Krawetz S A, Sellos D, Wong N C, Dixon G H
Department of Medical Biochemistry, Faculty of Medicine, University of Calgary, Alberta, Canada.
Gene. 1989 Oct 30;82(2):317-20. doi: 10.1016/0378-1119(89)90057-7.
A phagemid was adapted for use as the vector in the vector-primer-cloner-sequencer cloning system. The use of this new vector markedly expanded the utility of this technology for the construction of cDNA libraries. Technological advantages and new capabilities include: (1) a greater number of unique restriction sites within the polylinker region; (2) the ability to produce single-stranded templates for nucleotide sequencing, and (3) a convenient means to synthesize strand-specific hybridization probes. With the use of this cloning system, a rat liver cDNA library (8.56 x 10(5) recombinants from 1 microgram of poly(A)+ RNA) was rapidly (in two days) constructed.