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Plasmid and bacteriophage vectors for excision of intact inserts
R Lathe1, J L Vilotte, A J Clark
1LGME-CNRS, Strasbourg, France.
Gene
|January 1, 1987
Abstract:
Plasmid (pPolyIII) and bacteriophage lambda (EMBL301) vectors are described in which sites for the rare-cutting enzymes SfiI and NotI (8-bp, recognition sequences) flank the polylinker cloning region. Intact DNA inserts for introduction into cultured cells or into the early embryo are readily excised from the vectors. General-purpose miniplasmid cloning vectors pPolyI and pPolyII are also described, and the utility of the bacteriophage lambda vector is demonstrated in the construction of a bovine genomic library.