Difference between revisions of "Part:BBa K4604015:Design"
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===Source=== | ===Source=== | ||
− | Modified piG_01a using Gibson Assembly. | + | Modified piG_01a (BBa_K4604016) using Gibson Assembly. |
===References=== | ===References=== |
Revision as of 15:54, 7 October 2023
piG_01b (tetR_bluB)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 710
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1618
Design Notes
The start codon of the bluB was changed to ATG to act as a start for translation in E. coli. The region downstream of the tetA/R promoter was shortened (in comparison to piG_01a/BBa_K4604016) to counteract the leakiness.
Source
Modified piG_01a (BBa_K4604016) using Gibson Assembly.