A versatile phage lambda expression vector system for cloning in Escherichia coli
- 1 February 1989
- Vol. 75 (2) , 261-270
- https://doi.org/10.1016/0378-1119(89)90272-2
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- The mob and oriT mobilization functions of a bacterial plasmid promote its transfer to plantsNature, 1987
- Mobilization of the non-conjugative plasmid RSF1010: A genetic analysis of its origin of transferMolecular Genetics and Genomics, 1987
- Molecular cloning of the plasmid RP4 primase region in a multi-host-range tacP expression vectorGene, 1986
- A comprehensive set of sequence analysis programs for the VAXNucleic Acids Research, 1984
- Activity of the hybrid trp-lac (tac) promoter of Escherichia coli in Pseudomonas putida. Construction of broad-host-range, controlled-expression vectorsGene, 1983
- Vectors bearing a hybrid trp-lac promoter useful for regulated expression of cloned genes in Escherichia coliGene, 1983
- Compilation and analysis ofEscherichia colipromoter DNA sequencesNucleic Acids Research, 1983
- Specific-purpose plasmid cloning vectors II. Broad host range, high copy number, RSF 1010-derived vectors, and a host-vector system for gene cloning in PseudomonasGene, 1981
- Improvements of DNA sequencing gelsAnalytical Biochemistry, 1981
- A complementation analysis of the restriction and modification of DNA in Escherichia coliJournal of Molecular Biology, 1969