Reporter
Part:BBa_K1758101:Design
Designed by: Team Bielefeld-CeBiTec 2015 Group: iGEM15_Bielefeld-CeBiTec (2015-08-17)
Translation enhancing 5-UTR + sfGFP
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 59
Design Notes
[http://www.ncbi.nlm.nih.gov/pubmed/23654270 Lentini et al. 2013] showed that the scar which is created by standard biobrick assembly is disadvantageous for in vitro translation when occuring between RBS and start codon. Therefore we changed the sequence between RBS and start codon for other parts.
Source
This part was created by shortening BBa_I746909 and simultaneously adding 5'-UTR via Gibson primers.
Amplification with Gibson-primers: