Difference between revisions of "Part:BBa K1017401:Design"
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===Design Notes=== | ===Design Notes=== | ||
Included the sRNA-1 we designed and its complement DNA sequence to produce RBS binding site. | Included the sRNA-1 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=== | ===Source=== | ||
Latest revision as of 12:13, 22 September 2013
sRNA+rRBS-1
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 144
Illegal SpeI site found at 129 - 12INCOMPATIBLE WITH RFC[12]Illegal SpeI site found at 129
Illegal NotI site found at 135 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 147
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 144
Illegal SpeI site found at 129 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 144
Illegal SpeI site found at 129 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
Included the sRNA-1 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
sythesis