EPF-Lausanne/7 July 2009
From 2009.igem.org
(Difference between revisions)
(→People in the lab) |
|||
(19 intermediate revisions not shown) | |||
Line 6: | Line 6: | ||
<body> | <body> | ||
<form action="input_button.htm"> | <form action="input_button.htm"> | ||
+ | <p align="right"> | ||
<input type="button" name="lien" value="6 July 2009" | <input type="button" name="lien" value="6 July 2009" | ||
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/6_July_2009'"> | onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/6_July_2009'"> | ||
- | + | <input type="button" name="lien" value="8 July 2009" | |
- | <input type="button" name="lien" value="8 July 2009 | + | |
onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/8_July_2009'"> | onClick="self.location.href='https://2009.igem.org/EPF-Lausanne/8_July_2009'"> | ||
</p> | </p> | ||
Line 53: | Line 53: | ||
==People in the lab== | ==People in the lab== | ||
:Tu, Heidi, Rafael, Basile, Nath | :Tu, Heidi, Rafael, Basile, Nath | ||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
+ | <html><center><a href="https://2009.igem.org/EPF-Lausanne/6_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/8_July_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 08:49, 28 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)
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