Difference between revisions of "Part:BBa K4477003:Design"
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===Source=== | ===Source=== | ||
− | Amino acid sequences for IK17 light and heavy chains acquired from NCBI: | + | Amino acid sequences for IK17 light and heavy chains acquired from NCBI: <br> |
− | heavy: https://www.ncbi.nlm.nih.gov/protein/AAK93956.1 | + | heavy: https://www.ncbi.nlm.nih.gov/protein/AAK93956.1 <br> |
light: https://www.ncbi.nlm.nih.gov/protein/AAK93957.1 | light: https://www.ncbi.nlm.nih.gov/protein/AAK93957.1 | ||
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===References=== | ===References=== | ||
1. https://www.jacc.org/doi/full/10.1016/j.jacc.2011.07.017 <br> | 1. https://www.jacc.org/doi/full/10.1016/j.jacc.2011.07.017 <br> | ||
2. https://pubmed.ncbi.nlm.nih.gov/14644097/ | 2. https://pubmed.ncbi.nlm.nih.gov/14644097/ |
Revision as of 08:15, 12 October 2022
IK17 (anti-oxLDL) scFv antibody fragment
- 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 486
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Amino acid sequence reverse transcribed and codon optimized for expression in E. coli B (the parent strain of SHuffle).
His tag and TEV cleavage sites were included downstream of the start codon but upstream of the antibody coding sequence. The His tag ensured the entire polypeptide could be purified out of a total protein solution using immobilized metal ion affinity chromatography (IMAC), and the TEV cleavage site ensured that TEV could be used to cleave off the His tag once it was no longer needed.
For detailed annotations, see Team Virginia 2022's Benchling folder here: https://benchling.com/mrkhoury/f_/YR4zZSUb-virginia-igem-2022-dna-constructs/
Source
Amino acid sequences for IK17 light and heavy chains acquired from NCBI:
heavy: https://www.ncbi.nlm.nih.gov/protein/AAK93956.1
light: https://www.ncbi.nlm.nih.gov/protein/AAK93957.1
References
1. https://www.jacc.org/doi/full/10.1016/j.jacc.2011.07.017
2. https://pubmed.ncbi.nlm.nih.gov/14644097/