Difference between revisions of "Team:Munich/recbcdwt.html"
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>1,2,4 worked | <td>1,2,4 worked | ||
3,5,6 didnt PIC</td> | 3,5,6 didnt PIC</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>1,2,4,6 worked (PIC)</td> | <td>1,2,4,6 worked (PIC)</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>no colonies?</td> | <td>no colonies?</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>Gel PIC</td> | <td>Gel PIC</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>We lost the samples during agarose gel verification because the loading dye was contaminated. Redoing the experiment with Thomas (supervisor) yielded no colonies. Eni decided to go to a different lab because cloning doesnt work at the simmel lab. We therefore went to Prof. Gil Westmeyer at the Helmholtz Zentrum and continued our work there.</td> | <td>We lost the samples during agarose gel verification because the loading dye was contaminated. Redoing the experiment with Thomas (supervisor) yielded no colonies. Eni decided to go to a different lab because cloning doesnt work at the simmel lab. We therefore went to Prof. Gil Westmeyer at the Helmholtz Zentrum and continued our work there.</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>?</td> | <td>?</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>Colonies for pSB1C3_RecBCD(WT), no colonies for pSB1C3_RecBCD-His</td> | <td>Colonies for pSB1C3_RecBCD(WT), no colonies for pSB1C3_RecBCD-His</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>no colonies for pSB1C3_RecBCD-His</td> | <td>no colonies for pSB1C3_RecBCD-His</td> | ||
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| − | <td>Results:</td> | + | <td><a href="https://2018.igem.org/Team:Munich/Results" target="_blank">Results:</a></td> |
<td>sequencing didnt give reads, but because eurofins had problems we prepared new DNA and told them to do it again. results?. sequencial test-PCR showed a correctly assembled plasmid of recBCD(WT) (PIC)</td> | <td>sequencing didnt give reads, but because eurofins had problems we prepared new DNA and told them to do it again. results?. sequencial test-PCR showed a correctly assembled plasmid of recBCD(WT) (PIC)</td> | ||
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Revision as of 14:07, 16 October 2018
Assembling pSB1C3_RecBCD(WT) with gibson assembly
2018/08/06| Participants: | Enikö Baligács, Katja Neishsalo |
| Protocol: | PCR, Agarose gel, Gel purification, Gibson assembly, Chemical transformation |
| Notes: |
BB & LacO
Primer: GA_lacO_rv & GA_lact_fw
expect: 2,5 kb RecC-UTR for GA GA_RecC_fw & GA_RecB_rv expect: 3,5 kb RecB/D for GA GA_RecB_fw & GA_RecD_rv expect: 5,3 kb; repeated because didnt work BB & LacO for GG SapI Lact_His_SapI_fw & RecC_lacO_His_SapI_rv expect: 2,5 kb RecB/D-His for GG RecD_His_SapI_rv & RecB_His_SapI_rv expect: 5,3 kb repeated because didnt work RecC-His for GG RecB-RecC-UTR_SapI_rv & RecC_His_SapI_fw expect: 3,5 kb repeated because didnt work TM: all 60 ° |
| Results: | 1,2,4 worked 3,5,6 didnt PIC |
redo: Assembling pSB1C3_RecBCD(WT) with gibson assembly
2018/08/08| Participants: | Enikö Baligács, Katja Neishsalo |
| Protocol: | PCR, Agarose gel, Gel purification, Gibson assembly, Chemical transformation |
| Notes: |
BB & LacO
Primer: GA_lacO_rv & GA_lact_fw
expect: 2,5 kb RecC-UTR for GA GA_RecC_fw & GA_RecB_rv expect: 3,5 kb RecB/D for GA GA_RecB_fw & GA_RecD_rv expect: 5,3 kb; repeated because didnt work BB & LacO for GG SapI Lact_His_SapI_fw & RecC_lacO_His_SapI_rv expect: 2,5 kb RecB/D-His for GG RecD_His_SapI_rv & RecB_His_SapI_rv expect: 5,3 kb repeated because didnt work RecC-His for GG RecB-RecC-UTR_SapI_rv & RecC_His_SapI_fw expect: 3,5 kb repeated because didnt work TM: all 60 ° |
