ArianeKrus (Talk | contribs) |
Franziwinzig (Talk | contribs) |
||
Line 28: | Line 28: | ||
<tr> | <tr> | ||
<td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> | ||
− | <td> | + | <td>Worked (PIC)</td> |
</tr> | </tr> | ||
</table> | </table> | ||
− | <h4>Assembling Chi6(double) and Chi6-Mtq2-Chi6 by | + | <h4>Assembling Chi6(double) and Chi6-Mtq2-Chi6 by Gibson Assembly</h4> |
<em>2018/06/04 - 2018/06/08</em> | <em>2018/06/04 - 2018/06/08</em> | ||
<table class="table table-borderless"> | <table class="table table-borderless"> | ||
Line 52: | Line 52: | ||
<tr> | <tr> | ||
<td>Notes:</td> | <td>Notes:</td> | ||
− | <td>Fragments were amplified, then purified and | + | <td>Fragments were amplified, then purified and Gibson Assembly was performed |
</td> | </td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
<td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> | ||
− | <td>No bands were visible on the gel after | + | <td>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.</td> |
</tr> | </tr> | ||
</table> | </table> | ||
Line 110: | Line 110: | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a>no results</td> |
<td></td> | <td></td> | ||
</tr> | </tr> |
Revision as of 17:57, 16 October 2018
PCR amplify linear mtq2
2018/05/28 - 2018/05/29Participants: | 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 - 2018/06/08Participants: | 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 - 2018/06/14Participants: | 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
2018/06/12Participants: | Dominic Schwarz |
Protocol: | PCR |
Notes: | Primers: VF2, VR |
Results:no results |