Difference between revisions of "Part:BBa K4604018:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | Site directed mutagenesis was done between the tet promoter and RBS to remove a EcoRI restriction site. | + | Site directed mutagenesis was done between the tet promoter and RBS to remove a EcoRI restriction site. The region downstream of the tetA/R promoter was shortened (in comparison to piG_01a/BBa_K4604016) to counteract the leakiness. |
Revision as of 15:54, 7 October 2023
piG_02b (tetR_riboK12_mazF_mTurq)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 710
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 883
Illegal AgeI site found at 1376 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2250
Design Notes
Site directed mutagenesis was done between the tet promoter and RBS to remove a EcoRI restriction site. The region downstream of the tetA/R promoter was shortened (in comparison to piG_01a/BBa_K4604016) to counteract the leakiness.
Source
Modified piG_02a (BBBa_K4604017) using Gibson Assembly.