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Revision as of 17:15, 7 March 2010 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[413-470], a partially-truncated VP16 transactivation domain), using primers that add att sites, followed by a BP reaction. Sequencing finds a single silent mutation, G1114T.

Sequence

Annotated sequence, Genbank format:
pME-Gal4VP16 Genbank

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