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Team:Warsaw/Calendar-Stage1/19 August 2010
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| - | <br><br><div class="note"> | + | <br><br><div class="note">Cloning Fluorescent proteins behind J23100 (without RBS) - continuation [Ania P.]</div> |
| - | <br> Repeating of transformations from friday | + | <br> Repeating of transformations from friday 16 July (because there was nothing on the plates). |
| - | <br><br><div class="note">Cloning mCherry NLS behind Anderson's RBS [Ania P., Milena, Kasia]</div> | + | <br><br><div class="note">Cloning mCherry NLS behind Anderson's RBS (Ba_J61101) [Ania P., Milena, Kasia]</div> |
<br> 1. Digest of mCherry NLS with XbaI/PstI for 3 hours. | <br> 1. Digest of mCherry NLS with XbaI/PstI for 3 hours. | ||
<br> 2. Electrophoresis (whole sample put on the gel). | <br> 2. Electrophoresis (whole sample put on the gel). | ||
Latest revision as of 20:28, 27 October 2010
Cloning Fluorescent proteins behind J23100 (without RBS) - continuation [Ania P.]
Repeating of transformations from friday 16 July (because there was nothing on the plates).
Cloning mCherry NLS behind Anderson's RBS (Ba_J61101) [Ania P., Milena, Kasia]
1. Digest of mCherry NLS with XbaI/PstI for 3 hours.
2. Electrophoresis (whole sample put on the gel).
There was not enough DNA to cut it out and isolate from agarose gel.
(zdjęcie)
