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Team:Exeter/lab book/novpol/wk6
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| - | + | <!--Project Division Week Hyperlinks--> | |
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<a href="https://2012.igem.org/Team:Exeter/lab_book/novpol/wk5"; style="color:#1d1d1b">6th - 10th August</a> | <a href="https://2012.igem.org/Team:Exeter/lab_book/novpol/wk5"; style="color:#1d1d1b">6th - 10th August</a> | ||
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| - | <a href="https://2012.igem.org/Team:Exeter/ | + | <a href="https://2012.igem.org/Team:Exeter/Results/showcase"; style="color:#e30614" target="_blank"><font size="3"><b>Results</b></font></a> |
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<!--End Project Division Week Hyperlinks--> | <!--End Project Division Week Hyperlinks--> | ||
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<p>**<b>Monday 13/08/12</b>**</p><br> | <p>**<b>Monday 13/08/12</b>**</p><br> | ||
| - | <p>Added ligation mix of HAS-terminator, cyclodextran-terminator, ompA-SacB and ompA-cyclodextran to Top10 competent <i>E.coli</i> cells and <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/1" style="color:# | + | <p>Added ligation mix of HAS-terminator, cyclodextran-terminator, ompA-SacB and ompA-cyclodextran to Top10 competent <i>E.coli</i> cells and <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/1" style="color:#57b947"><u>transformed</u></a> onto ampicillin plates. </p><br> |
<p>**<b>Tuesday 14/08/12</b>**</p><br> | <p>**<b>Tuesday 14/08/12</b>**</p><br> | ||
| - | <p><a href="https://2012.igem.org/Team:Exeter/lab_book/proto/2" style="color:# | + | <p><a href="https://2012.igem.org/Team:Exeter/lab_book/proto/2" style="color:#57b947"><u>Transferred</u></a> HAS-terminator, cyclodextran-terminator, ompA-SacB and ompA-cyclodextran to liquid broth containing ampicillin.</p><br> |
<p>**<b>Wednesday 15/08/12</b>**</p><br> | <p>**<b>Wednesday 15/08/12</b>**</p><br> | ||
| - | <p>Performed <http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_k0502.pdf" style="color:# | + | <p>Performed <http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_k0502.pdf" style="color:#57b947" target="_blank"><u>mini-prep</u></a> of HAS-terminator, cyclodextran-terminator, ompA-SacB and ompA-cyclodextran. Used the nanodrop machine to confirm nucleic acid present. Digested the fragments and ran them on a gel using electrophoresis. All of the genes were single banded or absent, confirming that the ligation had not worked and only plasmid DNA was present. </p> |
<img src="https://static.igem.org/mediawiki/2012/a/a6/Exe2012_inAug_13th17th.jpg" alt="" title="" width="550" height="342"> | <img src="https://static.igem.org/mediawiki/2012/a/a6/Exe2012_inAug_13th17th.jpg" alt="" title="" width="550" height="342"> | ||
| - | <p>Used previous digestion mix of HAS, cyclo, SacB and ompA to attempt ligation again using the <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/4" style="color:# | + | <p>Used previous digestion mix of HAS, cyclo, SacB and ompA to attempt ligation again using the <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/4" style="color:#57b947"><u>3A assembly</u></a> protocol, into digested tetracycline plasmids. <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/1" style="color:#57b947"><u>Transformed</u></a> ligation mix into Top10 competent <i>E.coli </i>cells and plated out on tetracycline plates. </p><br> |
<p>**<b>Thursday 16/08/12</b>**</p><br> | <p>**<b>Thursday 16/08/12</b>**</p><br> | ||
<p>None of the plates had successfully grown any cultures so stopped lab work for the weekend.</p><br> | <p>None of the plates had successfully grown any cultures so stopped lab work for the weekend.</p><br> | ||
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| + | <p><u>Website Designed and Built by: Ryan Edginton, James Lynch & Alex Clowsley</u> | | ||
| + | <a href="https://igem.org/Team.cgi?id=764" style="color:#57B947" target="_blank"><u>Contact Us</u></a> | | ||
| + | <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 23:58, 26 September 2012
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Showcasing Polysaccharide Production: 13th - 17th August 2012 **Monday 13/08/12** Added ligation mix of HAS-terminator, cyclodextran-terminator, ompA-SacB and ompA-cyclodextran to Top10 competent E.coli cells and transformed onto ampicillin plates. **Tuesday 14/08/12** Transferred HAS-terminator, cyclodextran-terminator, ompA-SacB and ompA-cyclodextran to liquid broth containing ampicillin. **Wednesday 15/08/12** Performed 
Used previous digestion mix of HAS, cyclo, SacB and ompA to attempt ligation again using the 3A assembly protocol, into digested tetracycline plasmids. Transformed ligation mix into Top10 competent E.coli cells and plated out on tetracycline plates. **Thursday 16/08/12** None of the plates had successfully grown any cultures so stopped lab work for the weekend. |
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