Use of a modified Escherichia coli trpR gene to obtain tight regulation of high-copy-number expression vectors
- 31 December 1985
- Vol. 46 (1) , 103-112
- https://doi.org/10.1016/0378-1119(86)90172-1
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Regulated high-level expression of the Herpes simplex type I thymidine kinase gene in Escherichia coliGene, 1984
- High-copy-number derivatives of the plasmid cloning vector pBR322Gene, 1984
- Toxicity of an overproduced foreign gene product in Escherichia coli and its use in plasmid vectors for the selection of transcription terminatorsGene, 1984
- Analysis in vivo of factors affecting the control of transcription initiation at promoters containing target sites for Trp repressorMolecular Genetics and Genomics, 1984
- Construction and characterization of the chloramphenicol-resistance gene cartridge: A new approach to the transcriptional mapping of extrachromosomal elementsGene, 1982
- The complete amino acid sequence of human fibroblast interferon as deduced using synthetic oligodeoxyribonucleotide primers of reverse transcriptaseNucleic Acids Research, 1980
- A rapid alkaline extraction procedure for screening recombinant plasmid DNANucleic Acids Research, 1979
- Structural and functional analysis of cloned deoxyribonucleic acid containing the trpR-thr region of the Escherichia coli chromosomeJournal of Bacteriology, 1979
- [17] Plasmid cloning vehicles derived from plasmids ColE1, F, R6K, and RK2Published by Elsevier ,1979
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970