Difference between revisions of "Team:EPF Lausanne/Timeline"
| Line 16: | Line 16: | ||
<div class="timeline-section"> | <div class="timeline-section"> | ||
<ul class="timeline"> | <ul class="timeline"> | ||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
<li class="timeline-inverted"> | <li class="timeline-inverted"> | ||
<div class="timeline-badge"></div> | <div class="timeline-badge"></div> | ||
| Line 35: | Line 25: | ||
<div class="timeline-body"> | <div class="timeline-body"> | ||
<p>The E. Coli part of our project is strongly based on the paper of Bikard et al. "Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system". Bikard sent us his strains JEN202, JEN202+PWJ89 and DH5A+PWJ66. We also ordered a plasmid containing dCas9 and the synthetic DNA encoding fou our gRNAs.</p> | <p>The E. Coli part of our project is strongly based on the paper of Bikard et al. "Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system". Bikard sent us his strains JEN202, JEN202+PWJ89 and DH5A+PWJ66. We also ordered a plasmid containing dCas9 and the synthetic DNA encoding fou our gRNAs.</p> | ||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
</div> | </div> | ||
</div> | </div> | ||
| Line 57: | Line 37: | ||
<div class="timeline-body"> | <div class="timeline-body"> | ||
<p>In our project dCas9 target DNA sequences using gRNAs and acts as an activator or an inhibitor depending on its position. Axel and Cyril created a C++ program to blast random generated gRNA sequences on the E. Coli or Yeast genome.</p> | <p>In our project dCas9 target DNA sequences using gRNAs and acts as an activator or an inhibitor depending on its position. Axel and Cyril created a C++ program to blast random generated gRNA sequences on the E. Coli or Yeast genome.</p> | ||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
</div> | </div> | ||
</div> | </div> | ||
| Line 130: | Line 98: | ||
<div class="timeline-body"> | <div class="timeline-body"> | ||
<p>First meeting with everyone: 12 teammates, 7 TAs and 3 advisors.</p> | <p>First meeting with everyone: 12 teammates, 7 TAs and 3 advisors.</p> | ||
| − | <img src="https://static.igem.org/mediawiki/2015/2/2e/Team_All.jpg" width=" | + | <img src="https://static.igem.org/mediawiki/2015/2/2e/Team_All.jpg" width="100%" lass="displayed"> |
</div> | </div> | ||
</div> | </div> | ||
Revision as of 08:40, 12 August 2015
Timeline
-
The bible
The E. Coli part of our project is strongly based on the paper of Bikard et al. "Programmable repression and activation of bacterial gene expression using an engineered CRISPR-Cas system". Bikard sent us his strains JEN202, JEN202+PWJ89 and DH5A+PWJ66. We also ordered a plasmid containing dCas9 and the synthetic DNA encoding fou our gRNAs.
-
Blast
02.04.2015
In our project dCas9 target DNA sequences using gRNAs and acts as an activator or an inhibitor depending on its position. Axel and Cyril created a C++ program to blast random generated gRNA sequences on the E. Coli or Yeast genome.
-
And the winner is...
26.03.2015
...the new framework for biologic circuits using dCas9.
-
The lab starts!
24.03.2015 - 26.03.2015
TAs start to train us in the lab: medium and agar plates preparation
-
Brainstorming finalists
19.03.2015
Three cool ideas came out of the brainstorming: a new framework for biologic circuits or lung cancer therapy using dCas9 and cell-cell communication through exosomes.
-
Brainstorming
26.02.2015 - 12.03.2015
The team is split into small groups, brainstorming for an interesting project that will occupy us during the summer.
-
First meeting: iGEM officially starts!
19.02.2015
First meeting with everyone: 12 teammates, 7 TAs and 3 advisors.
