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Team:Trieste/notebook3
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<h2 class="notebook_title">Antibody</h2> | <h2 class="notebook_title">Antibody</h2> | ||
| - | + | We started testing our antibody!</br></br> | |
| + | First, we induced the expression of SIP 54.6 with IPTG (1mM) and we verified its production. We collected and lysated induced recombinant bacterial culture. After an appropriate treatment, we revolved the samples in SDS-PAGE and then we identified our protein by Western blotting. The results showed that the SIP 54.6 is present in bacterial lysates but not in surnatans. This proves that the SIP is being expressed, but not secreted. | ||
</div> | </div> | ||
<div id="chassis" class="notebook_section"> | <div id="chassis" class="notebook_section"> | ||
Revision as of 17:41, 24 September 2012
The Jolly JoCare
a safe probiotic platform for protein expression
Week 3
More
Suicide System
We inoculated the positive colonies (RBS_B0034-LL37-TT_B0015) and also checked by digestion. The construct was successfully cloned downstream the inducible promoter T5LacOperator (BBa_K875002). The M15 cells (containing the pREP4 plasmid coding for the Lac repressor) were transformed with the construct described above and seeded in Kan (M15 resistance), Cm (pSB1C3 resistance) in two conditions: with and without IPTG ( the inhibitors of the repressor Lac). Unfortunately the LL-37 cathelicidin was probably unable to disrupt the cell membrane, as we observed a growth both in induced and not induced culture.Antibody
We started testing our antibody! First, we induced the expression of SIP 54.6 with IPTG (1mM) and we verified its production. We collected and lysated induced recombinant bacterial culture. After an appropriate treatment, we revolved the samples in SDS-PAGE and then we identified our protein by Western blotting. The results showed that the SIP 54.6 is present in bacterial lysates but not in surnatans. This proves that the SIP is being expressed, but not secreted.Chassis
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