Team:Goettingen/week15-3

From 2012.igem.org

(Difference between revisions)
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<td width="900" bordercolor="black" valign="top">
<h2><b>V08_06 </b></h2><br>
<h2><b>V08_06 </b></h2><br>
-
<b>V08_06_1 2<sup>st</sup> round: Ethanol precipitation of mutated plasmids</b><br>
+
<b>V08_06_1 2<sup>nd</sup> round: Ethanol precipitation of mutated plasmids</b><br>
<ul>
<ul>
<li>Experiment: <br>The ethanol precipitation was performed according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>.</li>
<li>Experiment: <br>The ethanol precipitation was performed according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>.</li>
</ul>
</ul>
<br>
<br>
-
<b>V08_06_2 2<sup>st</sup> round: Transformation of electrocompetent cells with the mutant plasmid mixture</b><br>
+
<b>V08_06_2 2<sup>nd</sup> round: Transformation of electrocompetent cells with the mutant plasmid mixture</b><br>
<ul>
<ul>
<li>Experiment: <br>Electrocompetent cells were prepared according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. The transformation was performed according to the established <a href="https://2012.igem.org/Team:Goettingen/week10-3">protocol</a>.</li>
<li>Experiment: <br>Electrocompetent cells were prepared according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>. The transformation was performed according to the established <a href="https://2012.igem.org/Team:Goettingen/week10-3">protocol</a>.</li>
 +
</ul>
 +
<br></td></tr>
 +
</table>
 +
<br>
 +
<table cellpadding="20 px" border="1" bordercolor="black" valign="top">
 +
<tr bordercolor="black" valign="top">
 +
<td width="900" bordercolor="black" valign="top">
 +
<h2><b>V08_07 </b></h2><br>
 +
<b>V08_07_1 2<sup>nd</sup> round: Analysis of transforamtion V08_06</b><br>
 +
<ul>
 +
<li>Experiment: <br>Plates and liquid culture were investigated.</li>
 +
</ul>
 +
<ul>
 +
<li>Observations & Results: <br>Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.</li>
 +
</ul>
 +
<br>
 +
<b>V08_07_2 2<sup>nd</sup> round: Mutagenesis PCR was set up again, 1000 µL</b><br>
 +
<ul>
 +
<li>Experiment: <br>PCR according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>.</li>
 +
</ul>
 +
<br></td></tr>
 +
</table>
 +
<br>
 +
<table cellpadding="20 px" border="1" bordercolor="black" valign="top">
 +
<tr bordercolor="black" valign="top">
 +
<td width="900" bordercolor="black" valign="top">
 +
<h2><b>V08_08 </b></h2><br>
 +
<b>V08_08_1 2<sup>nd</sup> round: Analysis of transforamtion V08_06</b><br>
 +
<ul>
 +
<li>Experiment: <br>Plates and liquid culture were investigated.</li>
 +
</ul>
 +
<ul>
 +
<li>Observations & Results: <br>Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.</li>
 +
</ul>
 +
<br>
 +
<b>V08_08_2 2<sup>nd</sup> round: Mutagenesis PCR was set up again, 1000 µL</b><br>
 +
<ul>
 +
<li>Experiment: <br>PCR according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>.</li>
 +
</ul>
 +
<br></td></tr>
 +
</table>
 +
<br>
 +
<table cellpadding="20 px" border="1" bordercolor="black" valign="top">
 +
<tr bordercolor="black" valign="top">
 +
<td width="900" bordercolor="black" valign="top">
 +
<h2><b>V08_09 </b></h2><br>
 +
<b>V08_09_1 2<sup>nd</sup> round: Analysis of transforamtion V08_06</b><br>
 +
<ul>
 +
<li>Experiment: <br>Plates and liquid culture were investigated.</li>
 +
</ul>
 +
<ul>
 +
<li>Observations & Results: <br>Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.</li>
 +
</ul>
 +
<br>
 +
<b>V08_09_2 2<sup>nd</sup> round: Mutagenesis PCR was set up again, 1000 µL</b><br>
 +
<ul>
 +
<li>Experiment: <br>PCR according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>.</li>
 +
</ul>
 +
<br></td></tr>
 +
</table>
 +
<br>
 +
<table cellpadding="20 px" border="1" bordercolor="black" valign="top">
 +
<tr bordercolor="black" valign="top">
 +
<td width="900" bordercolor="black" valign="top">
 +
<h2><b>V08_10 </b></h2><br>
 +
<b>V08_10_1 2<sup>nd</sup> round: Analysis of transforamtion V08_06</b><br>
 +
<ul>
 +
<li>Experiment: <br>Plates and liquid culture were investigated.</li>
 +
</ul>
 +
<ul>
 +
<li>Observations & Results: <br>Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.</li>
 +
</ul>
 +
<br>
 +
<b>V08_10_2 2<sup>nd</sup> round: Mutagenesis PCR was set up again, 1000 µL</b><br>
 +
<ul>
 +
<li>Experiment: <br>PCR according to <a href="https://2012.igem.org/Team:Goettingen/Project/Methods">protocol</a>.</li>
</ul>
</ul>
<br></td></tr>
<br></td></tr>

Revision as of 14:26, 26 September 2012

Deutsch  / English 

#3 Chemoreceptor Library - 15th Week

Back to overview

V08_06


V08_06_1 2nd round: Ethanol precipitation of mutated plasmids
  • Experiment:
    The ethanol precipitation was performed according to protocol.

V08_06_2 2nd round: Transformation of electrocompetent cells with the mutant plasmid mixture
  • Experiment:
    Electrocompetent cells were prepared according to protocol. The transformation was performed according to the established protocol.


V08_07


V08_07_1 2nd round: Analysis of transforamtion V08_06
  • Experiment:
    Plates and liquid culture were investigated.
  • Observations & Results:
    Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.

V08_07_2 2nd round: Mutagenesis PCR was set up again, 1000 µL
  • Experiment:
    PCR according to protocol.


V08_08


V08_08_1 2nd round: Analysis of transforamtion V08_06
  • Experiment:
    Plates and liquid culture were investigated.
  • Observations & Results:
    Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.

V08_08_2 2nd round: Mutagenesis PCR was set up again, 1000 µL
  • Experiment:
    PCR according to protocol.


V08_09


V08_09_1 2nd round: Analysis of transforamtion V08_06
  • Experiment:
    Plates and liquid culture were investigated.
  • Observations & Results:
    Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.

V08_09_2 2nd round: Mutagenesis PCR was set up again, 1000 µL
  • Experiment:
    PCR according to protocol.


V08_10


V08_10_1 2nd round: Analysis of transforamtion V08_06
  • Experiment:
    Plates and liquid culture were investigated.
  • Observations & Results:
    Neither the plates nor the liquid culture exhibited bacterial growth. A test gel of the ethano precipitated ligation revealed that, again, our DNA material was lost during the process.

V08_10_2 2nd round: Mutagenesis PCR was set up again, 1000 µL
  • Experiment:
    PCR according to protocol.


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