Team:Fatih Turkey/Experiments2

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     <td width="600" height="223" valign="top"><p><strong>THE SUICIDE EXPERIMENT OF E. COLI</strong><br />
     <td width="600" height="223" valign="top"><p><strong>THE SUICIDE EXPERIMENT OF E. COLI</strong><br />
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           <em>Our K541545 part contains IPTG promoter and the gene  part of LALF protein on a backbone which has resistance to chloramphenicol. We  transported this part to E. coli for testing whether E. coli would stop its own  growth like a suicide.</em> <br />
           <em>Our K541545 part contains IPTG promoter and the gene  part of LALF protein on a backbone which has resistance to chloramphenicol. We  transported this part to E. coli for testing whether E. coli would stop its own  growth like a suicide.</em> <br />
           <strong>Assays of plates with and without IPTG</strong> <br />
           <strong>Assays of plates with and without IPTG</strong> <br />
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Latest revision as of 20:07, 28 October 2011

deneme baslik

THE SUICIDE EXPERIMENT OF E. COLI


Our K541545 part contains IPTG promoter and the gene part of LALF protein on a backbone which has resistance to chloramphenicol. We transported this part to E. coli for testing whether E. coli would stop its own growth like a suicide.
Assays of plates with and without IPTG
Assay 1: We streaked E. coli culture which has BBa_K541545. Media also included chloramphenicol and IPTG. As a control group, a plate that has no IPTG is prepared. We aimed to see less colonies comparing with control group.
Assay 2: This experiment was done in order to eliminate the possibility of toxic effect of IPTG. E.coli without IPTG promoter was streaked a plate that does not have IPTG. For a second plate, E.coli with PlacI promoter was added into plate with IPTG.