Difference between revisions of "Part:BBa K4432122:Design"
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===Source=== | ===Source=== | ||
− | DNA synthesis & Assembly | + | DNA synthesis, PCR amplification & Assembly |
===References=== | ===References=== |
Latest revision as of 21:14, 26 September 2022
idi and dsx expression operon under the control of the T5 promoter
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 500
- 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 500
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 674
Illegal BamHI site found at 681 - 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 500
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 500
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1435
Design Notes
T5 promoter (BBa_K4432000) + custom made RBS (BBa_K4432012) + idi coding sequence (BBa_K3166068) + custom made RBS (BBa_K4432013) + dxs coding sequence (BBa_K3166061)
Source
DNA synthesis, PCR amplification & Assembly