Team:Warsaw/Calendar-Main/17 July 2008

From 2008.igem.org

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<li> Gel eloctrophoresis and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> (4300 bp band). </li>
<li> Gel eloctrophoresis and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> (4300 bp band). </li>
<li>  
<li>  
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<a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of isolated DNA fragment and Z DNA fragment isolated on 10 July. </li>
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<a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#ligation">Ligation</a> of isolated DNA fragment and Z DNA fragment isolated on <a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/14_July_2008">14 July</a>. </li>
<li> Transformation of <i>E. coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> strain with ligation. </li>
<li> Transformation of <i>E. coli</i> <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> strain with ligation. </li>
<li> Transformants plating on LB + kanamycin. </li>
<li> Transformants plating on LB + kanamycin. </li>

Revision as of 17:30, 11 October 2008

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Cloning of protein Z DNA to OmpA constructs

Michał K.

  1. Digest and dephosphorylation (with CIAP) of pACYC177+OmpA_alpha with SacI and NotI (BamHI buffer).
  2. Gel eloctrophoresis and gel-out (4300 bp band).
  3. Ligation of isolated DNA fragment and Z DNA fragment isolated on 14 July.
  4. Transformation of E. coli TOP10 strain with ligation.
  5. Transformants plating on LB + kanamycin.



Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA

Paweł

  1. Digest of pET15b-OmpA-omega and Z(in GeneArt vector) with NdeI and NotI.
  2. Gel-out of Z (~200 bp band).
  3. Overnight ligation of Z into digested pET15b-OmpA-omega.