From Tol2Kit
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The mCherry sequence includes a start codon but '''not''' a good Kozak consensus (unlike p3E-EGFP-pA, which has both). | The mCherry sequence includes a start codon but '''not''' a good Kozak consensus (unlike p3E-EGFP-pA, which has both). | ||
| − | === | + | === Sequence === |
| + | Annotated sequence, Genbank format:<br> | ||
| + | [[p3E-mCherrypA Genbank]] | ||
| + | |||
FASTA file with the full-length sequence as well as sequences of individual components:<br> | FASTA file with the full-length sequence as well as sequences of individual components:<br> | ||
[[p3E-mCherrypA sequence]] | [[p3E-mCherrypA sequence]] | ||
Latest revision as of 03:53, 19 December 2007
Construction details
p3E-mCherrypA was made by PCR amplification of mCherry and an SV40 late polyadenylation signal from a pCS2+-based construct, using primers to add att sites, followed by a BP reaction. Sequencing finds a single base PCR error, encoding an E7D mutation in mCherry. Functional tests of C-terminal fusion proteins made with this construct show that they yield fluorescent protein.
The mCherry sequence includes a start codon but not a good Kozak consensus (unlike p3E-EGFP-pA, which has both).
Sequence
Annotated sequence, Genbank format:
p3E-mCherrypA Genbank
FASTA file with the full-length sequence as well as sequences of individual components:
p3E-mCherrypA sequence
Crude map
Screenshot from Sequencher showing locations of components:
