http://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&feed=atom&action=historyTeam:Groningen/international cooperation - Revision history2024-03-28T22:10:13ZRevision history for this page on the wikiMediaWiki 1.16.0http://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=296346&oldid=prevElbrich at 02:42, 27 October 20122012-10-27T02:42:53Z<p></p>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"> <z2> iGEM Cambridge</z2></ins></div></td></tr>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"> At the European Jamboree we got in contact with the Cambridge team. Since they work on <i>Bacillus subtilis</i> too, we have quite a few things in common. Cambridge uses the magnificient ability of our favourite bacterium to form spores to store their sensor system. <br><br></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">Since the Cambridge team had trouble with their sporulation protocol, we provided the Cambridge team with our protocols and some tips & tricks for sporulation. Luckily this gave them higher yielding spores in the last weeks! We also were really happy to discuss the topic of germination with them. </ins></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <z2>Characterization of <i>B.subtilis</i> plasmid backbone created by iGEM LMU Munich 2012</z2></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <z2>Characterization of <i>B.subtilis</i> plasmid backbone created by iGEM LMU Munich 2012</z2></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> Prof. Papin, supervisor to the iGEM Virginia team and supervising author to the idFBA article, graciously shared his knowledge and scripts relating to </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> Prof. Papin, supervisor to the iGEM Virginia team and supervising author to the idFBA article, graciously shared his knowledge and scripts relating to </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> idFBA.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> idFBA.</div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"> <z2> iGEM Cambridge</z2></del></div></td><td colspan="2"> </td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;"> At the European Jamboree we got in contact with the Cambridge team. Since they work on <i>Bacillus subtilis</i> too, we have quite a few things in common. Cambridge uses the magnificient ability of our favourite bacterium to form spores to store their sensor system. <br><br></del></div></td><td colspan="2"> </td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del style="color: red; font-weight: bold; text-decoration: none;">Since the Cambridge team had trouble with their sporulation protocol, we provided the Cambridge team with our protocols and some tips & tricks for sporulation. Luckily this gave them higher yielding spores in the last weeks! We also were really happy to discuss the topic of germination with them. </del></div></td><td colspan="2"> </td></tr>
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</table>Elbrichhttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=293823&oldid=prevRenskevR at 01:00, 27 October 20122012-10-27T01:00:47Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><br><br> After the European Jamboree, the Uppsala team sent us the red chromoprotein eforRed (BBa_K592012). Although we could prove succesful cloning into our plasmid psac-cm connected to our promoter P<i>sboaA</<del class="diffchange diffchange-inline">o</del>>, into <i>E. coli</i> and <i>Bacillus subtilis</i> by restriction analysis, there was no visible expression of the protein.</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><br><br> After the European Jamboree, the Uppsala team sent us the red chromoprotein eforRed (BBa_K592012). Although we could prove succesful cloning into our plasmid psac-cm connected to our promoter P<i>sboaA</<ins class="diffchange diffchange-inline">i</ins>>, into <i>E. coli</i> and <i>Bacillus subtilis</i> by restriction analysis, there was no visible expression of the protein.</div></td></tr>
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</table>RenskevRhttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=293807&oldid=prevRenskevR at 01:00, 27 October 20122012-10-27T01:00:13Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> and managed to turn <i>B.subtilis</i> into blue and yellow, which has never been done before! </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> and managed to turn <i>B.subtilis</i> into blue and yellow, which has never been done before! </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><br><br> After the European Jamboree, the Uppsala team sent us the red chromoprotein eforRed (BBa_K592012). Although we could prove succesful cloning into our plasmid psac-cm connected to our promoter P<i>sboaA</o>, into <i>E. coli</i> and <i>Bacillus subtilis</i> by restriction analysis, there was no visible expression of the protein.</ins></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> Prof. Papin, supervisor to the iGEM Virginia team and supervising author to the idFBA article, graciously shared his knowledge and scripts relating to </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> Prof. Papin, supervisor to the iGEM Virginia team and supervising author to the idFBA article, graciously shared his knowledge and scripts relating to </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> idFBA.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> idFBA.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"> </p></ins></div></td></tr>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"> <z2> iGEM Cambridge</z2></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"> <br></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"> <br></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"> At the European Jamboree we got in contact with the Cambridge team. Since they work on <i>Bacillus subtilis</i> too, we have quite a few things in common. Cambridge uses the magnificient ability of our favourite bacterium to form spores to store their sensor system. <br><br></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;">Since the Cambridge team had trouble with their sporulation protocol, we provided the Cambridge team with our protocols and some tips & tricks for sporulation. Luckily this gave them higher yielding spores in the last weeks! We also were really happy to discuss the topic of germination with them. </ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td></tr>
