Team:Amsterdam/project/diary/lab

From 2012.igem.org

(Difference between revisions)
(Undo revision 63227 by ErnstBank (talk))
 
Line 3: Line 3:
{{Team:Amsterdam/Header}}
{{Team:Amsterdam/Header}}
{{Team:Amsterdam/Sidebar1}}
{{Team:Amsterdam/Sidebar1}}
 +
<html>
<div id="main-content">
<div id="main-content">
-
<p></p>
+
<p>
 +
<b><center><h1>Lab Journal</h1></center></b>
 +
</p>
 +
 
 +
<p>
 +
<b><center><h2>April</h2></center></b>
 +
</p>
 +
 
 +
<p>
 +
<u><center><h4>26/04/2012</h4></center></u>
 +
</p>
 +
 
 +
<p>
 +
We arrive at the lab to get started! First items on the agenda are getting settled at the lab and acquiring our needed equipment. As a bonus we do a transformation need tot test the Gibson method we will be using throughout these months.
 +
We will do this by cloning a GFP into a pET28 vector using our transformation protocol.
 +
</p>
 +
 
 +
<p>
 +
<u><center><h4>27/04/2012</h4></center></u>
 +
</p>
 +
 
 +
<p>
 +
Succesfully transformed the plasmids. Ordered the primers for our gibson assembly and started to prepare things. Aliquoting our phusion and gisbon master mix.
 +
</p>
 +
 
 +
<p>
 +
<b><center><h2>May</h2></center></b>
 +
</p>
 +
 
 +
<p>
 +
<u><center><h4>07/05/2012</h4></center></u>
 +
</p>
 +
 
 +
<p>
 +
Preparing O/N cultures which can be taken out of 37C in the weekend by a friend
 +
</p>
 +
 
 +
<p>
 +
<u><center><h4>08/05/2012</h4></center></u>
 +
</p>
 +
 
 +
<p>
 +
Our friend former igem member Yuri of 2011 will take out our O/N cultures.
 +
</p>
 +
 
 +
<p>
 +
<u><center><h4>09/05/2012</h4></center></u>
 +
</p>
 +
 
 +
<p>
 +
Yuri forgot... Start again. Note; rely on ourselves
 +
</p>
 +
 
 +
<p>
 +
<u><center><h4>10/05/2012</h4></center></u>
 +
</p>
 +
 
 +
<p>
 +
The primers arrived. we reconstituded them and tried them on the plasmids after mini-prepping our O/N culture.
 +
Gel:
 +
Starting our first PCR.
 +
</p>
 +
 
 +
 
 +
 
 +
 
 +
 
</div>
</div>
 +
</html>
{{Team:Amsterdam/Foot}}
{{Team:Amsterdam/Foot}}

Latest revision as of 12:08, 9 August 2012

Lab Journal

April

26/04/2012

We arrive at the lab to get started! First items on the agenda are getting settled at the lab and acquiring our needed equipment. As a bonus we do a transformation need tot test the Gibson method we will be using throughout these months. We will do this by cloning a GFP into a pET28 vector using our transformation protocol.

27/04/2012

Succesfully transformed the plasmids. Ordered the primers for our gibson assembly and started to prepare things. Aliquoting our phusion and gisbon master mix.

May

07/05/2012

Preparing O/N cultures which can be taken out of 37C in the weekend by a friend

08/05/2012

Our friend former igem member Yuri of 2011 will take out our O/N cultures.

09/05/2012

Yuri forgot... Start again. Note; rely on ourselves

10/05/2012

The primers arrived. we reconstituded them and tried them on the plasmids after mini-prepping our O/N culture. Gel: Starting our first PCR.