![](https://parts.igem.org/images/partbypart/icon_rbs.png)
RBS
Part:BBa_J100467:Design
Designed by: Julia Pharr Group: Campbell M Lab (2018-11-08)
A new RBS in E. coli to code for mScarlet protein
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
Watson-Crick and Non-Watson-Crick base pairing was predominantly considered in the development of the new RBS. Our group had to determine the most effective combination of both kinds of base pairing in order to ensure the new RBS had a high affinity for the ribosomal RNA.
Source
Our group designed the new RBS ourselves, largely base on the research in the paper written by Dr. Campbell because of the evidence there that suggested that Non-Watson-Crick base pairing was advantageous in creating a new RBS in E. coli.