EPF-Lausanne/24 September 2009

From 2009.igem.org

(Difference between revisions)
(Wet Lab)
 
Line 7: Line 7:
<form action="input_button.htm">
<form action="input_button.htm">
<p align="right">
<p align="right">
-
<input type="button" name="lien" value="23 September 2009"
+
<input type="button" name="lien" value="22 September 2009"
-
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/23_September_2009'">
+
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/22_September_2009'">
<input type="button" name="lien" value="25 September 2009"  
<input type="button" name="lien" value="25 September 2009"  
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/25_September_2009'">
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/25_September_2009'">
Line 47: Line 47:
-
<html><center><a href="https://2009.igem.org/EPF-Lausanne/23_September_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/22_September_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/25_September_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/25_September_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 15:21, 4 October 2009

Contents

24 September 2009





Wet Lab

Transformation in Trp K.O.

The 3 newly competent strains (JW4356-2, JRG 1046, JRG 465) will be transformed with :

- RO2#4 + BB1 (+Amp, Kana) -> double transformation.

- RO2#4 (+Kana)

- RO1#1 (+Kana)

- RO1#1 + BB1 (+Amp, Kana) -> double transformation.

Note : the 3 control (1 ug/ul DNA, 100 pg/ul DNA, 10 pg/ul DNA -> 10ul for each transf) + KANA. We will count the nb of clones the next morning on the plates to determine transformation efficiency.

The normal protocol for these transformation has been used (50 ul cells + 10 ul total volume DNA) : 20 min on ice, heat shoch (45 s at 42°C), SOB (500ul) at 37°C for 1 h, plated on according antibiotic LB/Agar plates. Put overnight at 37°C.

Note : the double transformation : the whole tue (about 560 ul) is added to the plates. The single transformation : only 150 ul of the mixture.

People in the lab

Mél, Nicolas, Christian, Basile