EPF-Lausanne/1 August 2009

From 2009.igem.org

(Difference between revisions)
 
(3 intermediate revisions not shown)
Line 9: Line 9:
<input type="button" name="lien" value="31 July 2009"
<input type="button" name="lien" value="31 July 2009"
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/31_July_2009'">
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/31_July_2009'">
-
<input type="button" name="lien" value="02 August 2009"  
+
<input type="button" name="lien" value="03 August 2009"  
-
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/2_August_2009'">
+
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/3_August_2009'">
</p>
</p>
</form>
</form>
Line 28: Line 28:
We checked the plates from the transformation of the previous day: only 7 clones grew on the LacI-RBS (not gel extracted) plate. We did a colony PCR with each of the clones that grew to check which clones potentially contained the desired fragment. To check this, we then ran agarose gel with samples of each of the PCRs. The result: 3 of the clones gave a fragment of the expected length!!!
We checked the plates from the transformation of the previous day: only 7 clones grew on the LacI-RBS (not gel extracted) plate. We did a colony PCR with each of the clones that grew to check which clones potentially contained the desired fragment. To check this, we then ran agarose gel with samples of each of the PCRs. The result: 3 of the clones gave a fragment of the expected length!!!
 +
What was left of these clones was then put into liquid culture and left to incubate at 37°C.
What was left of these clones was then put into liquid culture and left to incubate at 37°C.
 +
 +
At around 30 past midnight minipreps of these clones were done!
==People in the lab==
==People in the lab==
Line 35: Line 38:
-
<html><center><a href="https://2009.igem.org/EPF-Lausanne/30_July_2009"><img src="https://static.igem.org/mediawiki/2009/thumb/6/61/Flèche_gauche.png/70px-Flèche_gauche.png"></a>   
+
<html><center><a href="https://2009.igem.org/EPF-Lausanne/31_July_2009"><img src="https://static.igem.org/mediawiki/2009/thumb/6/61/Flèche_gauche.png/70px-Flèche_gauche.png"></a>   
-
<a href="https://2009.igem.org/EPF-Lausanne/1_August_2009"><img src="https://static.igem.org/mediawiki/2009/thumb/5/5e/Fleche_droite.png/70px-Fleche_droite.png"></a></center></html>  
+
<a href="https://2009.igem.org/EPF-Lausanne/3_August_2009"><img src="https://static.igem.org/mediawiki/2009/thumb/5/5e/Fleche_droite.png/70px-Fleche_droite.png"></a></center></html>  
</div><div CLASS="epfl09bouchon"></div>
</div><div CLASS="epfl09bouchon"></div>

Latest revision as of 19:56, 2 August 2009

Contents

1 August 2009





Wet Lab

We checked the plates from the transformation of the previous day: only 7 clones grew on the LacI-RBS (not gel extracted) plate. We did a colony PCR with each of the clones that grew to check which clones potentially contained the desired fragment. To check this, we then ran agarose gel with samples of each of the PCRs. The result: 3 of the clones gave a fragment of the expected length!!!

What was left of these clones was then put into liquid culture and left to incubate at 37°C.

At around 30 past midnight minipreps of these clones were done!

People in the lab

Nath, Basile, Gab