Team:SDU-Denmark/labwork/Notebook/week9

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<p> <b>27-08-2012  to  02-09-2012</b> </p>
<p> <b>27-08-2012  to  02-09-2012</b> </p>
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<CAPTION><EM>NanoDrop Results</EM></CAPTION>
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After 48 hours in the incubator, the 1-FFT colonies finaly reached a high enough concentration for sequencing.<br/><br/>
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<TR><TH>1. R0010, culture 1 <TD>18,0 ng/ul<TH>2. B0015, culture 3 <TD>67,9 ng/ul
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<TR><TH>3. B0015, , culture 5<TD>62,9 ng/ul<TH>4. R0010, culture 3 <TD>70,5 ng/ul
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Meanwhile, all the SST colonies had died out. To avoid unnecesary excess work, we simply ran PCR with all mutagenesis primers on an older 1-SST containing pJET plasmid. Miraculous, both gel band length and check digest on the resulting sequence yielded perfect results. Why had we not done this before?<br/><br/>
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In the following days 1-SST ligated into pJET, grown on ampicillin plates, transformed into Top10, transfered to liquid medium and miniprepped for sequencing.<br/>
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Latest revision as of 02:15, 27 September 2012

iGEM TEAM ::: SDU-DENMARK

Laboratory Notebook

1st week 2nd week 3rd week 4th week
5th week 6th week 7th week 8th week
9th week 10th week 11th week 12th week

27-08-2012 to 02-09-2012

After 48 hours in the incubator, the 1-FFT colonies finaly reached a high enough concentration for sequencing.

Meanwhile, all the SST colonies had died out. To avoid unnecesary excess work, we simply ran PCR with all mutagenesis primers on an older 1-SST containing pJET plasmid. Miraculous, both gel band length and check digest on the resulting sequence yielded perfect results. Why had we not done this before?

In the following days 1-SST ligated into pJET, grown on ampicillin plates, transformed into Top10, transfered to liquid medium and miniprepped for sequencing.

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