Difference between revisions of "Part:BBa K5366025:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | We ensured that the forward and reverse primer had 20 bp of homology to the plasmid.We needed to purify the HDM protein, so we attached the 6×His tag after HDM. | |
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===Source=== | ===Source=== |
Revision as of 15:49, 27 September 2024
T7 promoter-RBS-HDM-6xHis -T7 termonator
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1555
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 402
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We ensured that the forward and reverse primer had 20 bp of homology to the plasmid.We needed to purify the HDM protein, so we attached the 6×His tag after HDM.
Source
Thermotogales bacterium