Difference between revisions of "Part:BBa K165095"
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[[Image:Glyph_labeled2.png|center|400px]] | [[Image:Glyph_labeled2.png|center|400px]] | ||
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+ | To build a functional limiter, this part should be in a yeast strain with the following constructs: | ||
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+ | A: [[Part:BBa_K165080]] pGAL1 + Untagged LexA activator on pRS305 | ||
+ | G: | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 05:16, 30 October 2008
Gli1 bs + LexA bs + mCYC + Zif268-HIV repressor (mCherryx2 tagged) on pRS303
This devise constitutes the alpha element in one instance of our limiter construct. It is placed in a mutually inhibitory relationship with the tau element. Under the control of the same promoter as the gene of interest, alpha serves as a readout of its level of induction. In a superthreshold state, it represses tau, allowing R to be expressed and repress G back the threshold level.
To build a functional limiter, this part should be in a yeast strain with the following constructs:
A: Part:BBa_K165080 pGAL1 + Untagged LexA activator on pRS305 G:
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 534
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 534
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2321
Illegal XhoI site found at 1
Illegal XhoI site found at 122
Illegal XhoI site found at 284 - 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 534
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 534
Illegal AgeI site found at 3464 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 119
Illegal SapI.rc site found at 1492
Illegal SapI.rc site found at 2085