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Team:Paris/Parts/Plastest
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= Plasmid for promoter Amplification & Measurement = | = Plasmid for promoter Amplification & Measurement = | ||
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One derivated plasmid do not have the RBS B0032 outside the BioBrick site, it allows to test the influence of the RBS in changing it in the BioBrick. To do so, [[team:Paris/Notebook/Oligo|O142]] does not contains the RBS, the PCR will begin directly at the ATG codon. | One derivated plasmid do not have the RBS B0032 outside the BioBrick site, it allows to test the influence of the RBS in changing it in the BioBrick. To do so, [[team:Paris/Notebook/Oligo|O142]] does not contains the RBS, the PCR will begin directly at the ATG codon. | ||
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== Oligonucleotides design == | == Oligonucleotides design == | ||
Latest revision as of 06:50, 30 October 2008
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Plasmid for promoter Amplification & Measurement
Those plasmids are very useful vectors to amplify promoters and to measure their forces using Standard Promoter Units. The principle is easy to understand. The plasmid contains the BioBrick restriction sites (EcoRI, XbaI, SpeI and PstI) followed by the standard GFP Tripart (E0240). Instead of using a big biobrick containing Promoter, RBS, GFP and Terminators, the Biobrick used for the test is only the Promoter. This plasmid can be used to amplify a promoter because only the promoter is in the biobrick.
One derivated plasmid do not have the RBS B0032 outside the BioBrick site, it allows to test the influence of the RBS in changing it in the BioBrick. To do so, O142 does not contains the RBS, the PCR will begin directly at the ATG codon.
Oligonucleotides design
Creation of 3 oligonucleotides (O140, O141, O142) in order to create two particular plasmids.
Construction of the Plasmid
Necessary material
- Oligos O140, O141 and O142
- E0240
- pSB3K3
