Team:NTNU-Trondheim/Notebook/October
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- | + | <li class='active'><a href='index.html'><span>Home</span></a></li> | |
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- | + | <li><a href='https://2013.igem.org/Team:NTNU-Trondheim/Project'><span>Project description</span></a></li> | |
- | + | <li><a href='https://2013.igem.org/Team:NTNU-Trondheim/novelapproach'><span>A novel approach</span></a></li> | |
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- | + | <li><a href='https://2013.igem.org/Team:NTNU-Trondheim/Experiments_and_Results'><span>Experiments and Results</span></a></li> | |
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- | + | <li class='last'><a href='https://2013.igem.org/Team:NTNU-Trondheim/Acknowledgements'><span>Acknowledgements</span></a></li> | |
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+ | <li class='has-sub'><a href='#'><span>Technical Stuff</span></a> | ||
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+ | <li><a href='https://2013.igem.org/Team:NTNU-Trondheim/Team'><span>Meet the team</span></a></li> | ||
+ | <li class='last'><a href='https://igem.org/Team.cgi?id=1082'><span>Official Team Profile</span></a></li> | ||
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+ | </ul> | ||
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+ | <li class='last'><a href='https://2012.igem.org/Team:NTNU_Trondheim/Matchmaker'><span>Matchmaker</span></a></li> | ||
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+ | <p style="text-align:center; color:black; ">SDS-PAGE of bacterial samples with the tat_GFP_RFP (ER1) and tat_ProteinG construct</p> </div> | ||
+ | <br><br> | ||
+ | <p>A new test on the Pm/XylS promoter was performed with the same conditions as earlier.<br></p> | ||
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+ | <p style="text-align:center; color:black; "> Wednesday 02 - Friday 04.10.2013</p> </div> | ||
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+ | <p> | ||
+ | As the first attempt to send in the tat_GFP_RFP construct to iGEM Headquarters failed, we redid the cloning as we did 26-28.09.2013 and sent in a new construct. | ||
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Latest revision as of 22:43, 4 October 2013
In order to determine if Protein G is produced in the S3-2B sample and wheater a GFP-RFP dimer is produced in the ER1 sample, a SDS-PAGE was performed. Liquid cell culture with ER1 (tat_GFP_RFP construct), S3-2B (tat_ProteinG construct) and wildtype ER2566 ''E.coli'' cells was centrifuged and the pallet was mixed with SDS loading buffer. This mix was then heated at 95 °C for 15 minutes. The SDS-PAGE results can be viewed in the figure below
Figure 1: SDS-PAGE of bacterial samples. From the left: wild type ER2566, tat_GFP_RFP and tat_ProteinG
A new test on the Pm/XylS promoter was performed with the same conditions as earlier.
As the first attempt to send in the tat_GFP_RFP construct to iGEM Headquarters failed, we redid the cloning as we did 26-28.09.2013 and sent in a new construct.