Team:RMIT Australia/Project
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=== Making the Inducible T7 Expression Vector === | === Making the Inducible T7 Expression Vector === | ||
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+ | The aim for this section is to create a an inducible expression backbone. this will be achieved by altering the backbone biobrick '''BBa_J04500''', by removing the -35 and -10 elements (promoter) and inserting the bacteriophage T7 promoter. the strategy used to will be Quikchange XL mutagenesis to alter the promoter elements into restriction sites: | ||
+ | * -35 --> AflII | ||
+ | * -10 --> BamH1 | ||
+ | |||
+ | These restriction sites are NOT found in the BBa_J04500 part or vector (pSB1A2), so there will be no cross cutting. | ||
== Results == | == Results == |
Revision as of 21:14, 6 July 2010
Overall project
Your abstract
Project Details
Creation of the Taq Polymerase Part
Making the Inducible T7 Expression Vector
The aim for this section is to create a an inducible expression backbone. this will be achieved by altering the backbone biobrick BBa_J04500, by removing the -35 and -10 elements (promoter) and inserting the bacteriophage T7 promoter. the strategy used to will be Quikchange XL mutagenesis to alter the promoter elements into restriction sites:
- -35 --> AflII
- -10 --> BamH1
These restriction sites are NOT found in the BBa_J04500 part or vector (pSB1A2), so there will be no cross cutting.