Team:Bordeaux/Third

From 2012.igem.org

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We followed the protocol proposed by the patregistry.org <a href="http://partsregistry.org/Help:Protocols/Competent_Cells" target="_blanck" class="more">Read Protocol</a>
We followed the protocol proposed by the patregistry.org <a href="http://partsregistry.org/Help:Protocols/Competent_Cells" target="_blanck" class="more">Read Protocol</a>
</p>
</p>
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<h4>Day 11 : 17-07-2012</h4>
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<hr>
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<p>
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Day 2 of making new competent cells <a href="http://partsregistry.org/Help:Protocols/Competent_Cells" target="_blanck" class="more">Read Protocol</a>
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                                                </br>
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                                                We stopped incubating our cells at an OD600nm of 0.31
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                                                </br>
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                                                In the end we made 192 tubes of 50μL competent cells.
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</p>
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<h4>Day 11 : 18-07-2012</h4>
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<h4>Day 12 : 18-07-2012</h4>
<hr>
<hr>
<p>
<p>
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The competence test gave good results with a good amount of colonies on each plates and no colonies on the control plate.
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The competence test gave good results with a good amount of colonies on each plates ( ≈ 300 ) and no colonies on the control plate.
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</br>
Today we will transform DNA for every biobrick left.
Today we will transform DNA for every biobrick left.
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<h4>Day 12 : 19-07-2012</h4>
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<h4>Day 13 : 19-07-2012</h4>
<hr>
<hr>
<p>
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                                                Today we picked single colonies and put the to grow in two 5 mL LB + Ampicilin 100μg/mL
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                                                </br>
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                                                Except for 3.B who gave no colonies
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                                                </br>
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                                                We put the tubes to incubate overnight at 37°C
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</p>

Revision as of 14:20, 23 July 2012

Note Book - iGEM Bordeaux 2012

Day 10 : 16-07-2012


This week we decided to make our own competent cells
Regarding the bad/average results we had with our commercial DH5α and XL1blue we decided to try with DH10B strain
We followed the protocol proposed by the patregistry.org Read Protocol

Day 11 : 17-07-2012


Day 2 of making new competent cells Read Protocol
We stopped incubating our cells at an OD600nm of 0.31
In the end we made 192 tubes of 50μL competent cells.

Day 12 : 18-07-2012


The competence test gave good results with a good amount of colonies on each plates ( ≈ 300 ) and no colonies on the control plate.
Today we will transform DNA for every biobrick left.
We will use our new competent cells.

We will proceed by heat-shock as described in the partregistry.org protocol Read Protocol

Day 13 : 19-07-2012


Today we picked single colonies and put the to grow in two 5 mL LB + Ampicilin 100μg/mL
Except for 3.B who gave no colonies
We put the tubes to incubate overnight at 37°C