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Team:KULeuven/NotebookDaily
From 2011.igem.org
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<span class="notebook-header"><img src="http://www.shbts.nl/igem/images/notebook_top_wetlab_breed.png"</span><br> | <span class="notebook-header"><img src="http://www.shbts.nl/igem/images/notebook_top_wetlab_breed.png"</span><br> | ||
| - | <span class="notebook-dayno"> | + | <span class="notebook-dayno">4th of July</span><br> |
<span class="notebook-txt">The first week in the wet lab started with the preparation of materials needed in future experiments. We made growth medium and agar plates containing antibiotics, which will be used to culture bacteria. Furthermore competent cells were prepared with the CaCl2 – method. We also resuspended the DNA of the biobricks necessary for our project as described in the iGEM guidelines. We managed to perform the first transformations with the competent cells and the resuspended DNA and thus concluded that the competent cells were functional.</span><hr class="notebook-divider"> | <span class="notebook-txt">The first week in the wet lab started with the preparation of materials needed in future experiments. We made growth medium and agar plates containing antibiotics, which will be used to culture bacteria. Furthermore competent cells were prepared with the CaCl2 – method. We also resuspended the DNA of the biobricks necessary for our project as described in the iGEM guidelines. We managed to perform the first transformations with the competent cells and the resuspended DNA and thus concluded that the competent cells were functional.</span><hr class="notebook-divider"> | ||
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<span class="notebook-header"><img src="http://www.shbts.nl/igem/images/notebook_top_models_breed.png"</span><br> | <span class="notebook-header"><img src="http://www.shbts.nl/igem/images/notebook_top_models_breed.png"</span><br> | ||
| - | <span class="notebook-dayno"> | + | <span class="notebook-dayno">4th of July</span><br> |
<span class="notebook-txt">We installed the Matlab software and Simbiology toolkit, we watched some tutorial ‘webinars’ from Mathworks. In a meeting with the advisors, we learned more about the purpose and basics of modeling in synthetic biology. After downloading the projects of previous year teams of the KUleuven to understand the inner workings of their model.</span><hr class="notebook-divider"> | <span class="notebook-txt">We installed the Matlab software and Simbiology toolkit, we watched some tutorial ‘webinars’ from Mathworks. In a meeting with the advisors, we learned more about the purpose and basics of modeling in synthetic biology. After downloading the projects of previous year teams of the KUleuven to understand the inner workings of their model.</span><hr class="notebook-divider"> | ||
Revision as of 19:11, 27 July 2011
4th of July
The first week in the wet lab started with the preparation of materials needed in future experiments. We made growth medium and agar plates containing antibiotics, which will be used to culture bacteria. Furthermore competent cells were prepared with the CaCl2 – method. We also resuspended the DNA of the biobricks necessary for our project as described in the iGEM guidelines. We managed to perform the first transformations with the competent cells and the resuspended DNA and thus concluded that the competent cells were functional.
4th of July
We installed the Matlab software and Simbiology toolkit, we watched some tutorial ‘webinars’ from Mathworks. In a meeting with the advisors, we learned more about the purpose and basics of modeling in synthetic biology. After downloading the projects of previous year teams of the KUleuven to understand the inner workings of their model.
