Difference between revisions of "Part:BBa K1893006:Design"
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===Source=== | ===Source=== | ||
− | The CinR part was synthesised and assembled using Biobrick assembly with the other components. | + | The CinR part was synthesised by GeneArt by Thermofisher and assembled using Biobrick assembly with the other components. |
===References=== | ===References=== |
Latest revision as of 11:13, 23 October 2016
Cin receiver (CinR+pCin)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 611
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part does not include an LVA tag on the CinR gene. This means that the protein is not rapidly degraded. When active, the CinR protein binds to the pCin promoter, activating transcription of downstream genes. This part contains everything necessary for O3C14-HSL-induced expression of genes inserted downstream of the pCin promoter.
Source
The CinR part was synthesised by GeneArt by Thermofisher and assembled using Biobrick assembly with the other components.