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Team:Tianjin/Notebook
From 2012.igem.org
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==July 14th, 2012== | ==July 14th, 2012== | ||
| - | #Transform two plasmids of we got yestday together into E.coli.[[File:TJU2012-Note-gen-3.png|center|Gene 3]] | + | #Transform two plasmids of we got yestday together into E.coli.[[File:TJU2012-Note-gen-3.png|center|500px|Gene 3]] |
#PCR verification of colonies on the LB plates. | #PCR verification of colonies on the LB plates. | ||
#Inculcated the right colonies in Liquid LB. | #Inculcated the right colonies in Liquid LB. | ||
Revision as of 18:44, 25 September 2012
July 6th, 2012
- We discuss our all of the possible projects, and finally choose one. And then allocate works to specific member.
- Do some pre-experiment and make some reagants.
- Liquid LB
- 10g tryptone
- 5g yeast extract
- 10g NaCl
- Solid LB
- 10g tryptone
- 5g yeast extract
- 10g NaCl
- 20g agar
- Liquid LB
- Cleaned up the lab and laboratory instruments
July 8th, 2012
- Solutions for extracting plasmid.
- 50mM Glucose / 25mM Tris-Cl / 10mM EDTA，pH=8.0
- 0.2N NaOH / 1% SDS
- 3M KOAc / 2M HOAc
- Experiment technologies training, such as making gel, gel electrophoresis.
July 11th, 2012
- Designed primers and sent orders.
- Optimized the project and allocated work.
- Experiment technologies and knowledge training
- PCR principle and operation
- Gel Extraction
July 13th, 2012
1. Received the oligo and began to mutate 16S rrnB operator.
2. Mutated RBS of RFP and checked through gel electrophoresis.
July 14th, 2012
- Transform two plasmids of we got yestday together into E.coli.
- PCR verification of colonies on the LB plates.
- Inculcated the right colonies in Liquid LB.
