Difference between revisions of "Part:BBa K1017402:Design"
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===Design Notes=== | ===Design Notes=== | ||
Included the sRNA-2 we designed and its complement DNA sequence to produce RBS binding site. | Included the sRNA-2 we designed and its complement DNA sequence to produce RBS binding site. | ||
− | + | We can use this two complement parts to control on or off of other operons. | |
Latest revision as of 12:35, 22 September 2013
sRNA+rRBS-2
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 97
Illegal SpeI site found at 82 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 82
Illegal NotI site found at 88 - 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 3
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 97
Illegal SpeI site found at 82 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 97
Illegal SpeI site found at 82 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Included the sRNA-2 we designed and its complement DNA sequence to produce RBS binding site. We can use this two complement parts to control on or off of other operons.
Source
synthesis