Difference between revisions of "Part:BBa K5422011:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | During the design of this sequence, we optimized the codons for efficient expression in | + | During the design of this sequence, we optimized the codons for efficient expression in E. coli and ensured compatibility with BioBrick and Type IIS assembly standards. Additionally, we made adjustments to prevent secondary structures that could affect transcription and translation efficiency, and to facilitate the synthesis process by IDT. Importantly, these modifications involved synonymous codon changes, ensuring no alteration in the amino acid sequence. |
Latest revision as of 12:14, 30 September 2024
Dual Protein Expression System
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 709
Design Notes
During the design of this sequence, we optimized the codons for efficient expression in E. coli and ensured compatibility with BioBrick and Type IIS assembly standards. Additionally, we made adjustments to prevent secondary structures that could affect transcription and translation efficiency, and to facilitate the synthesis process by IDT. Importantly, these modifications involved synonymous codon changes, ensuring no alteration in the amino acid sequence.
Source
The DNA sequence for this part was synthesized by Integrated DNA Technologies (IDT) based on a custom design tailored for our project specifications.