Difference between revisions of "Team:EPF Lausanne/Notebook/Yeast"
| Line 75: | Line 75: | ||
<div id="integrate_pTPGI_dCas9_VP64" class="panel"> | <div id="integrate_pTPGI_dCas9_VP64" class="panel"> | ||
<h1><small>Integrate pTPGI_dCas9_VP64</small></br>Integrate pTPGI_dCas9_VP64</h1> | <h1><small>Integrate pTPGI_dCas9_VP64</small></br>Integrate pTPGI_dCas9_VP64</h1> | ||
| − | <p><small>We received plasmid pTPGI_dCas9_VP64 in bacteria from Addgene. The plasmid was found from the article "Tunable and multifunctional eukaryotic transcription factors based on Crispr/Cas". After glycerol stocks and miniprep, we performed a restriction analysis to check the identity of our plasmid. We linearised the plasmid, in order to integrate it into yeast genome. For more details about our experiments, see <a target="_blank" href="">here</a>. | + | <p><small>We received plasmid pTPGI_dCas9_VP64 in bacteria from Addgene. The plasmid was found from the article "Tunable and multifunctional eukaryotic transcription factors based on Crispr/Cas". After glycerol stocks and miniprep, we performed a restriction analysis to check the identity of our plasmid. We linearised the plasmid, in order to integrate it into yeast genome. For more details about our experiments, see <a target="_blank" href="https://static.igem.org/mediawiki/2015/3/30/EPF_Lausanne_Journal_integrate_dCas9-VP64.pdf">here</a>. |
</small></p> | </small></p> | ||
Revision as of 09:28, 19 August 2015
saccharomyces cerevisiae
Integrate pTPGI_dCas9_VP64Integrate pTPGI_dCas9_VP64
We received plasmid pTPGI_dCas9_VP64 in bacteria from Addgene. The plasmid was found from the article "Tunable and multifunctional eukaryotic transcription factors based on Crispr/Cas". After glycerol stocks and miniprep, we performed a restriction analysis to check the identity of our plasmid. We linearised the plasmid, in order to integrate it into yeast genome. For more details about our experiments, see here.
Materials and method
- Glycerol stocks
- Miniprep
- Restriction analysis
- Polymerase Chain Reaction
- Yeast integration
Results
We used four different sets of enzymes for the restriction analysis. Linearized pTPGI_dCas9_VP64 is expected to be 10'987 bp. We observe that the gel (fig.1) corresponds to the expected one. The plasmid was linearised both with EagI HF and NotI HF prior to integration. We integrated each linearised plasmid to obtain two different yeast strains.
Integrate reporter plasmidLinearise reporter plasmid
We received plasmid pCYC_yeGFP in bacteria from Addgene. The plasmid was found from ... We inoculated single colonies of bacteria in order to prepare glycerol stocks and minipreps. We performed a restriction analysis to check the identity of our plasmid. We linearised the plasmid by PCR, in order to integrate it into yeast genome.
Materials and method
- Glycerol stocks
- Miniprep
- Restriction analysis
- Polymerase Chain Reaction
Results
We used four different sets of enzymes for the restriction analysis. Linearized pCYC_yeGFP is expected to be 10'987 bp. We observe that the gel (fig.1) corresponds to the expected one (fig. 2). The plasmid was linearised both with ... and ... prior to integration. We integrated each linearised plasmid to obtain two different yeast strains.
Integrate reporter plasmidSynthesize promoters
The promoter CYC#0 was already present in plasmid pCYC_yeGFP from Addgene. We synthesized three other promoters CYC#1, CYC#2 and CYC#3. The only differences between one another were the three gRNA SDSs c3, c6 and c7.
Materials and method
- Synthesis ??
Results
We obtain four different promoters CYC#0, CYC#1, CYC#2 and CYC#3 according to fig. ...
