Description of a one step staggered reannealing method for directional cloning of PCR-generated DNA using sticky-end ligation without employing restriction enzymes
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Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter
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A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors
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Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products
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Minimum duplex requirements for restriction enzyme cleavage near the termini of linear DNA fragments
Moreira R.F., and Noren C.J. Minimum duplex requirements for restriction enzyme cleavage near the termini of linear DNA fragments. Biotechniques 19 (1995) 56-59
The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers
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Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectors
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