"
Team:Freiburg Bioware/NoteBook/Labjournal
From 2010.igem.org
(Difference between revisions)
| Line 60: | Line 60: | ||
<p class="boxes_labjournal_day">Labday 2- 5</p> | <p class="boxes_labjournal_day">Labday 2- 5</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...ordering AAV-2 Helper-free System...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 69: | Line 69: | ||
<p class="boxes_labjournal_day">Labday 6- 17</p> | <p class="boxes_labjournal_day">Labday 6- 17</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...theoretical cloning...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 78: | Line 78: | ||
<p class="boxes_labjournal_day">Labday 18- 45</p> | <p class="boxes_labjournal_day">Labday 18- 45</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...first transduced cells...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 87: | Line 87: | ||
<p class="boxes_labjournal_day">Labday 46- 75</p> | <p class="boxes_labjournal_day">Labday 46- 75</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...organizing the lab...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 96: | Line 96: | ||
<p class="boxes_labjournal_day">Labday 76- 92</p> | <p class="boxes_labjournal_day">Labday 76- 92</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...cloning parts...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 105: | Line 105: | ||
<p class="boxes_labjournal_day">Labday 93- 106</p> | <p class="boxes_labjournal_day">Labday 93- 106</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...assembled vector plasmid is working...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 114: | Line 114: | ||
<p class="boxes_labjournal_day">Labday 107- 123</p> | <p class="boxes_labjournal_day">Labday 107- 123</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...simply producing BioBricks...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 123: | Line 123: | ||
<p class="boxes_labjournal_day">Labday 124- 135</p> | <p class="boxes_labjournal_day">Labday 124- 135</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...21x mutated RepCap is working...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 132: | Line 132: | ||
<p class="boxes_labjournal_day">Labday 136- 149</p> | <p class="boxes_labjournal_day">Labday 136- 149</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...testing BioBricks by virus production...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 141: | Line 141: | ||
<p class="boxes_labjournal_day">Labday 150- 166</p> | <p class="boxes_labjournal_day">Labday 150- 166</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...Capsid modification works...</p> |
</a> | </a> | ||
</div> | </div> | ||
| Line 150: | Line 150: | ||
<p class="boxes_labjournal_day">Labday 166- 170</p> | <p class="boxes_labjournal_day">Labday 166- 170</p> | ||
<img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | <img src="https://static.igem.org/mediawiki/2010/3/35/Freiburg_10_BioBrick_icon.png" class="image_labjournal" /> | ||
| - | <p class="boxes_labjournal_text">... | + | <p class="boxes_labjournal_text">...Jemboree!!!...</p> |
</a> | </a> | ||
</div> | </div> | ||
Revision as of 17:04, 27 October 2010
Get to know our virus
Our project starts with first sequence analysis.
Checking iGEM compatibility
Scanning for iGEM restriction sites:• Vector plasmid
• Thymidine kinase
• Cytosindeaminase
First practical steps
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.
First fluorescing HT1080 cells
We conducted our first site-directed mutagenesis.First cell culture steps:
• Splitting and seeding of AAV 293 and HT1080 cells
• Calcium phosphate transfection
• Transduction with virus particles containing YFP encoding sequence
• Microscopy: Fluorescent transduced HT1080 cells
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.
Theoretical studies of the AAV structure: Impressions.
Modifying Rep/Cap & Modularizing Vector plasmid
We developed a plan for modifying the surface exposed loops of the virus capsid. 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, SalIBioBrick 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.
Further on we received first quantitative transduction results via flow cytometry.
mGMK_TK30 was successfully cloned into the vector plasmid.
Producing more BioBricks
Headline
Headline
Headline
Headline
Headline
Headline
https://2010.igem.org/Team:Freiburg_Bioware/NoteBook => Back to Notebook overview]
- March (labday 1)
- April (labday 2 - 5)
- May (labday 6 - 17)
- June (labday 18 - 45)
- July (labday 46 - 75)
- August part 1 (labday 76 - 92)
- August part 2 (labday 93 - 106)
- September part 1 (labday 107 - 123)
- September part 2 (labday 124 - 135)
- October part 1 (labday 136 - 149 )
- October part 2 (labday 150 - 166 )
- November (labday 167 - 170 )
- Cellculture
