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Team:TU-Delft/Notebook/2013/08/15/
From 2013.igem.org
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4. pConst was cut with S+P earlier, CIP treatment was carried out on it today, followed by PCR purification. <br> | 4. pConst was cut with S+P earlier, CIP treatment was carried out on it today, followed by PCR purification. <br> | ||
5. AgrAC-pP2-GFP-TT was run on gel and DNA was extracted from the gel. <br> | 5. AgrAC-pP2-GFP-TT was run on gel and DNA was extracted from the gel. <br> | ||
| + | 6. Ligation of pConst and AgrAC-pP2-GFP-TT was carried out again. <br> | ||
| + | 7. pT7 and lysis device was ligated and kept in water bath at 16°C. <br> | ||
</p> | </p> | ||
Revision as of 14:26, 19 August 2013
Notebook
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15th of August
Lab work
1.DNA extraction of BBConst-AgrAC-pP2-GFP-TT from colonies grown on 14/8/13.
2. Mass spectrometry was done on the peptide proteins. The UV absorbance and MS-Q Time of flight graphs were obtained to check the concentration of peptides.
3. Restriction digestion of RBS-TetR-TT, pTet-RBS and pBAD-AgrAC-TT-pP2 with S+P was carried out and kept in 37°C for 2 hours.
4. pConst was cut with S+P earlier, CIP treatment was carried out on it today, followed by PCR purification.
5. AgrAC-pP2-GFP-TT was run on gel and DNA was extracted from the gel.
6. Ligation of pConst and AgrAC-pP2-GFP-TT was carried out again.
7. pT7 and lysis device was ligated and kept in water bath at 16°C.
