Difference between revisions of "Part:BBa K515107:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
<html> | <html> | ||
− | <p>The original Dendra2 sequence had been joint codon optimized for <i>Escherichia coli</i> and <i>Bacillus subtilis<i> and designed to contain the insulator sequence under the influence of a strong RBS. However it could not be synthesised. We therefore allowed Eurofins to codon optimize it for <i>E. coli</i> and only had the coding region synthesised with a prefix and a suffix. Once the gene arrived, we assembled it using standard BioBrick assembly with the TetR repressible promoter <a href="https://parts.igem.org/Part:BBa_R0040"/>(BBa_R0040)</a> and a standard RBS <a href="https://parts.igem.org/Part:BBa_R0034"/>(BBa_R0034)</a>. | + | <p>The original Dendra2 sequence had been joint codon optimized for <i>Escherichia coli</i> and <i>Bacillus subtilis</i> and designed to contain the insulator sequence under the influence of a strong RBS. However it could not be synthesised. We therefore allowed Eurofins to codon optimize it for <i>E. coli</i> and only had the coding region synthesised with a prefix and a suffix. Once the gene arrived, we assembled it using standard BioBrick assembly with the TetR repressible promoter <a href="https://parts.igem.org/Part:BBa_R0040"/>(BBa_R0040)</a> and a standard RBS <a href="https://parts.igem.org/Part:BBa_R0034"/>(BBa_R0034)</a>. |
</html> | </html> |
Latest revision as of 14:37, 21 September 2011
Composite p(tetR) - Dendra2
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
The original Dendra2 sequence had been joint codon optimized for Escherichia coli and Bacillus subtilis and designed to contain the insulator sequence under the influence of a strong RBS. However it could not be synthesised. We therefore allowed Eurofins to codon optimize it for E. coli and only had the coding region synthesised with a prefix and a suffix. Once the gene arrived, we assembled it using standard BioBrick assembly with the TetR repressible promoter (BBa_R0040) and a standard RBS (BBa_R0034).
Source
-