Difference between revisions of "Part:BBa K1075011:Design"
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− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1075011 short</partinfo> | <partinfo>BBa_K1075011 short</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
− | We used the same amino acid sequence as used for the light inducible heterodimerisation system from Lungu et al. | + | We used the same amino acid sequence as used for the light inducible heterodimerisation system from Lungu et al. (2012). |
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===Source=== | ===Source=== | ||
− | It was PCR amplified from a plasmid containing full length Vinculin from M. musculus. | + | It was PCR amplified from a plasmid containing full length Vinculin from ''M. musculus''. |
===References=== | ===References=== | ||
+ | [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334866/]Lungu et al. (2012) Designing photoswitchable peptides using the AsLOV2 domain |
Revision as of 09:51, 4 October 2013
Vinculin D1
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 56
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We used the same amino acid sequence as used for the light inducible heterodimerisation system from Lungu et al. (2012).
Source
It was PCR amplified from a plasmid containing full length Vinculin from M. musculus.
References
[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334866/]Lungu et al. (2012) Designing photoswitchable peptides using the AsLOV2 domain