Team:Warsaw/Calendar-Main/10 October 2008

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<li> Tranformants planting on LB with kanamycin. </li>
<li> Tranformants planting on LB with kanamycin. </li>
<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>Isolation</a> of plasmid from culture inoculated on previous day - <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pMPM-T5-AID>pMPMT5+AID</a> without EcoRI site.</li>
<li><a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation>Isolation</a> of plasmid from culture inoculated on previous day - <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pMPM-T5-AID>pMPMT5+AID</a> without EcoRI site.</li>
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<li>Control <a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>digest</a> of isolated plasmids with EcoRI and BamHI (BamHI buffer) - proper clones found.</li>
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</ol>
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<h3></h3>
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<h4>Michał K.</h4>
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<ol>

Revision as of 15:01, 25 October 2008

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Visit in US Embassy

Visas have been accorded to the whole team.

Preparation of BioBricks

Michał K.

  1. Digest of RFP(?????)+deltaA with EcoRI and SacI (BamHI buffer), dephosphorylation with CIAP
  2. Gel electrophoresis and gel-out of proper band 2200 bp.
  3. Ligation of digested 5kb (??????) vector from (30 September) with pT7_omega_link and RFP(?????) with pT7_alpha fragment (1 hr).
  4. PCR on pACYC177+OmpA_omega_deltaA_alpha plasmid using AlphaL+Nde and AlphaP+link10+homo2 primers (annealing temperature 58 °C; elongation length 60s) to obtain alpha fragment.
  5. Gel electrophoresis and gel-out of proper band 600 bp.

Piotr

  1. Transformation of TOP10 with above ligations.
  2. Tranformants planting on LB with kanamycin.
  3. Isolation of plasmid from culture inoculated on previous day - pMPMT5+AID without EcoRI site.
  4. Control digest of isolated plasmids with EcoRI and BamHI (BamHI buffer) - proper clones found.

Michał K.