Team:Panama/20 July 2010
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Activities: | Activities: | ||
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+ | '''Methodology Steps:''' | ||
1.Locate the BioBrick parts that we are going to assemble, in the distribution plates. | 1.Locate the BioBrick parts that we are going to assemble, in the distribution plates. | ||
RBS: 2M, GFP: 14K, Terminator: 13D & Promoter: 15N | RBS: 2M, GFP: 14K, Terminator: 13D & Promoter: 15N | ||
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For that we take the DNA from each of the wells of the plate. We then have to take 2ul of each one and put it in the bacteria. The other 8ul we are to store at -20°C | For that we take the DNA from each of the wells of the plate. We then have to take 2ul of each one and put it in the bacteria. The other 8ul we are to store at -20°C |
Revision as of 20:28, 15 October 2010
July 20
Activities:
Methodology Steps:
1.Locate the BioBrick parts that we are going to assemble, in the distribution plates.
RBS: 2M, GFP: 14K, Terminator: 13D & Promoter: 15N
For that we take the DNA from each of the wells of the plate. We then have to take 2ul of each one and put it in the bacteria. The other 8ul we are to store at -20°C
2.Clone the chosen BioBrick parts in competent E. coli.
For the extraction we follow the comercial protocol.
We transformed 4 different bacteria, for the different BioBrick plasmids & prepared LB-ampi.
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