Difference between revisions of "Part:BBa K4477012:Design"
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Amino acid sequences were reverse transcribed and codon optimized for expression in E. coli B (the parent strain of SHuffle). In addition, further codon optimization was used to remove illegal restriction sites from the construct. | Amino acid sequences were reverse transcribed and codon optimized for expression in E. coli B (the parent strain of SHuffle). In addition, further codon optimization was used to remove illegal restriction sites from the construct. | ||
| − | A two-way terminator was used so that | + | A two-way terminator was used so that any genes in the vector in which this insert will be inserted that happen to be on the strand opposite to the strand encoding the insert will not be read backward into the insert and interfere with transcription of our antibody of interest. |
===Source=== | ===Source=== | ||
Revision as of 13:15, 12 October 2022
IK17 (anti-oxLDL) scFv - complete expression cassette
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 576
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Amino acid sequences were reverse transcribed and codon optimized for expression in E. coli B (the parent strain of SHuffle). In addition, further codon optimization was used to remove illegal restriction sites from the construct.
A two-way terminator was used so that any genes in the vector in which this insert will be inserted that happen to be on the strand opposite to the strand encoding the insert will not be read backward into the insert and interfere with transcription of our antibody of interest.
Source
1. https://www.jacc.org/doi/full/10.1016/j.jacc.2011.07.017
2. https://pubmed.ncbi.nlm.nih.gov/14644097/