Difference between revisions of "Part:BBa K4477006:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | We aimed for 75% relative expression so as to | + | We used a pre-existing RBS, BBa_J61100, as a starting point for Salis optimization. We aimed for 75% relative expression so as to achieve a high level of protein expression of BBa_K4477001 without overburdening the <em>E. coli</em> expressing the gene. |
− | + | ||
+ | We adjusted the RBS sequence to remove restriction sites that would make the RBS incompatible with various assembly methods. | ||
===Source=== | ===Source=== |
Latest revision as of 08:35, 12 October 2022
RBS for expression of human/mouse anti-apoB(MDA) antibody light chain
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
We used a pre-existing RBS, BBa_J61100, as a starting point for Salis optimization. We aimed for 75% relative expression so as to achieve a high level of protein expression of BBa_K4477001 without overburdening the E. coli expressing the gene.
We adjusted the RBS sequence to remove restriction sites that would make the RBS incompatible with various assembly methods.
Source
https://salislab.net/software/