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Team:Penn/Notebook/DrugDelivery
From 2012.igem.org
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'''Wet Lab''' | '''Wet Lab''' | ||
| - | + | We PCR'ed out mCherry from the NAS 151 plasmid. Following this we did a gel purification which resulted in a 30ns/<math>lambda</math> yield. | |
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| + | == '''06/12/2012''' == | ||
| + | '''Wet Lab''' | ||
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| + | We transformed pCyA and HO1 | ||
Revision as of 16:53, 26 June 2012
Contents |
06/07/2012
Wet Lab
Today we transformed both versions of cph8 from 2012 Distribution.
Dry Lab
We also placed order for the following new BioBricks:
- BBa_K207001 - PhyB-DBD Fusion
- BBa_K422012 - Pif3 (Aar1 C part)
- BBa_K422013 - PhyB (Aar1 C part)
- BBa_K592006 - pFixK2
- BBa_K592004 - YF1
- BBa_K592005 - FixJ
- BBa_K592000 - Cph8
- BBa_K365000 - Pif3
In addition, we brainstormed and developed a new idea to use the PYP/GCN system to activate a gene.
06/08/2012
Wet Lab
No colonies appeared in the transformation of both cph8 a/b. We suspect that the failure of the transformatiosns were due to bad sequences.
06/11/2012
Wet Lab
We PCR'ed out mCherry from the NAS 151 plasmid. Following this we did a gel purification which resulted in a 30ns/<math>lambda</math> yield.
06/12/2012
Wet Lab
We transformed pCyA and HO1
