Difference between revisions of "Part:BBa K1141002:Design"
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__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1141002 short</partinfo> | <partinfo>BBa_K1141002 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
− | + | In the original sequence coming from the pQE30 plasmid (see part BBa_K1141001) there was an Ecor1 restriction site between the promoter and the RBS. We removed this site in order to made this biobrick compatible with RFC[10], and 3A assembly. | |
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===Source=== | ===Source=== | ||
− | KillerRed came from | + | The KillerRed coding sequence originally came from the ADDGENE plasmid pBabe-KR-CENPA |
===References=== | ===References=== |
Revision as of 21:20, 1 October 2013
Plac-RBS-KillerRed (IPTG-inducible)
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 133
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 289
Illegal BsaI.rc site found at 580
Design Notes
In the original sequence coming from the pQE30 plasmid (see part BBa_K1141001) there was an Ecor1 restriction site between the promoter and the RBS. We removed this site in order to made this biobrick compatible with RFC[10], and 3A assembly.
Source
The KillerRed coding sequence originally came from the ADDGENE plasmid pBabe-KR-CENPA