Device
Part:BBa_J100272:Experience
Designed by: Malcolm Campbell Group: Campbell M Lab (2016-06-21)
The problem with rClone Red v1 [J119384] was that the RBS we used was complementary to an "anti-RBS" located in RFP.
To fix this problem, we mutated three codons so that they encoded the same 3 amino acids, but the resulting mRNA would not form the hairpin loop because we had disrupted the anti-RBS (Eckdahl et al., 2017).
By removing the anti-RBS, the same RBS sequence now worked 10 times better than it had in rClone Red v1.
We recommend everyone use J100272, rClone Red v2 as the preferred plasmid.
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