Team:Goettingen/week10-2

From 2012.igem.org

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<h2><b><a name="week8#2">#2 Speed Improvement - 10th week</a></b></h2>
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<h2><b><a name="week10#2">#2 Speed Improvement - 10th week</a></b></h2>
<a href="https://2012.igem.org/Team:Goettingen/Notebook">Back to overview</a><br>
<a href="https://2012.igem.org/Team:Goettingen/Notebook">Back to overview</a><br>
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<br>
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<h2><b>Versuchsnummer </b></h2><br>
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<b>TITEL</i></b><br>
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<h2><b>V06_11 </b></h2><br>
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<ul>
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<b>V06_11_1 Miniprep of the new <i>flhDC</i>-promoter constructs</b><br>
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<li>Experiment: <br>  
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TEXT.<br>
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        <ul>
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                <li>Experiment: <br>
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Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual.
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        </ul>
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</li>
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<b>V06_11_2 Chemical retransformartion of the new <i>flhDC</i>-promoter constructs into <i>E. coli</i> (DH10B)</b><br>
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        <ul>
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                <li>Experiment:  <br>
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For the chemical retransformation the standard protocol for transformation was followed. The following constructs were transformed into <i>E. coli</i>:<br>
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20G - #1 <br>
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20G - #2 <br>
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2G - #1 <br>
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2G - #2 <br>
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2G - #3 <br>
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20I - #2 <br>
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20I - #3 <br>
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18O - #2 <br>
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18O - #3 <br>
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18K - #1 <br>
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18K - #2 <br>
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18K - #3 <br></li>
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                <li>Observations & Results: <br>
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The retransformation was successful since all plates showed numeours colonoes except the negative control.
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    </ul>
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<h2><b>V06_12 </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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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>
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20E - #2 <br>
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20G - #1 <br>
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2G - #1 <br>
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20I - #2 <br>
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18M - #2 <br>
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18O - #2 <br>
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18K - #1 <br>
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18C - #2 <br>
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</table>
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<h2><b>Versuchsnummer </b></h2><br>
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<br>
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<b>TITEL</b><br>
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<h2><b>V06_13 </b></h2><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>
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Text</li>
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Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual.</li></ul>
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</li></ul>
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<br>
<br>
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<b>V06_13_2 Chemical transformartion of pBAD-<i>sfGFP</i> into <i>E. coli</i> (DH10B)</b><br>
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<ul>
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<li>Experiment:  <br>
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For the chemical transformation the standard protocol was followed. <br>
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<li>Observations & Results: <br>
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The transformation was successful since all plates showed numeours colonoes except the negative control.</li>
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</ul><br>
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<h2><b>Versuchsnummer </b></h2><br>
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<h2><b>V06_14 </b></h2><br>
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<b> Titel</i></i></b><br>
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<b> Preparation of over night cultures</i></i></b><br>
<ul>
<ul>
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<li>Experiment: <br>  
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<li>Experiment: <br>
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Text<br>
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Over night cultures of the pBAD-<i>sfGFP</i> clones were prepared in order to isolate the plasmids. <br>
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<br></td></tr>
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</table>
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<br>
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<table cellpadding="20 px" border="1" bordercolor="black" valign="top">
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<h2><b>V06_15 </b></h2><br>
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<b> Miniprep of pBAD-<i>sfGFP</i></i></i></b><br>
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<ul>
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<li>Experiment: <br>
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Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual. <br>
<br></td></tr>
<br></td></tr>
</table>
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Revision as of 14:19, 16 September 2012