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(New page: === Construction details === pME-EGFP no stop was made by PCR amplification of the EGFP insert from a pCS2-based plasmid, using primers that add att sites, followed by a BP reaction. Sequ...)
 
 
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This clone can be used to generate N-terminal EGFP fusions with a gene of interest placed in a 3' clone.
 
This clone can be used to generate N-terminal EGFP fusions with a gene of interest placed in a 3' clone.
  
=== Crudely annotated sequence ===
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=== Sequence ===
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Annotated sequence, Genbank format:<br>
 +
[[pME-EGFP no stop Genbank]]
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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>
 
[[pME-EGFP no stop sequence]]
 
[[pME-EGFP no stop sequence]]

Latest revision as of 03:48, 19 December 2007

Construction details

pME-EGFP no stop was made by PCR amplification of the EGFP insert from a pCS2-based plasmid, using primers that add att sites, followed by a BP reaction. Sequencing confirms that all bases of the insert are correct.

This clone can be used to generate N-terminal EGFP fusions with a gene of interest placed in a 3' clone.

Sequence

Annotated sequence, Genbank format:
pME-EGFP no stop Genbank

FASTA file with the full-length sequence as well as sequences of individual components:
pME-EGFP no stop sequence

Crude map

Screenshot from Sequencher showing locations of components:
PME-EGFP no stop.png