Difference between revisions of "Part:BBa K318500:Design"
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===Source=== | ===Source=== | ||
| − | The RcsA gene we used was originally submitted by CalTech 2008 | + | The RcsA gene we used was originally submitted by CalTech 2008 BBa_K137113. |
===References=== | ===References=== | ||
Latest revision as of 23:09, 26 October 2010
lacI pL + RBS + RcsA + TT
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We wanted to test what IPTG induction levels were appropiate to protect our cells from an acidic environment of pH=2 before placing our devices under constitute control with appropriate RBS's.
Source
The RcsA gene we used was originally submitted by CalTech 2008 BBa_K137113.