Construction of versatile low-copy-number vectors for cloning, sequencing and gene expression in Escherichia coli

This publication has 15 references indexed in Scilit:

• Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
  Science, 1988
• λ ZAP: a bacteriophage λ expression vector within vivoexcision properties
  Nucleic Acids Research, 1988
• [58] Direct sequencing of denatured plasmid DNA
  Published by Elsevier ,1987
• Single-stranded DNA ‘blue’ T7 promoter plasmids: a versatile tandem promoter system for cloning and protein engineering
  Protein Engineering, Design and Selection, 1986
• Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectors
  Gene, 1985
• Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing
  Gene, 1984
• The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers
  Gene, 1982
• Versatile low-copy-number plasmid vectors for cloning in Escherichia coli
  Gene, 1982
• Characterization of the dnaA, gyrB and other genes in the dnaA region of the Escherichia coli chromosome on specialized transducing phages λtna
  Molecular Genetics and Genomics, 1979
• Characterization of λpolA transducing phages; Effective expression of the E. coli polA gene
  Molecular Genetics and Genomics, 1979