Team:Goettingen/week7-2

From 2012.igem.org

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<h2><b>V06_11 </b></h2><br>
<h2><b>V06_11 </b></h2><br>
<b>V06_11_1 Miniprep of the new <i>flhDC</i>-promoter constructs</b><br>
<b>V06_11_1 Miniprep of the new <i>flhDC</i>-promoter constructs</b><br>
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<ul>
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        <ul>
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<li>Experiment: <br>
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                <li>Experiment: <br>
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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.
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</ul>
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        </ul>
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<br>
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<b>V06_11_2 Chemical retransformation 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 <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a> was followed. The following constructs were transformed into <i>E. coli</i>:<br>
<br>
<br>
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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 <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a> for transformation was followed. The following constructs were transformed into <i>E. coli</i>:<br>
 
20G - #1 <br>
20G - #1 <br>
20G - #2 <br>
20G - #2 <br>
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18K - #2 <br>
18K - #2 <br>
18K - #3 <br></li>
18K - #3 <br></li>
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                <li>Observations & Results: <br>
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<br>
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<li>Observations & Results: <br>
The retransformation was successful since all plates showed numeours colonies except the negative control.
The retransformation was successful since all plates showed numeours colonies except the negative control.
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</ul>
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<li>Experiment: <br>
<li>Experiment: <br>
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>
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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<br>
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20G - #1 <br>
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- 20E - #2 <br>
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2G - #1 <br>
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- 20G - #1 <br>
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20I - #2 <br>
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- 2G - #1 <br>
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18M - #2 <br>
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- 20I - #2 <br>
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18O - #2 <br>
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- 18M - #2 <br>
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18K - #1 <br>
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- 18O - #2 <br>
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18C - #2 <br>
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- 18K - #1 <br>
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- 18C - #2 <br>
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<br>
<br></td></tr>
<br></td></tr>
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Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual.</li></ul>
Minipreps were conducted with PeqGOLD MiniPrep Kit (Peqlab) according to the user manual.</li></ul>
<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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<b>V06_13_2 Chemical transformation of pBAD-<i>sfGFP</i> into <i>E. coli</i> (DH10B)</b><br>
<ul>
<ul>
<li>Experiment:  <br>
<li>Experiment:  <br>

Revision as of 09:38, 21 September 2012