Abstract
Plasmids are convenient vectors for the maintenance of cloned DNA. Inserts are stable, and large amounts of double-stranded (ds) DNA can be purified easily, manipulated in vitro with restriction and ligation enzymes, and the recombinant constructs reintroduced with high efficiency into E. coli by transformation.
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Cesareni, G., Murray, J.A.H. (1987). Plasmid Vectors Carrying the Replication Origin of Filamentous Single-Stranded Phages. In: Setlow, J.K. (eds) Genetic Engineering. Genetic Engineering. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5377-5_9
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DOI: https://doi.org/10.1007/978-1-4684-5377-5_9
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