Difference between revisions of "Team:UGent Belgium/LabNotebook"

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        <a data-toggle="collapse" href="#September">September</a>
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        <li class="list-group-item borderless"><b>September 29:</b> <p>
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We made a strong expression vector (pXS) by restriction of the linearized plasmid backbone pSB1C3 and insertion of gblock made up of promoter-RBS-cloning site-terminator-terminator (cut with EcoRI and PstI).
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              Our first attempts to isolate the inaZ gene from <i>P. syringae</i> and the inaX gene from <i>X. campestris</i> failed.
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Revision as of 20:15, 6 October 2016

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Lab Notebook

August

  • August 29:

    • We made a strong expression vector (pXS) by restriction of the linearized plasmid backbone pSB1C3 and insertion of gblock made up of promoter-RBS-cloning site-terminator-terminator (cut with EcoRI and PstI).
    • Our first attempts to isolate the inaZ gene from P. syringae and the inaX gene from X. campestris failed.
  • August 30:

    • We transformed the strong expression vector (cf. 29/08) by electroshock into E. coli TOP10.
    • As a backup strategy we also used CPEC with the backbone from the K584027 plasmid to generate a strong expression vector.
  • August 31:

    • Second attempt to isolate the inaZ gene from P. syringae and the inaX gene from X. campestris. InaX failed, but inaZ was successful.
    • Transformation of the strong expression vector by restriction and ligation was not very successful, we only had a few colonies. The backbone amplification using CPEC was successful (cf. 30/08).

September

  • September 29:

    • We made a strong expression vector (pXS) by restriction of the linearized plasmid backbone pSB1C3 and insertion of gblock made up of promoter-RBS-cloning site-terminator-terminator (cut with EcoRI and PstI).
    • Our first attempts to isolate the inaZ gene from P. syringae and the inaX gene from X. campestris failed.