Difference between revisions of "Part:BBa K4676000:Design"
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===Source=== | ===Source=== | ||
− | This sequence was created by truncating the much larger h-fibroin sequence, which was published as supplementary information by Heckenhauer et al. for their paper "Characterization of the primary structure of the major silk gene, h-fibroin, across caddisfly (Trichoptera) suborders." | + | This sequence was created by truncating the much larger h-fibroin sequence, which was published as supplementary information by Heckenhauer et al. for their paper "Characterization of the primary structure of the major silk gene, h-fibroin, across caddisfly (Trichoptera) suborders." (1) |
===References=== | ===References=== |
Revision as of 21:04, 11 October 2023
Truncated Control H-Fibroin of G. Pellucidus
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
There are different versions of the RM1 and RM2 motiffs in the h-fibroin gene. When creating this part, only the first RM1 version that shows up in the gene was included, and only the first RM2 version that shows up in the gene was included. Furthermore, this sequence has been codon optimized using the biotechnology platform Benchling.
Source
This sequence was created by truncating the much larger h-fibroin sequence, which was published as supplementary information by Heckenhauer et al. for their paper "Characterization of the primary structure of the major silk gene, h-fibroin, across caddisfly (Trichoptera) suborders." (1)