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<h4>Transforming E. Coli Rosetta and MG1655 for pRED/ET engineering</h4> | <h4>Transforming E. Coli Rosetta and MG1655 for pRED/ET engineering</h4> | ||
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Revision as of 14:44, 29 September 2018
Contents
Transforming E. Coli Rosetta and MG1655 for pRED/ET engineering
2018/08/28
Participants: | Dominic |
Protocol: | epo trafo |
Notes: | MG1655 is E.Coli WT as backup |
Results: | colonies only on MG1655 plate
No colonies on E.coli Rosetta |
8/29
pRED/ET genome engineering of delta msb-B and delta recBCD strains
Participants: | Dominic |
Protocol: | pRED/ET engineering protocol |
Notes: | the template for the resistance cassette for deletions was taken from a plasmid containing mRFP |
Results: | red colonies
Redoing the experiment but doing a dpni digest before |
8/30
Transforming E. Coli DH5a to find a reason for the contamination
Participants: | Dominic |
Protocol: | epo trafo |
Notes: | CAP_recBCD, CAP_msbb, psb1c3_mrfp in Dh5a |
Results: | red colonies on all plates -> mRFP contamination |