Difference between revisions of "Part:BBa K4387990:Design"
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | The amino acid sequence was converted into DNA | + | The amino acid sequence was converted into DNA and then codon optimized for E. coli with the help of the codon optimization tool provided by Integrated DNA Technologies (IDT). The same linker was used as the one described in the patent. [1] |
− | + | ||
===Source=== | ===Source=== | ||
+ | The amino acid sequence was directly taken from the patent mentioned in the description. [1] | ||
− | |||
===References=== | ===References=== | ||
+ | * [1] Silence, Karen, Lauwereys, Marc, De Haard, Hans, et al. "Single domain antibodies directed against tumour necrosis factor-alpha and uses therefor", Int. Publication Number: WO 2004/041862 A2, 21 May 2004 |
Latest revision as of 15:52, 8 October 2022
Bivalent Anti-Tumour Necrosis Factor Nanobody (VHH#3E + VHH#2B)
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
The amino acid sequence was converted into DNA and then codon optimized for E. coli with the help of the codon optimization tool provided by Integrated DNA Technologies (IDT). The same linker was used as the one described in the patent. [1]
Source
The amino acid sequence was directly taken from the patent mentioned in the description. [1]
References
- [1] Silence, Karen, Lauwereys, Marc, De Haard, Hans, et al. "Single domain antibodies directed against tumour necrosis factor-alpha and uses therefor", Int. Publication Number: WO 2004/041862 A2, 21 May 2004