Construction of β-lactamase-encoding ApR gene cassettes for rapid identification of cloned genes

Gene

Volumn 170, Issue 1, 1996, Pages 143-144

  Yokochi, Tomoki ^a   Kato, Jun Ichi ^a   Ikeda, Hideo ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

DNA sequencing; pUC plasmid primer; Recombinant DNA tool

Indexed keywords

ESCHERICHIA COLI;

BETA LACTAMASE; RECOMBINANT DNA;

ARTICLE; DNA SEQUENCE; ESCHERICHIA COLI; GENE SEQUENCE; GENETIC ANALYSIS; NONHUMAN; PLASMID; PRIORITY JOURNAL; TECHNIQUE;

AMPICILLIN RESISTANCE; BACTERIAL PROTEINS; CLONING, MOLECULAR; DNA PRIMERS; DNA, BACTERIAL; DNA, RECOMBINANT; ESCHERICHIA COLI; GENES; GENETIC VECTORS; PENICILLINASE;

EID: 0029872941     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/0378-1119(95)00826-8     Document Type: Article

References (4)

1. Kato, J., Nishimura, Y., Yamada, M., Suzuki, H. and Hirota, Y.: Gene organization in the region containing a new gene involved in chromosome partition in Escherichia coli. J. Bacteriol. 170 (1988) 3967-3977.
2. Sambrook, J., Fritsch, E.F. and Maniatis, T.: Molecular Cloning. A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989.
3. Vieira, J. and Messing, J.: The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene 19 (1982) 259-268.
4. Yanisch-Perron, C., Vieira, J. and Messing, J.: Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene 33 (1985) 103-119.