Difference between revisions of "Part:BBa K5226031:Design"
(→Design Notes) |
(→Design Notes) |
||
Line 7: | Line 7: | ||
===Design Notes=== | ===Design Notes=== | ||
− | Although this part complies with one of the RFC 10 or Type IIS standards, it is inconsistent with the standards upheld by other basic parts. As a result, the composite component formed by their combination has illegal sites, necessitating a synonymous mutation. Mutate the base pairs at 48bp of | + | Although this part complies with one of the RFC 10 or Type IIS standards, it is inconsistent with the standards upheld by other basic parts. As a result, the composite component formed by their combination has illegal sites, necessitating a synonymous mutation. Mutate the base pairs at 48bp of hbD from a/t to g/c. |
===Source=== | ===Source=== |
Latest revision as of 01:36, 2 October 2024
4hbD
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
Although this part complies with one of the RFC 10 or Type IIS standards, it is inconsistent with the standards upheld by other basic parts. As a result, the composite component formed by their combination has illegal sites, necessitating a synonymous mutation. Mutate the base pairs at 48bp of hbD from a/t to g/c.
Source
PCR amplification.Sequence source is from Clostridium kluyveri DSM 555, found through NCBI (https://www.ncbi.nlm.nih.gov/nucleotide/CP000673.1?report=genbank&log$=nuclalign&blast_rank=2&RID=D0800NU9013&from=3061070&to=3062185)