Difference between revisions of "Part:BBa K524001:Design"
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===Design Notes=== | ===Design Notes=== | ||
| − | A stop codon was added to the end of the CDS to terminate translation of sfGFP1-10 | + | A stop codon was added to the end of the CDS to terminate translation of sfGFP1-10. |
| − | + | RBS was introduced into primers for cloning. | |
| − | + | ||
===Source=== | ===Source=== | ||
Revision as of 19:10, 3 October 2011
pLac + RBS + split sfGFP 1-10
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 238
Design Notes
A stop codon was added to the end of the CDS to terminate translation of sfGFP1-10. RBS was introduced into primers for cloning.
Source
Constructed from 2011 iGEM DNA Repository Plates and Boxes, Spring Distribution, BBa_I746908
References
Stéphanie Cabantous, Thomas C Terwilliger & Geoffrey S Waldo.(2004).Protein tagging and detection with engineered self-assembling fragments of green fluorescent protein.Nature Biotechnology 23, 102 - 107