Team:Goettingen/week7-2

From 2012.igem.org

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<ul>
<ul>
<li>Experiment: <br>  
<li>Experiment: <br>  
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In order to gain further plasmid material over night cultures of all eight <i>flhDC</i>-promoter constructs were prepared for subsequent plasmid isolation. <br>
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In order to gain further plasmid material over night cultures of one colonie of all eight <i>flhDC</i>-promoter constructs were prepared for subsequent plasmid isolation. <br>
20E - #2 <br>
20E - #2 <br>
20G - #1 <br>
20G - #1 <br>
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<h2><b>V06_13 </b></h2><br>
<h2><b>V06_13 </b></h2><br>
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<b>V06_08_1 Miniprep of the new <i>flhDC</i>-promoter constructs</b><br>
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<b>V06_13_1 Miniprep of the new <i>flhDC</i>-promoter constructs</b><br>
<ul>
<ul>
<li>Experiment:  <br>
<li>Experiment:  <br>
Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual.  
Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual.  
<li>
<li>
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<br>
<br>
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<b>V06_08_2 Chemical transformartion of all <i>flhDC</i>-promoter constructs into E. coli (DH10B)</b><br>
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<b>V06_013_2 Chemical transformartion of pBAD-glGFP into E. coli (DH10B)</b><br>
<ul>
<ul>
<li>Experiment:  <br>
<li>Experiment:  <br>
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<li>Observations & Results: <br>
<li>Observations & Results: <br>
The transformation was successful since all plates showed numeours colonoes except the negative control.</li>
The transformation was successful since all plates showed numeours colonoes except the negative control.</li>
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</table>
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<h2><b>V06_14 </b></h2><br>
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<b>Preparation of over night cultures</i></b><br>
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<ul>
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<li>Experiment: <br>
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Over night cultures of pBAD-glGFP were prepared in order to isolate the plasmids. <br>
<br></td></tr>
<br></td></tr>
</table>
</table>

Revision as of 10:32, 14 September 2012