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</table>RenskevRhttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=292842&oldid=prevTomvanlente at 00:09, 27 October 20122012-10-27T00:09:46Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> We characterized this plasmid backbone by doing a <del class="diffchange diffchange-inline">simple </del>growth experiment on a starch agar plate. <i>B. subtilis</i> </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> We characterized this plasmid backbone by doing a growth experiment on a starch agar plate. <i>B. subtilis</i> </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> strains (168 wildtype, pSac-Cm, and K823023, clockwise respectively) were inoculated in LB agar+0.4% starch and incubated overnight </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> strains (168 wildtype, pSac-Cm, and K823023, clockwise respectively) were inoculated in LB agar+0.4% starch and incubated overnight </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> in 37<sup>o</sup>C (left picture). After the addition of 0.1% iodine, a clear zone was formed around <i>B. subtilis</i> </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> in 37<sup>o</sup>C (left picture). After the addition of 0.1% iodine, a clear zone was formed around <i>B. subtilis</i> </div></td></tr>
</table>Tomvanlentehttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=221318&oldid=prevTomvanlente at 22:35, 26 September 20122012-09-26T22:35:48Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> The iGEM team LMU Munich 2012 has developed a plasmid backbone that is suitable for gene expression in <i>B. subtilis</i> <b>(BBa_K823023)</b>. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> The iGEM team LMU Munich 2012 has developed a plasmid backbone that is suitable for gene expression in <i>B. subtilis</i> <b>(BBa_K823023)</b>. </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> This plasmid backbone contains an integration locus in amyE, which means after being transformed into <i>B. subtilis</i>, </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> This plasmid backbone contains an integration locus in amyE, which means <ins class="diffchange diffchange-inline">that </ins>after being transformed into <i>B. subtilis</i>, </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> the cloned insert will be integrated with <i>B. subtilis</i> genome at the amyE locus. <i>B. subtilis</i> is known for its </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> the cloned insert will be integrated with <ins class="diffchange diffchange-inline">the </ins><i>B. subtilis</i> genome at the amyE locus. <i>B. subtilis</i> is known for its </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> starch degrading ability and amyE is a gene responsible for the starch degradation phenotype in <i>B.subtilis</i> by regulating a-amylase production. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> starch degrading ability and amyE is a gene responsible for the starch degradation phenotype in <i>B.subtilis</i> by regulating a-amylase production. </div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> We characterized this plasmid backbone by doing a simple growth experiment on a starch agar plate. <i>B. subtilis</i> </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> We characterized this plasmid backbone by doing a simple growth experiment on a starch agar plate. <i>B. subtilis</i> </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> strains (168 wildtype, pSac-Cm, and K823023, clockwise respectively) were inoculated in LB agar+0.4% starch and incubated overnight </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> strains (168 wildtype, pSac-Cm, and K823023, clockwise respectively) were inoculated in LB agar+0.4% starch and incubated overnight </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> in 37<sup>o</sup>C (left picture). After the addition of 0.1% iodine, <del class="diffchange diffchange-inline">the </del>clear zone was formed around <i>B. subtilis</i> </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> in 37<sup>o</sup>C (left picture). After the addition of 0.1% iodine, <ins class="diffchange diffchange-inline">a </ins>clear zone was formed around <i>B. subtilis</i> </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> wildtype and <i>B. subtilis</i> strain containing pSac-Cm. There was no clear zone observed around</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> wildtype and <i>B. subtilis</i> strain containing pSac-Cm. There was no clear zone observed around</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <i>B. subtilis</i> strain containing backbone K823023 (right picture).</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <i>B. subtilis</i> strain containing backbone K823023 (right picture).</div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> At the beginning of August we received the chromoproteins amilCP (blue), amilGFP (yellow) from</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> At the beginning of August we received the chromoproteins amilCP (blue), amilGFP (yellow) from</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <a class="inlink" href="https://2011.igem.org/Team:Uppsala-Sweden">iGEM Uppsala 2011</a>. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <a class="inlink" href="https://2011.igem.org/Team:Uppsala-Sweden">iGEM Uppsala 2011</a>. </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> We were able to transform their BBa_K592009 and BBa_K592010 behind our identified promoters into <i>E.coli</i><del class="diffchange diffchange-inline">. </del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> We were able to transform their BBa_K592009 and BBa_K592010 behind our identified promoters into <i>E.coli</i> </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> <del class="diffchange diffchange-inline">And </del>managed to turn <i>B.subtilis</i> into blue and yellow, which has never been done before! </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> <ins class="diffchange diffchange-inline">and </ins>managed to turn <i>B.subtilis</i> into blue and yellow, which has never been done before! </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> Emily Hicks from the winning Calgary iGEM team in 2011, and now member of iGEM Calgary 2012, has studied in Groningen during her exchange period. