Measurement
Part:BBa_J100432:Design
Designed by: Tatianna Travieso Group: Campbell M Lab (2018-06-28)
T7 Consensus Promoter in pClone mScarlet
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 895
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 895
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 895
Illegal BamHI site found at 841 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 895
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 895
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The paper referenced earlier discussed studies that found an "initiation domain" and a "binding domain" from -12 to +5, both of which were essential for successful transcription and translation.
Source
"T7 promoter essential for promoter activity in vivo" by Richard A. Ikeda et al. (1992), https://www.ncbi.nlm.nih.gov/pubmed/1598210 Consensus sequence, https://parts.igem.org/Promoters/Catalog/T7Promoters/Catalog/T7