P3E-EGFPpA: Difference between revisions

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Created page with "== Construction Details == This template is used to display DNA sequence information in a standardized format. == Crude Map == photo showing locations of components == Sequence == * Annotated Sequence: (Genbank format) link * Full-Length Sequence with individual component sequences included: (FASTA file) link == Reference == This template is used to display DNA sequence information in a standardized format."
 
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== Construction Details ==
== Construction Details ==
This template is used to display DNA sequence information in a standardized format.
p3E-EGFPpA was made by PCR amplification of EGFP and an SV40 late polyadenylation signal from a pCS2+-based plasmid, using primers to add att sites, followed by a BP reaction.


== Crude Map ==
Note that the EGFP sequence is followed by 60 bp of polylinker sequence from pCS2+ before the stop codon. We have confirmed functionally that this cassette produces fluorescent protein in C-terminal fusion constructs. Sequencing confirms that all bases of the insert are correct.
photo showing locations of components


== Sequence ==
The EGFP sequence does include a start codon and a good Kozak consensus, so it is possible to use this clone to test promoters cloned into a middle clone.
* Annotated Sequence: (Genbank format)
link
 
* Full-Length Sequence with individual component sequences included: (FASTA file)
link


== Crude Map ==
Screenshot from Sequencher showing locations of components:
P3E-EGFPpA.png


== Reference ==
==Download the Sequence ==
This template is used to display DNA sequence information in a standardized format.
* '''Annotated Sequence'''(Genbank format) and '''Full-Length Sequence with individual component sequences included'''(FASTA file)
: [[Media:366.p3E-EGFPpA.zip|Download p3E-EGFPpA]]

Revision as of 16:26, 13 March 2025

Construction Details

p3E-EGFPpA was made by PCR amplification of EGFP and an SV40 late polyadenylation signal from a pCS2+-based plasmid, using primers to add att sites, followed by a BP reaction.

Note that the EGFP sequence is followed by 60 bp of polylinker sequence from pCS2+ before the stop codon. We have confirmed functionally that this cassette produces fluorescent protein in C-terminal fusion constructs. Sequencing confirms that all bases of the insert are correct.

The EGFP sequence does include a start codon and a good Kozak consensus, so it is possible to use this clone to test promoters cloned into a middle clone.

Crude Map

Screenshot from Sequencher showing locations of components: P3E-EGFPpA.png

Download the Sequence

  • Annotated Sequence(Genbank format) and Full-Length Sequence with individual component sequences included(FASTA file)
Download p3E-EGFPpA