Device
Part:BBa_K1791004:Design
Designed by: Graeme Glaister Group: iGEM15_Lethbridge (2015-09-23)
T7 promoter fused with a theophylline inducible ribozyme (aptazyme)
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
by changing the T7 promoter sequence (BBa_I719005) slightly after the GGG trinulceotide we get an increase in the potential for generating RNA with our composite parts BBa_K1791001 and BBa_K1791002.
Source
Win, M.N., Smolke C.D. 2007 and BBa_I719005