| Results: | 1,2,4,6 worked (PIC) |
DNA mini-preparation of pSB1C3_mRFP
2018/08/09| Participants: | Enikö Baligács |
| Protocol: | Mini Prep |
testing pSB1C3_RecBCD(WT) toxicity in cells
2018/08/13| Participants: | Katja Neishsalo |
| Protocol: | Chemical transformation, Gibson assembly, Agarose gel |
| Notes: | to improve cell survival we added 1% glucose to lb media |
| Results: | no colonies? |
Genomic extraction of RecBC fragment
2018/08/14| Participants: | Katja Neishsalo |
| Protocol: | Restriction digest |
| Notes: | Primers |
| Results: | Gel PIC |
redo: Assembling pSB1C3_RecBCD(WT) with gibson assembly
2018/08/14| Participants: | Enikö Baligács, Katja Neishsalo |
| Protocol: | PCR, Agarose gel, Gel purification, Gibson assembly, Chemical transformation |
| Notes: |
BB & LacO
Primer: GA_lacO_rv & GA_lact_fw
expect: 2,5 kb RecC-UTR for GA GA_RecC_fw & GA_RecB_rv expect: 3,5 kb RecB/D for GA GA_RecB_fw & GA_RecD_rv expect: 5,3 kb; repeated because didnt work BB & LacO for GG SapI Lact_His_SapI_fw & RecC_lacO_His_SapI_rv expect: 2,5 kb RecB/D-His for GG RecD_His_SapI_rv & RecB_His_SapI_rv expect: 5,3 kb repeated because didnt work RecC-His for GG RecB-RecC-UTR_SapI_rv & RecC_His_SapI_fw expect: 3,5 kb repeated because didnt work TM: all 60 ° |
| Results: | We lost the samples during agarose gel verification because the loading dye was contaminated. Redoing the experiment with Thomas (supervisor) yielded no colonies. Eni decided to go to a different lab because cloning doesnt work at the simmel lab. We therefore went to Prof. Gil Westmeyer at the Helmholtz Zentrum and continued our work there. |
preparing different pSB backbones
2018/08/20| Participants: | Julia Mayer, Thomas Frank |
| Protocol: | PCR, Agarose gel, Gel extraction |
| Notes: | |
| Results: | ? |
Assembling pSB1C3_RecBCD(WT) with gibson assembly
2018/08/27| Participants: | Enikö Baligács |
| Protocol: | PCR, Agarose gel, Gel purification, Gibson assembly, Chemical transformation |
| Notes: | RecBD: RecD_extract_fw & RecB_extract_rv Template: genomic DNA (54,5 ng/µl) RecC: RecC_extract_fw & RecC_extract_rv Template: genomic DNA (54,5 ng/µl) BB & LacO Primer: GA_lacO_rv & GA_lact_fw expect: 2,5 kb RecC-UTR for GA GA_RecC_fw & GA_RecB_rv expect: 3,5 kb RecB/D for GA GA_RecB_fw & GA_RecD_rv expect: 5,3 kb; repeated because didnt work BB & LacO for GG SapI Lact_His_SapI_fw & RecC_lacO_His_SapI_rv expect: 2,5 kb RecB/D-His for GG RecD_His_SapI_rv & RecB_His_SapI_rv expect: 5,3 kb repeated because didnt work RecC-His for GG RecB-RecC-UTR_SapI_rv & RecC_His_SapI_fw expect: 3,5 kb repeated because didnt work TM: all 60 ° |
| Results: | Colonies for pSB1C3_RecBCD(WT), no colonies for pSB1C3_RecBCD-His |
Redo: Assembling pSB1C3_RecBCD-His
2018/08/29| Participants: | Enikö Baligács |
| Protocol: | PCR, Agarose gel, Gel purification, Gibson assembly, Chemical transformation |
| Notes: | Primers??; We used T4 ligase instead of quick ligase like before. We added GC-buffer to the PCR reaction |
| Results: | no colonies for pSB1C3_RecBCD-His |
sequencing pSB1C3_RecBCD(WT)
2018/08/30| Participants: | Enikö Baligács |
| Protocol: | Mini Prep, Sequencing, PCR |
| Notes: | |
| Results: | sequencing didnt give reads, but because eurofins had problems we prepared new DNA and told them to do it again. results?. sequencial test-PCR showed a correctly assembled plasmid of recBCD(WT) (PIC) |