Minnesota/16 July 2008
From 2008.igem.org
Revision as of 19:05, 23 July 2008 by Emartin9808 (Talk | contribs)
Back to Notebook Home | |
Go to Previous Day (July 15) | Go to Next Day (July 17) |
1. Plasmid Prep 2mL Ligated Product cultures from 07-14-2008. Follow the QIA prep and purify steps as seen in on 07-14-2008. |
2. Move Dual Promoter Plates from incubator to fridge. This will stop over growth and mutations before picking into 2mL cultures is performed later on. |
3. Transform paper DNA from iGEM notebook: (1) RFP, (2) TetR promoter, (3) Terminator, (4) MCherry. Follow iGEM handout for details on paper transformations into competent cells. |
4. Sequencing Results: Sequencing results returned poor results. Redo/rework on sequences. |