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<td>Participants:</td> | <td>Participants:</td> | ||
− | <td>Dominic</td> | + | <td>Dominic Schwarz</td> |
</tr> | </tr> | ||
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<td>Protocol:</td> | <td>Protocol:</td> | ||
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+ | <a href="https://static.igem.org/mediawiki/2018/c/ca/T--Munich--WL1_Electrocompetent_transformation.pdf" target="_blank">Electrocompetent transformation</a> | ||
+ | </td> | ||
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<td>Participants:</td> | <td>Participants:</td> | ||
− | <td>Dominic</td> | + | <td>Dominic Schwarz</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
<td>Protocol:</td> | <td>Protocol:</td> | ||
− | <td> | + | <td> |
+ | <a href="https://static.igem.org/mediawiki/2018/a/a5/T--Munich--WL1_Chemical_transformation.pdf" target="_blank">Chemical Transformation</a> | ||
+ | </td> | ||
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<td>Participants:</td> | <td>Participants:</td> | ||
− | <td>Dominic</td> | + | <td>Dominic Schwarz</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
<td>Protocol:</td> | <td>Protocol:</td> | ||
− | <td> | + | <td> |
+ | <a href="https://static.igem.org/mediawiki/2018/c/ca/T--Munich--WL1_Electrocompetent_transformation.pdf" target="_blank">Electrocompetent transformation</a> | ||
+ | </td> | ||
</tr> | </tr> | ||
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<td>Participants:</td> | <td>Participants:</td> | ||
− | <td>Dominic</td> | + | <td>Dominic Schwarz</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
<td>Protocol:</td> | <td>Protocol:</td> | ||
− | <td> | + | <td> |
+ | <a href="https://static.igem.org/mediawiki/2018/a/a5/T--Munich--WL1_Chemical_transformation.pdf" target="_blank">Chemical transformation</a> | ||
+ | </td> | ||
</tr> | </tr> | ||
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<td>Participants:</td> | <td>Participants:</td> | ||
− | <td>Dominic</td> | + | <td>Dominic Schwarz</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
<td>Protocol:</td> | <td>Protocol:</td> | ||
− | <td> | + | <td> |
+ | <a href="https://international.neb.com/protocols/2015/11/20/monarch-plasmid-dna-miniprep-kit-protocol-t1010" target="_blank">Mini Prep</a> | ||
+ | </td> | ||
</tr> | </tr> | ||
<tr> | <tr> |
Revision as of 20:01, 15 October 2018
Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering
2018/05/07Participants: | Dominic Schwarz |
Protocol: | Electrocompetent transformation |
Notes: | pkD3 contains resistance cassettes with FRT-sites for pRED engineering incubate pRED at 30°C because of temperature sensitive promoter pNPTS138-R6KT is for knock-ins via RecA Recombineering |
Results: | no colonies. we suspected electroporation to be a problem and tried chemical transformation of NEB Turbo next. |
Redo: Transforming E.Coli NEB Turbo to amplify plasmids for pRED/ET Engineering
2018/05/18Participants: | Dominic Schwarz |
Protocol: | Chemical Transformation |
Notes: | inoculate pRED at 30°C because of temperature sensitive promoter |
Results: | no colonies. We suspected the E. Coli NEB Turbo to be a problem and switched to E. Coli Dh5a as a cloning organism. |
Redo: Transforming E.Coli Dh5a to amplify plasmids for pRED/ET Engineering
2018/05/24Participants: | Dominic Schwarz |
Protocol: | Electrocompetent transformation |
Notes: | inoculate pRED at 30°C because of temperature sensitive promoter, pKD3 contains resistance cassette flanked by FRT sites |
Results: | no colonies |
Transforming E.Coli Dh5a to amplify plasmids for pRED/ET Engineering
2018/05/25Participants: | Dominic Schwarz |
Protocol: | Chemical transformation |
Notes: | pKD3 contains resistance cassette flanked by FRT sites |
Results: | no colonies. because pRED/ET could not be transformed, we got readily transformed cells from PD Dr. Jürgen Lassak from the LMU |
DNA preparation for pRED/ET Engineering
2018/05/26Participants: | Dominic Schwarz |
Protocol: | Mini Prep |
Notes: | because pRED/ET could not be transformed, we got readily transformed cells from PD Dr. Jürgen Lassak from the LMU |
Results: | pRED/ET: 37,5 ng/ul pNPTS138-R6KT: 60ng/ul |