Difference between revisions of "Part:BBa J100071:Design"
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===Design Notes=== | ===Design Notes=== | ||
We cloned the promoter region 334 bp upstream of the transcription start site, in which Cad1 and Cad2 are included. | We cloned the promoter region 334 bp upstream of the transcription start site, in which Cad1 and Cad2 are included. | ||
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===Source=== | ===Source=== | ||
Latest revision as of 14:39, 5 July 2012
cadA promoter
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 cloned the promoter region 334 bp upstream of the transcription start site, in which Cad1 and Cad2 are included.
Source
Taken from E. coli genome through PCR.