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Revision as of 02:18, 24 March 2007 by Chi-bin (talk | contribs) (Construction details)

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Construction details

pME-Gal4VP16 was made by PCR amplification of Gal4VP16 (Gal4 DNA binding domain fused to VP16 transactivation domain), using primers that add att sites, followed by a BP reaction. Sequencing finds a single silent mutation, G1114T.

Crudely annotated sequence

FASTA file with the full-length sequence as well as sequences of individual components:
pME-Gal4VP16 sequence

Crude map

Screenshot from Sequencher showing locations of components:
PME-Gal4VP16.png