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<td>Notes:</td> | <td>Notes:</td> | ||
− | <td> | + | <td>We also inoculated LB media blindly.</td> |
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<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>No colonies, no growth; <br> |
We decided to use a resistance cassette from pSB1C3 without FRT sites | We decided to use a resistance cassette from pSB1C3 without FRT sites | ||
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<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>PIC. | + | <td>PIC. We thought the band might be what we wanted but because of how few DNA the extraction yielded, these samples were not used in further experiments. |
</td> | </td> | ||
</tr> | </tr> |
Revision as of 19:17, 16 October 2018
Transforming E. Coli DH5a to amplify pKD3 for pRED/ET engineering
2018/05/28Participants: | Dominic Schwarz |
Protocol: | Electrocompetent transformation |
Notes: | We also inoculated LB media blindly. |
Results: | No colonies, no growth; We decided to use a resistance cassette from pSB1C3 without FRT sites |
Amplifying a selection cassette from pSB1C3
2018/05/29Participants: | Enikö Baligács |
Protocol: | PCR, Agarose gel, Gel extraction |
Notes: | Primer with 50bp homology regions ????, TA: 67°C, Elongation: 45s |
Results: | PIC. We thought the band might be what we wanted but because of how few DNA the extraction yielded, these samples were not used in further experiments. |