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m (Sequence)
(Construction details)
 
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p5E-bactin2 was made by PCR of the ''bactin2'' upstream genomic sequence (using primers to add att sites),
 
p5E-bactin2 was made by PCR of the ''bactin2'' upstream genomic sequence (using primers to add att sites),
followed by a BP reaction. Upstream sequence includes 3.8 kb upstream of transcriptional start, a small 5. UTR exon, a 1.4 kb intron, and then 38 bp of 5' UTR,
+
followed by a BP reaction. Upstream sequence includes 3.8 kb upstream of transcriptional start, a small 5' UTR exon, a 1.4 kb intron, and then 38 bp of 5' UTR,
 
terminating immediately before the native start codon.
 
terminating immediately before the native start codon.
 
Sequencing confirms that the ends of the insert are correct.
 
Sequencing confirms that the ends of the insert are correct.

Latest revision as of 17:34, 22 August 2008

Construction details

bactin2 genomic sequence was derived from a 5.3 kb clone (gift of Ken Poss), which was derived in turn from a 10 kb upstream construct from Shin-ichi Higashijima.

p5E-bactin2 was made by PCR of the bactin2 upstream genomic sequence (using primers to add att sites), followed by a BP reaction. Upstream sequence includes 3.8 kb upstream of transcriptional start, a small 5' UTR exon, a 1.4 kb intron, and then 38 bp of 5' UTR, terminating immediately before the native start codon. Sequencing confirms that the ends of the insert are correct.

Reference

Higashijima S, Okamoto H, Ueno N, Hotta Y, Eguchi G. (1997) Dev Biol.15;192:289-99. "High-frequency generation of transgenic zebrafish which reliably express GFP in whole muscles or the whole body by using promoters of zebrafish origin."

Sequence

Annotated sequence, Genbank format:
p5E-bactin2 Genbank

FASTA file with the full-length sequence as well as sequences of individual components:
p5E-bactin2 sequence

Crude map

Screenshot from Sequencher showing locations of components:
P5E-bactin2.png