Team:Exeter/lab book/3gip/wk6

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         <a href="https://2012.igem.org/Team:Exeter/lab_book/3gip/wk11"; style="color:#1d1d1b">17th - 21st September</a>
         <a href="https://2012.igem.org/Team:Exeter/lab_book/3gip/wk11"; style="color:#1d1d1b">17th - 21st September</a>
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        <a href="https://2012.igem.org/Team:Exeter/Results/inducible"; style="color:#e30614" target="_blank"><font size="3"><b>Results</b></font></a>
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       <font face="Verdana" color="#57b947" size="4">
       <p><b><u>The 3-Gene Inducible Plasmid: 13th - 17th August 2012</u></b></p>
       <p><b><u>The 3-Gene Inducible Plasmid: 13th - 17th August 2012</u></b></p>
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     <p><b><u>Monday 13th August</u></b></p>
     <p><b><u>Monday 13th August</u></b></p>
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<p>See Operon Construction: 13th - 17th August 2012</p>
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<p>See <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk6" style="color:#57B947" target="_blank"><u>Operon Construction 13th - 17th August</u></a> of RBS-<i>wbbC</i>(d) (BBa_B0034 + BBa_K764005)</p>
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<p></p><br>
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<p>https://2012.igem.org/Team:Exeter/lab_book/gibs/wk6</p><br>
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<p><b><u>Tuesday 14th August</u></b></p>
<p><b><u>Tuesday 14th August</u></b></p>
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<p>See Operon Construction: 13th - 17th August 2012</p>
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<p>See <a href="https://2012.igem.org/Team:Exeter/lab_book/gibs/wk6" style="color:#57B947" target="_blank"><u>Operon Construction 13th - 17th August</u></a> of RBS-<i>wbbC</i>(d) (BBa_B0034 + BBa_K764005)</p>
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<p></p><br>
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<p>https://2012.igem.org/Team:Exeter/lab_book/gibs/wk6</p><br>
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<p><b><u>Wednesday 15th August</u></b></p>
<p><b><u>Wednesday 15th August</u></b></p>
<p><i><b>Morning</b></i></p>
<p><i><b>Morning</b></i></p>
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<p>•<u>Mini-Prepping</u></p>  
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<p>•<a href="http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_k0502.pdf" style="color:#57B947" target="_blank"><u>Miniprepping</u></a></p>  
<p>BBa_J13002 + <i>wbnK</i> BBa_B0014 in pSB1T3</p>
<p>BBa_J13002 + <i>wbnK</i> BBa_B0014 in pSB1T3</p>
<p><i>wfcA</i> + BBa_B0014 in pSB1T3</p>
<p><i>wfcA</i> + BBa_B0014 in pSB1T3</p>
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<p>Using the changed protocol. The tubes were centrifuged for 10 minutes to start to ensure a good pellet formed. </p>
<p>Using the changed protocol. The tubes were centrifuged for 10 minutes to start to ensure a good pellet formed. </p>
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<p>After the neutralisation solution had been added, the eppindorfs were centrifuged for 10 minutes rather than 5 in order to get a better pellet formation. </p>
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<p>After the neutralisation solution had been added, the eppendorfs were centrifuged for 10 minutes rather than 5 in order to get a better pellet formation. </p>
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<p>40ul of water was added instead of 40ul in order to make sure the concentration of DNA increased. </p>
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<p>40ul of water was added instead of 50ul in order to make sure the concentration of DNA increased. </p>
<p>All were nanodropped and only <i>wfcA</i> + BBa_B0014 and <i>wbnJ</i> + BBa_B0014 gave good concentrations. </p><br>
<p>All were nanodropped and only <i>wfcA</i> + BBa_B0014 and <i>wbnJ</i> + BBa_B0014 gave good concentrations. </p><br>
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<p><b><u>Wednesday 15th August –Friday 17th August</u></b></p>
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<p><b><u>Wednesday 15th August – Friday 17th August</u></b></p>
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<p>Preparation of presentation so no lab work. </p>  
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<p>Preparation for presentation so no lab work. </p>  
      
      
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    <p><u>Website Designed and Built by: Ryan Edginton, James Lynch & Alex Clowsley</u> &nbsp;&nbsp;|&nbsp;&nbsp;
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    <a href="https://igem.org/Team.cgi?id=764" style="color:#57B947" target="_blank"><u>Contact Us</u></a>  &nbsp;&nbsp;|&nbsp;&nbsp;
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    <a href="https://2012.igem.org/Team:Exeter/site_map" style="color:#57B947"><u>Site Map</u></a></p>
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Latest revision as of 00:06, 27 September 2012

ExiGEM2012 Lab Book 3GP wk6

The 3-Gene Inducible Plasmid: 13th - 17th August 2012

Monday 13th August

See Operon Construction 13th - 17th August of RBS-wbbC(d) (BBa_B0034 + BBa_K764005)


Tuesday 14th August

See Operon Construction 13th - 17th August of RBS-wbbC(d) (BBa_B0034 + BBa_K764005)


Wednesday 15th August

Morning

Miniprepping

BBa_J13002 + wbnK BBa_B0014 in pSB1T3

wfcA + BBa_B0014 in pSB1T3

wbnJ + BBa_B0014 in pSB1T3

BBa_B0034 wbbC + BBa_B0014 in pSB1T3

Using the changed protocol. The tubes were centrifuged for 10 minutes to start to ensure a good pellet formed.

After the neutralisation solution had been added, the eppendorfs were centrifuged for 10 minutes rather than 5 in order to get a better pellet formation.

40ul of water was added instead of 50ul in order to make sure the concentration of DNA increased.

All were nanodropped and only wfcA + BBa_B0014 and wbnJ + BBa_B0014 gave good concentrations.


Wednesday 15th August – Friday 17th August

Preparation for presentation so no lab work.

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