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Team:Paris Bettencourt/Experiments/Methodologies/K090403J
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After having used a replicative plasmid (pHM3), we tried to use a Bacillus subtilis integration plasmid. For that, we used and plan to continue the construction of the B.subtilis integration vector pSBINT1 built by the 2008 Cambridge iGEM team. | After having used a replicative plasmid (pHM3), we tried to use a Bacillus subtilis integration plasmid. For that, we used and plan to continue the construction of the B.subtilis integration vector pSBINT1 built by the 2008 Cambridge iGEM team. | ||
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| + | {| border="1" class="wikitable" style="text-align: center;" | ||
| + | |+T7 autoloop RFP+ Control / E-coli at 37°C | ||
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| + | |[[File:PSBINT1_final.png|290px|thumb|center|E-Coli at 37°C (trans image)]] | ||
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| + | |} | ||
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Revision as of 01:35, 22 September 2011
After having used a replicative plasmid (pHM3), we tried to use a Bacillus subtilis integration plasmid. For that, we used and plan to continue the construction of the B.subtilis integration vector pSBINT1 built by the 2008 Cambridge iGEM team.
{| border="1" class="wikitable" style="text-align: center;"
|+T7 autoloop RFP+ Control / E-coli at 37°C
|-
|[[File:PSBINT1_final.png|290px|thumb|center|E-Coli at 37°C (trans image)]]
|}
