Difference between revisions of "Part:BBa K1980006:Design"
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<partinfo>BBa_K1980006 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1980006 SequenceAndFeatures</partinfo> | ||
+ | Designed so that any protein can be ligated to this part with standard assembly to make them respond to copper (for instance our copper chelator proteins) | ||
===Design Notes=== | ===Design Notes=== | ||
− | Codon optimised. Designed for biobrick assembly with reporter of choice | + | Codon optimised. Designed for biobrick assembly with protein/reporter of choice. |
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===Source=== | ===Source=== | ||
− | E. coli | + | <i>E. coli</i>. Ordered as codon optimised DNA from IDT. |
===References=== | ===References=== |
Revision as of 20:57, 12 October 2016
pCopA with divergent expressed CueR
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 438
Illegal NheI site found at 461 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Designed so that any protein can be ligated to this part with standard assembly to make them respond to copper (for instance our copper chelator proteins)
Design Notes
Codon optimised. Designed for biobrick assembly with protein/reporter of choice.
Source
E. coli. Ordered as codon optimised DNA from IDT.