Difference between revisions of "Part:BBa K1065302:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This part has been created first by inserting the RBS sequence between pFixK2 and amilGFP (in Bba_K952003) through mutagenesis PCR with a specific primer | + | This part has been created first by inserting the RBS sequence between pFixK2 and amilGFP (in Bba_K952003) through mutagenesis PCR with a specific primer. <br>Furthermore we decided to regulate transcription with an upstream promoter, pLac (BBa_R0010). |
===Source=== | ===Source=== |
Revision as of 20:19, 23 September 2013
Blue light sensing device without inverter for the production of amilGFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 770
Illegal NgoMIV site found at 842
Illegal NgoMIV site found at 932
Illegal NgoMIV site found at 950
Illegal NgoMIV site found at 1462
Illegal NgoMIV site found at 1755
Illegal NgoMIV site found at 1849
Illegal AgeI site found at 484
Illegal AgeI site found at 1630 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1519
Illegal BsaI.rc site found at 383
Design Notes
This part has been created first by inserting the RBS sequence between pFixK2 and amilGFP (in Bba_K952003) through mutagenesis PCR with a specific primer.
Furthermore we decided to regulate transcription with an upstream promoter, pLac (BBa_R0010).
Source
The part come from a BioBrick already present in the registry