Control of cloned gene expression by promoter inversion in vivo: construction of improved vectors with a multiple cloning site and the ptac promoter
- 1 January 1987
- Vol. 56 (1) , 145-151
- https://doi.org/10.1016/0378-1119(87)90167-3
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Effect of the promoter structure on the nutL transcription antitermination functionGene, 1986
- Boundaries of the nutL antiterminator of coliphage lambda and effects of mutations in the spacer region between boxA and boxBGene, 1986
- A novel multistep method for generating precise unidirectional deletions using BspMI, a class-IIS restriction enzymeGene, 1986
- Control of cloned gene expression by promoter inversion in vivo: construction of the heat-pulseactivated att-nutL-p-att-N moduleGene, 1985
- The extent of DNA sequence required for a functional bacterial attachment site of phage lambdaNucleic Acids Research, 1985
- The pIC plasmid and phage vectors with versatile cloning sites for recombinant selection by insertional inactivationGene, 1984
- Construction and analysis of in vivo activity of E. coll promoter hybrids and promoter mutants that alter the −35 to −10 spacingGene, 1982
- INTEGRATION AND EXCISION OF BACTERIOPHAGE λ: THE MECHANISM OF CONSERVATIVE SITE SPECIFIC RECOMBINATIONAnnual Review of Genetics, 1981
- Plasmids containing many tandem copies of a synthetic lactose operatorGene, 1980