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| - | <br><h2>Get to know our virus</h2>
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| - | <!---Insert Text in here---> Our project starts with first sequence analysis.
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/March" ><img src="https://static.igem.org/mediawiki/2010/2/21/Freiburg10_Labjournal-March.png" /></a></div></div>
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| - | <br><h2>Checking iGEM compatibility </h2>
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| - | <!---Insert Text in here--->Scanning for iGEM restriction sites:<br/>
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| - | • Vector plasmid <br/>
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| - | • Thymidine kinase<br/>
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| - | • Cytosindeaminase<br/>
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/April" ><img src="https://static.igem.org/mediawiki/2010/6/6b/Freiburg10_Labjournal-April.png" /></a></div></div>
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| - | <br><h2>First practical steps</h2>
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| - | <!---Insert Text in here--->We took a closer look to the theoretical DNA- and amino acid sequence of the ITRs, questioned the role of the β-globin intron, had a closer look to the CMV promoter and performed our first cloning attempt.
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/May" ><img src="https://static.igem.org/mediawiki/2010/6/61/Freiburg10_Labjournal-May.png" /></a></div></div>
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| - | <br><h2>First fluorescing HT1080 cells</h2>
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| - | <!---Insert Text in here--->We conducted our first site-directed mutagenesis. <br/>
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| - | First cell culture steps:<br/>
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| - | • Splitting and seeding of AAV 293 and HT1080 cells<br/>
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| - | • Calcium phosphate transfection<br/>
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| - | • Transduction with virus particles containing YFP encoding sequence<br/>
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| - | • Microscopy: Fluorescent transduced HT1080 cells<br/>
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| - | We planned to determine infectious virus titer via quantitative real-time PCR. For this purpose primers were designed, transduced HT1080 cells were harvested and prepared.<br/>
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| - | Theoretical studies of the AAV structure: Impressions.
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/June" ><img src="https://static.igem.org/mediawiki/2010/4/48/Freiburg10_Labjournal-June.png" /></a></div></div>
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| - | <br><h2>Modifying Rep/Cap & Modularizing Vector plasmid</h2>
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| - | <!---Insert Text in here--->We developed a plan for modifying the surface exposed loops of the virus capsid.
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| - | For this purpose not only 5 iGEM restriction sites, but also the so called ViralBrick restriction sites located in the Rep/Cap sequence needed to be deleted: BamHI, SalI <br/>
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| - | BioBrick production of the inverted terminal repeats (ITRs) turned out to be difficult. Therefore the alternative “ITR fancy method” was developed. We successfully produced AAV2 left and right ITR fused to the RFC10 prefix.<br/>
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| - | Further on we received first quantitative transduction results via flow cytometry.<br/>
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| - | mGMK_TK30 was successfully cloned into the vector plasmid.
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/July" ><img src="https://static.igem.org/mediawiki/2010/d/dc/Freiburg10_Labjournal-July.png" /></a></div></div>
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| - | <br><h2>Producing more BioBricks</h2>
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/August" ><img src="https://static.igem.org/mediawiki/2010/0/06/Freiburg10_Labjournal-AugustI.png" /></a></div></div>
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/August2" ><img src="https://static.igem.org/mediawiki/2010/b/b1/Freiburg10_Labjournal-AugustII.png" /></a></div></div>
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| - | <div class="lab_journal_img"><a href="https://2010.igem.org/Team:Freiburg_Bioware/NoteBook/Labjournal/September" ><img src="https://static.igem.org/mediawiki/2010/1/1e/Freiburg10_Labjournal-SeptemberI.png" /></a></div></div>
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