Team:UNIK Copenhagen/Logbook

From 2014.igem.org

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We transformed Ecloni with pETDuet-1 vector and plated the bacteria. They were afterwards stored in the fridge.<br><br>
We transformed Ecloni with pETDuet-1 vector and plated the bacteria. They were afterwards stored in the fridge.<br><br>
<b>23rd of July (Q)</b><br>We made three liquid cultures each from a single colony on the plate.<br><br>
<b>23rd of July (Q)</b><br>We made three liquid cultures each from a single colony on the plate.<br><br>
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<b>24th of July(Q)</b><br>Miniprep of the pETDuet-1 vector. The minipreps was nanodroped. The measurements were:<br></p>
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<b>24th of July(Q)</b><br>Miniprep of the pETDuet-1 vector. The minipreps was nanodroped. The measurements were:<br>
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  <td>1.68</td>
  <td>1.68</td>
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<p>On basis of the measurements, we picked sample 2 for sequencing. The sequences confirmed by sequencing.</p>
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On basis of the measurements, we picked sample 2 for sequencing. The sequences confirmed by sequencing.</p>
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Revision as of 12:39, 22 August 2014




17th of July - amplification of pETDuet-1 (Q)
We transformed Ecloni with pETDuet-1 vector and plated the bacteria. They were afterwards stored in the fridge.

23rd of July (Q)
We made three liquid cultures each from a single colony on the plate.

24th of July(Q)
Miniprep of the pETDuet-1 vector. The minipreps was nanodroped. The measurements were:

Colony: ng/µl 260/280 260/230
1 30.3 1.96 2.34
2 63.3 1.82 1.89
3 32.1 1.82 1.68

On basis of the measurements, we picked sample 2 for sequencing. The sequences confirmed by sequencing.

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