Team:NTNU-Trondheim/Notebook/October
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- | 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. | + | <p style="text-align:center; color:black; "> Wednesday 02.10.2013</p> </div> |
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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> | ||
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+ | <p>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 | 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 | ||
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<div class="col4" style="background-color:white;><a href="https://static.igem.org/mediawiki/2013/f/f9/Vesicles_trial_1.jpg"> <img src="https://static.igem.org/mediawiki/2013/f/f9/Vesicles_trial_1.jpg" width="303"> | <div class="col4" style="background-color:white;><a href="https://static.igem.org/mediawiki/2013/f/f9/Vesicles_trial_1.jpg"> <img src="https://static.igem.org/mediawiki/2013/f/f9/Vesicles_trial_1.jpg" width="303"> | ||
<p style="text-align:center; color:black; "> Figure 1.</p> </div> | <p style="text-align:center; color:black; "> Figure 1.</p> </div> |
Revision as of 08:36, 4 October 2013
Wednesday 02.10.2013
SDS-PAGE of bacterial samples with the tat_GFP_RFP (ER1) and tat_ProteinG construct
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.