Team:Paris-Saclay/Project/Notebook/Week 4
From 2012.igem.org
(Difference between revisions)
YohannPetiot (Talk | contribs) |
(→Week 4) |
||
(2 intermediate revisions not shown) | |||
Line 28: | Line 28: | ||
<a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract"> | <a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract"> | ||
<div class="child-tile"><p class="child-tile">GEMOTE Project</p></div> | <div class="child-tile"><p class="child-tile">GEMOTE Project</p></div> | ||
- | <img src=" | + | <img src="https://static.igem.org/mediawiki/2012/7/7c/Project-1.png" alt="" /> |
</a> | </a> | ||
</div> | </div> | ||
<div> | <div> | ||
<a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract"> | <a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract"> | ||
- | <img src=" | + | <img src="https://static.igem.org/mediawiki/2012/d/d1/Project2.jpg" alt="" /> |
<div class="child-tile"><p class="child-tile">GEMOTE Project</p></div> | <div class="child-tile"><p class="child-tile">GEMOTE Project</p></div> | ||
</a> | </a> | ||
Line 50: | Line 50: | ||
<div id="content-paris-saclay"> | <div id="content-paris-saclay"> | ||
='''Week 4'''= | ='''Week 4'''= | ||
- | + | ||
[[Category:Team:Paris-Saclay/Project Gemote/Notebook|d]] | [[Category:Team:Paris-Saclay/Project Gemote/Notebook|d]] | ||
__NOTOC__ | __NOTOC__ | ||
- | *We | + | *We placed an order for the primers. |
- | *DNA (biobricks) Resuspension using iGEM protocol | + | *DNA (biobricks) Resuspension using iGEM protocol. |
- | * | + | *Thermal shock treatment of each biobrick to have a large quantity of DNA. |
- | *Staggering of the transformed bacteria on a selective medium to select bacteria which | + | *Staggering of the transformed bacteria on a selective medium to select bacteria which recieved the plasmid. |
- | *We | + | *We started some colonies, one per biobrick, on a liquid culture, in order to make a Miniprep. |
- | *Miniprep to purify each biobrick (ready to use) | + | *Miniprep to purify each biobrick (ready to use). |
- | *Groove for two colonies because they did not | + | *Groove for two colonies because they did not grow on the liquid culture. |
- | + | ||
{{Team:Paris-Saclay/Follow}} | {{Team:Paris-Saclay/Follow}} |
Latest revision as of 00:29, 27 September 2012
Week 4
- We placed an order for the primers.
- DNA (biobricks) Resuspension using iGEM protocol.
- Thermal shock treatment of each biobrick to have a large quantity of DNA.
- Staggering of the transformed bacteria on a selective medium to select bacteria which recieved the plasmid.
- We started some colonies, one per biobrick, on a liquid culture, in order to make a Miniprep.
- Miniprep to purify each biobrick (ready to use).
- Groove for two colonies because they did not grow on the liquid culture.
Follow us !