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> Emily Hicks from the winning Calgary iGEM team in 2011, and now member of iGEM Calgary 2012, has studied in Groningen during her exchange period. </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> She was very interested in her iGEM Groningen colleagues; therefore we asked her to give a lecture about her previous iGEM experience. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> She was very interested in her iGEM Groningen colleagues; therefore we asked her to give a lecture about her previous iGEM experience. </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> We were really motivated by Emily's <del class="diffchange diffchange-inline">tips </del>concerning medal requirements, information about wiki etc. Thank you Emily!</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> We were really motivated by Emily's <ins class="diffchange diffchange-inline">suggestions </ins>concerning medal requirements, information about wiki etc. Thank you Emily!</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td></tr>
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</table>Tomvanlentehttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=208603&oldid=prevAlicja at 18:17, 26 September 20122012-09-26T18:17:05Z<p></p>
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</table>Alicjahttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=194589&oldid=prevElbrich at 12:13, 26 September 20122012-09-26T12:13:19Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <a class="inlink" href="https://2011.igem.org/Team:Uppsala-Sweden">iGEM Uppsala 2011</a>. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <a class="inlink" href="https://2011.igem.org/Team:Uppsala-Sweden">iGEM Uppsala 2011</a>. </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> We were able to transform their BBa_K592009 and BBa_K592010 behind our identified promoters into <i>E.coli</i>. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> We were able to transform their BBa_K592009 and BBa_K592010 behind our identified promoters into <i>E.coli</i>. </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> And managed to turn >B.subtilis</i> into blue and yellow, which has never been done before! </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> And managed to turn <ins class="diffchange diffchange-inline"><i</ins>>B.subtilis</i> into blue and yellow, which has never been done before! </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> For the latest results, check our <a class="inlink" href="https://2012.igem.org/Team:Groningen/pigmentproduction">Pigment page</a>.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td></tr>
</table>Elbrichhttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=182107&oldid=prevJparrish at 21:59, 25 September 20122012-09-25T21:59:03Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> <z2>Characterization of <del class="diffchange diffchange-inline"> </del><i><del class="diffchange diffchange-inline">Bacillus </del>subtilis</i> plasmid <del class="diffchange diffchange-inline"> </del>backbone created by <del class="diffchange diffchange-inline"> </del>iGEM LMU Munich 2012</z2></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> <z2>Characterization of <i><ins class="diffchange diffchange-inline">B.</ins>subtilis</i> plasmid backbone created by iGEM LMU Munich 2012</z2></div></td></tr>
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</table>Jparrishhttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=182098&oldid=prevJparrish at 21:58, 25 September 20122012-09-25T21:58:16Z<p></p>
<a href="http://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=182098&oldid=177982">Show changes</a>Jparrishhttp://2012.igem.org/wiki/index.php?title=Team:Groningen/international_cooperation&diff=177982&oldid=prevElbrich at 18:31, 25 September 20122012-09-25T18:31:32Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> At the beginning of August we received the chromoproteins amilCP (blue), amilGFP (yellow) from</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> At the beginning of August we received the chromoproteins amilCP (blue), amilGFP (yellow) from</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <A HREF="https://2011.igem.org/Team:Uppsala-Sweden" TARGET="_blank"><FONT COLOR=#ff6700>iGEM Uppsala 2011</FONT></A>. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> <A HREF="https://2011.igem.org/Team:Uppsala-Sweden" TARGET="_blank"><FONT COLOR=#ff6700>iGEM Uppsala 2011</FONT></A>. </div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> We were able to transform their BBa_K592009 and BBa_K592010 behind our identified promoters into <i>E.coli</i>. And managed to turn >B.subtilis</i> into blue and yellow, which has never been done before! For the latest results, check our <A HREF="https://2012.igem.org/Team:Groningen/<del class="diffchange diffchange-inline">Pigments</del>" TARGET="_blank"><FONT COLOR=#ff6700>Pigment page</FONT></A>.</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div> We were able to transform their BBa_K592009 and BBa_K592010 behind our identified promoters into <i>E.coli</i>. And managed to turn >B.subtilis</i> into blue and yellow, which has never been done before! For the latest results, check our <A HREF="https://2012.igem.org/Team:Groningen/<ins class="diffchange diffchange-inline">pigmentproduction</ins>" TARGET="_blank"><FONT COLOR=#ff6700>Pigment page</FONT></A>.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div> </p></div></td></tr>
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</table>Elbrich