Difference between revisions of "Part:BBa R0051"
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The cI regulated promoter is based on the pR promoter from bacteriophage lambda. The promoter has two DNA binding sites for lambda cI repressor <bbpart>BBa_C0051</bbpart>. cI binding results in repression of transcription. The specific sequence used here is based on the cI repressible promoter used in the Elowitz repressilator (and references therein). | The cI regulated promoter is based on the pR promoter from bacteriophage lambda. The promoter has two DNA binding sites for lambda cI repressor <bbpart>BBa_C0051</bbpart>. cI binding results in repression of transcription. The specific sequence used here is based on the cI repressible promoter used in the Elowitz repressilator (and references therein). | ||
| − | [google.com] | + | [google.com f] |
Intrinsic noise value: 0.0869 (compare with R0010: 0.0707; R0011: 0.0040). See [http://2015.igem.org/Team:William_and_Mary William_and_Mary iGEM 2015] | Intrinsic noise value: 0.0869 (compare with R0010: 0.0707; R0011: 0.0040). See [http://2015.igem.org/Team:William_and_Mary William_and_Mary iGEM 2015] | ||
Revision as of 21:27, 13 October 2018
promoter (lambda cI regulated)
The cI regulated promoter is based on the pR promoter from bacteriophage lambda. The promoter has two DNA binding sites for lambda cI repressor BBa_C0051. cI binding results in repression of transcription. The specific sequence used here is based on the cI repressible promoter used in the Elowitz repressilator (and references therein). [google.com f] Intrinsic noise value: 0.0869 (compare with R0010: 0.0707; R0011: 0.0040). See [http://2015.igem.org/Team:William_and_Mary William_and_Mary iGEM 2015]
Usage and Biology
Strong promoter. [jb, 5/24/04]
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]