User:Mariana Ruiz Velasco L./Notebook/IGEM 2010/Wet lab journal/2010/09/17

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Lonely day


  • In the morning, I ran a gel to check the PCR that I left yesterday. It was too bad to notice that none of the colonies showed amplification.


  • What I decided to do was to:


1. Transform (again) both click beetle luciferases. I left the plates incubating at 37°C ON.

2. Extract plasmid from several colonies during the next couple of days.