Difference between revisions of "Part:BBa K3110041"
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lldRO1 and lldRO2 are the operator regions which bind to the regulator element lldR and inhibit transcription. Upon binding of L-Lactate to lldR, however, this transcriptional suppression is lost and instead lldR complex with L-Lactate remains bound to lldRO1 acting as a transcriptional activator. By using RBS of different strengths we are trying to find out the optimum construct which will give output (in our case the output is super-folded GFP or sfGFP) that can efficiently discriminate cancer vs non-cancer microenvironments. | lldRO1 and lldRO2 are the operator regions which bind to the regulator element lldR and inhibit transcription. Upon binding of L-Lactate to lldR, however, this transcriptional suppression is lost and instead lldR complex with L-Lactate remains bound to lldRO1 acting as a transcriptional activator. By using RBS of different strengths we are trying to find out the optimum construct which will give output (in our case the output is super-folded GFP or sfGFP) that can efficiently discriminate cancer vs non-cancer microenvironments. | ||
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<partinfo>BBa_K3110041 parameters</partinfo> | <partinfo>BBa_K3110041 parameters</partinfo> | ||
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+ | <h1>Characterization </h1> | ||
+ | Due to shortage of time we could not characterize this construct. |
Latest revision as of 15:55, 21 October 2019
lldRO1-J23117-lldRO2 Medium RBS sfGFP
lldRO1 and lldRO2 are the operator regions which bind to the regulator element lldR and inhibit transcription. Upon binding of L-Lactate to lldR, however, this transcriptional suppression is lost and instead lldR complex with L-Lactate remains bound to lldRO1 acting as a transcriptional activator. By using RBS of different strengths we are trying to find out the optimum construct which will give output (in our case the output is super-folded GFP or sfGFP) that can efficiently discriminate cancer vs non-cancer microenvironments.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 78
Illegal NheI site found at 101 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 175
Characterization
Due to shortage of time we could not characterize this construct.