Difference between revisions of "Team:Munich/chiversions.html"
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| − | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
| − | <td></td> | + | <td>no results</td> |
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Revision as of 17:57, 16 October 2018
PCR amplify linear mtq2
2018/05/28 - 2018/05/29| Participants: | Dominic Schwarz |
| Protocol: | PCR, Agarose gel, Gel Purification |
| Notes: | VR & VF2; TA: 66° ET: 50s; Template: linear mtq2_bivtat from Lukas Aufinger (Supervisor) |
| Results: | Worked (PIC) |
Assembling Chi6(double) and Chi6-Mtq2-Chi6 by Gibson Assembly
2018/06/04 - 2018/06/08| Participants: | Dominic Schwarz |
| Protocol: | PCR, Agarose gel, Gel purification, Gibson Assembly |
| Notes: | Fragments were amplified, then purified and Gibson Assembly was performed |
| Results: | No bands were visible on the gel after Gibson Assembly, suggesting that fragments were not amplified correctly before. Additionally, we decided to do overlap PCR instead of Gibson Assembly. |
Assembling Chi6(double) and Chi6-Mtq2-Chi6 by PCR
2018/06/11 - 2018/06/14| Participants: | Dominic Schwarz |
| Protocol: | PCR, Agarose gel, Gel extraction |
| Notes: | Fragments were amplified, then purified and overlap PCR was performed. |
| Results: | The Agarose gel after overlap PCR was produced incorrectly, therefore we lost the samples. |
PCR to amplify Mtq2
2018/06/12| Participants: | Dominic Schwarz |
| Protocol: | PCR |
| Notes: | Primers: VF2, VR |
| Results: | no results |