Difference between revisions of "Part:BBa K5226033:Design"
(→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 30bp of ogdA from a/t to g/c.Mutate the base pairs at 30bp of ogdA from a/t to c/g. | |
− | + | ||
− | + | ||
===Source=== | ===Source=== |
Latest revision as of 01:44, 2 October 2024
ogdA
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 30bp of ogdA from a/t to g/c.Mutate the base pairs at 30bp of ogdA from a/t to c/g.
Source
PCR amplification.Sequence source is from Synechococcus sp. PCC 7002, found through NCBI(https://www.ncbi.nlm.nih.gov/nucleotide/CP000951.1?report=genbank&log$=nuclalign&blast_rank=1&RID=CZS2C9VF013&from=2891967&to=2893603)