Difference between revisions of "Part:BBa K3165046"
| Line 4: | Line 4: | ||
i^2mCherry overcomes the deficiencies in the existing mCherry sequences which undergoes significant truncation in the protein. The single-base mutation at the 48th base causes conversion of the internal start codon into ATC (coding for Ile). | i^2mCherry overcomes the deficiencies in the existing mCherry sequences which undergoes significant truncation in the protein. The single-base mutation at the 48th base causes conversion of the internal start codon into ATC (coding for Ile). | ||
| − | <html><a href="https://www.ncbi.nlm.nih.gov/pubmed/11753367"></a></html> | + | <html><a href="https://www.ncbi.nlm.nih.gov/pubmed/11753367">abc</a></html> |
| + | |||
<!-- --> | <!-- --> | ||
<span class='h3bb'><b>Sequence and Features</b></span> | <span class='h3bb'><b>Sequence and Features</b></span> | ||
Revision as of 09:49, 20 October 2019
i^2mCherry (Ile) Coding Device (under T7 expression)
i^2mCherry overcomes the deficiencies in the existing mCherry sequences which undergoes significant truncation in the protein. The single-base mutation at the 48th base causes conversion of the internal start codon into ATC (coding for Ile). abc
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 738
- 1000COMPATIBLE WITH RFC[1000]