Rensselaer/22 August 2008
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(New page: '''9:00 AM Pip, James, Dimitre''' To test the different promoters for the project, we decided on using the plasmid pSB1A2 http://partsregistry.org/wiki/index.php?title=Part:pSB1A2 wh...) |
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- | To test the different promoters for the project, we decided on using the plasmid pSB1A2 [[http://partsregistry.org/wiki/index.php?title=Part:pSB1A2]] which has a RFP (red fluorescent protein) reporter. The first promoter we will test is the iron promoter from the registry [[http://partsregistry.org/wiki/index.php?title=Part:BBa_I765000]]. | + | To test the different promoters for the project, we decided on using the plasmid pSB1A2 [[http://partsregistry.org/wiki/index.php?title=Part:pSB1A2]] which has a RFP (red fluorescent protein) reporter. The first promoter we will test is the iron promoter from the registry [[http://partsregistry.org/wiki/index.php?title=Part:BBa_I765000]] on pSB1A2. |
- | The tentative schedule is that we will transform ''E. coli'' cells with the plasmids that we want to amplify Wednesday evening or Thursday morning. | + | The tentative schedule is that we will transform ''E. coli'' cells with the plasmids that we want to amplify Wednesday evening or Thursday morning. We will then do a restriction digest on the DNA to test the restriction sites on the cells ( SpeI and XbaI. |
Revision as of 19:51, 22 July 2008
9:00 AM Pip, James, Dimitre
To test the different promoters for the project, we decided on using the plasmid pSB1A2 [[1]] which has a RFP (red fluorescent protein) reporter. The first promoter we will test is the iron promoter from the registry [[2]] on pSB1A2.
The tentative schedule is that we will transform E. coli cells with the plasmids that we want to amplify Wednesday evening or Thursday morning. We will then do a restriction digest on the DNA to test the restriction sites on the cells ( SpeI and XbaI.