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Team:Macquarie Australia/Notebook
From 2013.igem.org
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<center><h1>Notebook</h1></center> | <center><h1>Notebook</h1></center> | ||
| - | <center><h7> <p> To browse through our notebook simply click on the image with the date. It will expand with what we did that week. To continue on simply click on the next one. If the notebook isn't functioning as planned (it will not load the next tab of content) then please go to our linearised view which is located <a href="https://2013.igem.org/Team:Macquarie_Australia/Notebook2">here</a>.</p></h7></center><br><br> | + | <center><h7> <p> To browse through our notebook simply click on the image with the date. It will expand with what we did that week. To continue on simply click on the next one. If the notebook isn't functioning as planned (it will not load the next tab of content) then please go to our linearised view which is located <a href="https://2013.igem.org/Team:Macquarie_Australia/Notebook2">here</a>.</p></h7><br> A seperate |
| + | <td></td><td><span style="color:#8B0000"><font size = 3><a class="three" href='https://2013.igem.org/Team:Macquarie_Australia/Results'><b>'Results & Characterization'</b></a></font size></span> section has been created to show and highlight our successful accomplishments, shown A seperate ' | ||
| + | <td></td><td><span style="color:#8B0000"><font size = 3><a class="three" href='https://2013.igem.org/Team:Macquarie_Australia/Results'><b>Here</b></a></font size></span> section has been created to show and highlight our successful accomplishments. . | ||
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Intro to the week, Work being done, "Using PCR we amplified the genes X and X"<br> | Intro to the week, Work being done, "Using PCR we amplified the genes X and X"<br> | ||
Revision as of 12:30, 5 September 2013
Notebook
To browse through our notebook simply click on the image with the date. It will expand with what we did that week. To continue on simply click on the next one. If the notebook isn't functioning as planned (it will not load the next tab of content) then please go to our linearised view which is located here.
A seperate
Intro to the week, Work being done, "Using PCR we amplified the genes X and X"
Results (This worked, this didnt), "Gene X didnt amplify, Gene X did"
Small discussion + Whats next "We plan on then doing X to amplified gene"
With the break between semesters over, the Macquarie iGEM team returned to classes; for many of us this was the first day of iGEM 2013. We had our first meeting and discussed our project. Dr. Louise Brown and Associate Professor Rob Willows were introduced to the team and we began to determine who would take on certain roles within the team.
We eagerly began our project, deciding to use Gibson Assembly to produce our optimised genes. We had decided to develop BioBricks necessary for the biosynthesis of chlorophyll within E.coli. To do this, we constructed a gene pathway, containing 12 genes to reach our goal of chlorophyll biosynthesis.
Week 2 (G block assemblies & transformations) - Update Coming soon
