Difference between revisions of "Part:BBa K133055:Design"
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===Source=== | ===Source=== | ||
| − | + | Red Flourescence Protein was obtaind from previousely designed biobrick of 2007 iGEM team Ljubljana containing Red Flourescence Protein with added nuclear localisation signal and mutated PstI restriction site. | |
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===References=== | ===References=== | ||
Latest revision as of 01:01, 30 October 2008
mCherry
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 686
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The part was cloned into pSB1.AK3 without terminator for use in bacterial cells (surface expression).
Source
Red Flourescence Protein was obtaind from previousely designed biobrick of 2007 iGEM team Ljubljana containing Red Flourescence Protein with added nuclear localisation signal and mutated PstI restriction site.