Team:TU-Delft/Notebook/2013/08/19/

From 2013.igem.org

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<p> 1. Carried out colony PCR on pTET:RBS:cI and ran on gel. Colony 5 was selected and inoculated in LB Broth. <br>  
<p> 1. Carried out colony PCR on pTET:RBS:cI and ran on gel. Colony 5 was selected and inoculated in LB Broth. <br>  
2. Carried out colony PCR on His-SUMO peptides with correct primer for pET23B and ran on gel. This gel gave good results. <br>
2. Carried out colony PCR on His-SUMO peptides with correct primer for pET23B and ran on gel. This gel gave good results. <br>
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<img src="https://2013.igem.org/File:130819_ptet%2BcI.tif" height=300px>
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3. Transformation of pBAD:AgrAC:pP2 was done in XL1 Blue cells and plated on agar plates.  <br>
3. Transformation of pBAD:AgrAC:pP2 was done in XL1 Blue cells and plated on agar plates.  <br>
4. PCR purification of His-SUMO-Peptides was done. <br>
4. PCR purification of His-SUMO-Peptides was done. <br>
5. 10X TBE buffer was made and kept in stock. <br>
5. 10X TBE buffer was made and kept in stock. <br>
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Revision as of 12:48, 22 August 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












19th of August


Lab work

1. Carried out colony PCR on pTET:RBS:cI and ran on gel. Colony 5 was selected and inoculated in LB Broth.
2. Carried out colony PCR on His-SUMO peptides with correct primer for pET23B and ran on gel. This gel gave good results.
3. Transformation of pBAD:AgrAC:pP2 was done in XL1 Blue cells and plated on agar plates.
4. PCR purification of His-SUMO-Peptides was done.
5. 10X TBE buffer was made and kept in stock.