Difference between revisions of "Part:BBa K900001:Design"
(→Source) |
|||
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
Codon optimization for yeast and internal restriction site removal to be compatible with our Golden Gate cloning scheme. | Codon optimization for yeast and internal restriction site removal to be compatible with our Golden Gate cloning scheme. | ||
− | |||
− | |||
===Source=== | ===Source=== |
Revision as of 01:40, 4 October 2012
PAGFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Codon optimization for yeast and internal restriction site removal to be compatible with our Golden Gate cloning scheme.
Source
Synthesized in house and cloned into Addgene plasmid [http://www.addgene.org/11911/ l11911] Previously engineered version of RFP from Patterson and Lippincott-Schwartz, 2002.
References
Patterson, G. H. & Lippincott-Schwartz, J. A Photoactivatable GFP for Selective Photolabeling of Proteins and Cells. Science 297, 1873–1877 (2002).