Team:Trieste/notebook6

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    <h2 class="notebook_title">Antibody</h2>
    <h2 class="notebook_title">Antibody</h2>
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The sequences arrived, and both scFv versions (pelB-scFv and LPP-scFv) are correct, so we continued with our work. Afer different attempts, we finally ligated both scFv versions under T5LacO. We amplified the resulting plasmid in DH5L and introduced it into W3110 (with p-REP 4) which we will use for future analysis.
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    <div id="chassis" class="notebook_section">
    <div id="chassis" class="notebook_section">

Revision as of 17:44, 24 September 2012

Week 6

More

Suicide System

Holin is defined as a Bglbrick part, that means it doesn't have the standard restriction sites. We transformed the standard Biobrick we needed to use, in Bglbrick by PCR.

The promoter T5CumateOperator(BBa_K875001) was cut EcoRI/SpeI, the fragment was eluted from the gel and then cloned upstream the RBS_B0034, into the pSB1A2 linearized backbone.

We screened the colonies by PCR with the standard VF2 and VR primers and the positive ones were inoculated; we amplified the miniprep by PCR with particular primers with the EcoRI, BglII, BamHI and XhoI restriction sites.

Antibody

The sequences arrived, and both scFv versions (pelB-scFv and LPP-scFv) are correct, so we continued with our work. Afer different attempts, we finally ligated both scFv versions under T5LacO. We amplified the resulting plasmid in DH5L and introduced it into W3110 (with p-REP 4) which we will use for future analysis.

Chassis

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Università degli studi di Trieste ICGEB Illy Fondazione Cassa di Risparmio
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