP receiver:GFP  with XbaI +PstI and pTET:RBS:cI with EcoRI +SpeI. <br>
2. Running gel electrophoresis on the restriction digestion of AIP receiver:GFP  with XbaI +PstI and pTET:RBS:cI with EcoRI +SpeI. <br>
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2. Checking for Quick change on SUMO and Ulp 1, which was not successful at PCR Elongation temperature at 50 degree and 55 degree. <br>
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2. Checking for Quick change on SUMO and Ulp 1, which was not successful at PCR annealing temperature at 50 degree and 55 degree. <br>
3. Transformation of pT7(BBa_I719005) in DH5Alpha cells was carried out. <br>
3. Transformation of pT7(BBa_I719005) in DH5Alpha cells was carried out. <br>
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Latest revision as of 08:27, 4 October 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













17th of July


Lab work

1. AIP receiver:GFP and pTET:RBS:cI was ligated and grown in Agar plates, then cultured, DNA extracted.
2. Running gel electrophoresis on the restriction digestion of AIP receiver:GFP with XbaI +PstI and pTET:RBS:cI with EcoRI +SpeI.
2. Checking for Quick change on SUMO and Ulp 1, which was not successful at PCR annealing temperature at 50 degree and 55 degree.
3. Transformation of pT7(BBa_I719005) in DH5Alpha cells was carried out.