Team:Goettingen/week1-2

From 2012.igem.org

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Language: <img height="20", src="http://www.patrickreinke.de/igem/eng.jpg"> English, <img height="20", src="http://www.patrickreinke.de/igem/deu.jpg"> <a href="https://2012.igem.org/Team:Goettingen/main_deu">Deutsch</a> <br>
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<h2><b><a name="week3#2">#2 Speed Improvement - 1st week</a></b></h2>
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<h2><b><a name="week3#2">#3 Chemoreceptor Library - 1st 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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<h2><b><a name="week1#2#V05_03">V05_03</a></b></h2><br>
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<h2><b>V5_04 </b></h2><br>
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<b>Isolation of genomic DNA of <i>E. Coli</i> (strain DH10B)</b><br>
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<b>TITEL</b><br>
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<li>Experiment: <br> The genomic DNA of <i>E. coli</i> was isolated according to LINK!</li>
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<li>Experiment: <br>TEXTXTTXTuick Change overlapping PCR was performed using designed primers and Pfu Turbo polymerase (see Quick Change protocol in "protocols"). Was not succesful. We Could not observed any PCR product.</li>
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<li>Description: <br> </li>
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<li>Observations & Results: <br> </li>
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<h2><b>V5_04 </b></h2><br>
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<b>TITEL</b><br>
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<li>Experiment: <br>TEXTXTTXTuick Change overlapping PCR was performed using designed primers and Pfu Turbo polymerase (see Quick Change protocol in "protocols"). Was not succesful. We Could not observed any PCR product.</li>
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<h2><b>V09_4_1 </b></h2><br>
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<b>Test digestion of Psb1c3(including FlHDC under the control of different promoters) with</b><br>
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<li>Experiment: <br>Test digestion of Psb1c3 including FlHDC under the expression of 8 different promoters with the restriction enzymes EcoRI and PstI. Test digest worked for all clones.</li>
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<h2><b>V09_4_2 </b></h2><br>
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<b>Biobrick Standardization of motA, motB and yhjH</b><br>
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<li>Experiment: <br> PCR of motA, motB and yhjH using primers containing the standard BioBrick sequences. Procedure was succesful and the PCR products were purified via PeqGOLD Gelextraction Kit (Peqlab).</li>
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<h2><b>V09_5_1 </b></h2><br>
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<b>Double Digest of motA, motB, yhjH and Psb1c3</b><br>
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<li>Experiment: <br> MotA, motB, yhjH and Psb1c3 were digested with EcoRI and PsT1. The prodcuts were seperated via gel electrophoresis and purified using PeqGOLD Gelextraction Kit (Peqlab).</li>
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<h2><b>V09_5_2 </b></h2><br>
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<b>Quickchange of FliC</b><br>
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<li>Experiment: <br> Quick Change overlapping PCR was performed using designed primers and Pfu Turbo polymerase (see Quick Change protocol in "protocols"). Was not succesful. We Could not observed any PCR product.</li>
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<h2><b>V09_6 </b></h2><br>
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<b>Ligation and Transformation of motA, motB and yhjH</b><br>
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<li>Experiment: <br> After the ligation of motA, motB and yhjH into the plasmid Psb1c3, the ligation products were transformed into the E. coli strain DH10B.</li>
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<a href="#top">&uarr; Return to top</a>
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<a href="https://2012.igem.org/Team:Goettingen/Notebook">Back to overview</a><br>
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<b>Important pages</b>:<br>
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<a href="https://2012.igem.org/Team:Goettingen">Home</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Team">Team</a>;
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<a href="https://igem.org/Team.cgi?year=2012">Official Team Profile</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Project">Project</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Parts">Parts submitted to the Registry</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Modeling">Modeling</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Notebook">Notebook</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Saftey">Saftey</a>;
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<a href="https://2012.igem.org/Team:Goettingen/Attributions">Attributions</a>
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Revision as of 13:10, 11 September 2012

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