Difference between revisions of "Part:BBa K733002:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | In the xylR region, there are three illegal cutting sites – one EcoRI cutting site and two XbaI cutting sites. We first check with the codon usage in B. subtilis and design a sequence for xylR without these illegal cutting sites. Then, we used PCR mutagenesis to eliminate these three illegal cutting sites. | ||
===Source=== | ===Source=== |
Revision as of 16:43, 22 September 2012
xylR+PxylA: A xylose inducible promoter with its transcriptional regulator.
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 847
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
In the xylR region, there are three illegal cutting sites – one EcoRI cutting site and two XbaI cutting sites. We first check with the codon usage in B. subtilis and design a sequence for xylR without these illegal cutting sites. Then, we used PCR mutagenesis to eliminate these three illegal cutting sites.
Source
Not available at this moment.