Composite
Part:BBa_K781006:Design
Designed by: Kevin Chen Group: iGEM12_Queens_Canada (2012-10-03)
[R0010][B0034] - RFP-FliC Deletion Chimera
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1884
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 529
Illegal AgeI site found at 1362
Illegal AgeI site found at 1474 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
The linker and D3 overlap sequences are standard for our parts. By digesting the plasmid with the two inner enzymes, SpeI and NheI for our BB-2 standard parts, you can purify and then PCR overlap extend using the following protocol to result in a brand new chimera. Note that there are two different formats for making flagellin insertion variants and deletion variants
Source
This part was PCR amplified from J04450 and then overlap extension was used to incorporate it into the plasmid.