Team:Bordeaux/Third
From 2012.igem.org
ChristopheD (Talk | contribs) |
ChristopheD (Talk | contribs) |
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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> | ||
+ | |||
+ | <h4>Day 11 : 17-07-2012</h4> | ||
+ | <hr> | ||
+ | <p> | ||
+ | Day 2 of making new competent cells <a href="http://partsregistry.org/Help:Protocols/Competent_Cells" target="_blanck" class="more">Read Protocol</a> | ||
+ | </br> | ||
+ | We stopped incubating our cells at an OD600nm of 0.31 | ||
+ | </br> | ||
+ | In the end we made 192 tubes of 50μL competent cells. | ||
+ | </p> | ||
+ | |||
- | <h4>Day | + | <h4>Day 12 : 18-07-2012</h4> |
<hr> | <hr> | ||
<p> | <p> | ||
- | The competence test gave good results with a good amount of colonies on each plates and no colonies on the control plate. | + | The competence test gave good results with a good amount of colonies on each plates ( ≈ 300 ) and no colonies on the control plate. |
</br> | </br> | ||
Today we will transform DNA for every biobrick left. | Today we will transform DNA for every biobrick left. | ||
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</p> | </p> | ||
- | <h4>Day | + | <h4>Day 13 : 19-07-2012</h4> |
<hr> | <hr> | ||
<p> | <p> | ||
+ | Today we picked single colonies and put the to grow in two 5 mL LB + Ampicilin 100μg/mL | ||
+ | </br> | ||
+ | Except for 3.B who gave no colonies | ||
+ | </br> | ||
+ | We put the tubes to incubate overnight at 37°C | ||
</p> | </p> | ||
Revision as of 14:20, 23 July 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