In article <199501272030.OAA17990 at molbio.cbs.umn.edu>, shin at MOLBIO.CBS.UMN.EDU ("shin enomoto") writes:
>I need to sequence inserts cloned into pBM272, a GAL1-10 promoter expression
>vector. I would like to know if there is a true and tried sequencing primer
>going outward from the GAL promoters sequence.
>>Shin Enomoto
>Dept. Plant Biol.
>Univ. Minnesota
>220 Biol. Sci. Cent.
>1445 Gortner Ave.
>St. Paul, MN 55108
>612/625-9786
I use oligo corresponding to GAL1 leader , 5'-cct cta tac ttt aac gtc-3'. It
begins about 25nt downstream from GAL1 transcription start point acc. to
Johnston, Davis MCB 4:1440-1448, 1984, and ends about 10 nt upstream from
the BamHI site created in this work and usually used to make GAL1 promoter
vectors.
Hope this helps
Dima Belostosky
>
