Team:Groningen/Notebook/Wetwork 14September2012

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Tom<br>
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Restriction and ligation of constructs and linearized psb1c3 for submitting of parts.<br>
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3 constructs of alsT with amilgfp, amilcp and lycopene in psb1c3. 3 constructs of fnr with amilgfp, amilcp and lycopene in psb1c3. 4 constructs of sboA with 2x amilgfp,amilcp and lycopene in psb1c3.<br>
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Transformation in <i>E. coli</i> did not work probably due to bad competent cells.<br> <br>
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Nisa <br><br>
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Plasmid isolation results: some E. coli containing volatile detection device showed very strong colour. We also isolated positive control of GFP expression that has been provided by Jeroen (rrnB promoter+GFP)<br> <br>
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Cloned strong promoter rrnB to pSac-Cm+GFP opt. <br>
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  <A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A>
  <A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A>

Latest revision as of 15:11, 26 September 2012







Tom

Restriction and ligation of constructs and linearized psb1c3 for submitting of parts.
3 constructs of alsT with amilgfp, amilcp and lycopene in psb1c3. 3 constructs of fnr with amilgfp, amilcp and lycopene in psb1c3. 4 constructs of sboA with 2x amilgfp,amilcp and lycopene in psb1c3.
Transformation in E. coli did not work probably due to bad competent cells.

Nisa

Plasmid isolation results: some E. coli containing volatile detection device showed very strong colour. We also isolated positive control of GFP expression that has been provided by Jeroen (rrnB promoter+GFP)

Cloned strong promoter rrnB to pSac-Cm+GFP opt.

Back to notebook