Difference between revisions of "Part:BBa K533002:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | Compared to part [[Part:BBa_K533001 | BBa_K533001]], we inserted an HIV-protease site between OmpA and SH3 to allow a proteolytic release of the cargo. | ||
+ | This device is also under the drive of T7 promoter and lac repressor, allowing for strong inducible expression with IPTG in BL21 E. coli strain. | ||
===Source=== | ===Source=== |
Latest revision as of 15:03, 5 October 2011
OmpA-HIV protease site-SH3
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 857
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Compared to part BBa_K533001, we inserted an HIV-protease site between OmpA and SH3 to allow a proteolytic release of the cargo.
This device is also under the drive of T7 promoter and lac repressor, allowing for strong inducible expression with IPTG in BL21 E. coli strain.
Source
OmpA is from BL21(DE3) E. Coli genomic DNA. SH3 is from human Grb2 protein. HIV protease site is from a former part.