EPF-Lausanne/7 July 2009

From 2009.igem.org

(Difference between revisions)
(People in the lab)
(People in the lab)
Line 62: Line 62:
<html>
<html>
<body>
<body>
-
<form action="bouton.htm">
 
-
<div>
 
-
<button name="cliquemoi" type="button"
 
-
  value="SELFHTML" onClick="self.location.href='http://actuel.fr.selfhtml.org/'">
 
-
<p><img src="selfhtml.gif" width="106" height="109" border="0" alt="SELFHTML"><br>
 
-
<b>page d'accueil de SELFHTML</b></p>
 
-
</button>
 
-
</div>
 
-
</form>
 
-
</body>
 
-
</html>
 
-
 
-
<br>
 
-
 
-
<html>
 
-
<head>
 
-
<title>Texte du titre</title>
 
-
</head>
 
-
<body>
 
-
<h1>Liens sous une autre forme</h1>
 
<form action="bouton.htm">
<form action="bouton.htm">
<div>
<div>

Revision as of 07:58, 28 July 2009

Contents

7 July 2009




Wet Lab

We have to grow the 3 strains generously sent by Tom Beatty

The three strains are :

  • R.Palustris CEA001 (wild type) ; should be grown on LB medium only
  • R.Palustris BPHP1+ ; should be grown on LB with gentamycin (100 micrograms/ml)
  • E.Coli DH10B (pBPH/hmu0) ; should be grown on LB with gentamycin (20 micorgrams/ml)


The transformed LOVTAP and TrpR worked well (N.B. the plasmid of TrpR is pUC19 so the antibiotic resistance is Amp -> see below)


pUC19 plasmid


We did the glycerol stock, located in the -80 fridge, first floor of the iGEM compartement.

Then, a miniprep was done with both cultures. A LOVTAP plasmid aliquot was done, a TrpR plasmid aliquot was done, located in the -20 fridge, 2nd floor.


Cloning Strategy

To design plasmids : software Vector NTI


People in the lab

Tu, Heidi, Rafael, Basile, Nath