Team:Warsaw/Calendar-Main/1 July 2008

From 2008.igem.org

(Difference between revisions)
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<li><a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation</a> of plasmids from transformants.</li>
<li><a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#plasmid_DNA_isolation">Isolation</a> of plasmids from transformants.</li>
<li>Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest"> digest</a> of plasmids with NotI.</li>
<li>Control <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest"> digest</a> of plasmids with NotI.</li>
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<li>Gel electrophoresis of digested DNA there where no proper plasmids</li>
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<li>Gel electrophoresis of digested DNA - there where no proper plasmids</li>
<li>Isolation of pZC</li>
<li>Isolation of pZC</li>

Revision as of 09:32, 16 October 2008

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Change of the reporter from pZC with B-galactosidaze to GFP or RFP

Piotr, Weronika

  1. Isolation of plasmids from transformants.
  2. Control digest of plasmids with NotI.
  3. Gel electrophoresis of digested DNA - there where no proper plasmids
  4. Isolation of pZC
  5. Isolation of nazwa (Gfp genetrator), nazwa (RFP generator)
  6. Owernight digest of nazwa (Gfp genetrator), nazwa (RFP generator) with NotI
  7. Owernight digest of pZC with NotI and defosforylation with CIAP
  8. Cloning of alpha-A and omega-A fusions on pKS

    Michał L., Ewa, Marcin

    1. Isolation of plasmids from transformants.
    2. Control digest of plasmids with SacI+NotI (BamHI buffer).
    3. Gel electrophoresis of digested DNA.

    We have successfully cloned A-alpha and A-omega fusions on pKS vector. The DNA will be now sequenced to ensure that our constructs are correct.

    Preparation of constructs with OmpA protein fusions

    Paweł

    1. Isolation of pET15b plasmid.
    2. Overnight digest of pET15b plasmid with NdeI and BamHI (Tango 2x buffer), dephosphorylation with CIAP.