[5] Use of Escherichia coli trp promoter for direct expression of proteins
- 1 January 1990
- book chapter
- Published by Elsevier
- Vol. 185, 54-60
- https://doi.org/10.1016/0076-6879(90)85007-b
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Use of a modified Escherichia coli trpR gene to obtain tight regulation of high-copy-number expression vectorsGene, 1985
- Purification and immunogenicity of fusion VP1 protein of foot and mouth disease virusBiochemistry, 1984
- Efficient Expression inEscherichia coliof a Mature and a Modified Human Interferon-β1DNA, 1984
- The influence of messenger RNA secondary structure on expression of an immunoglobulin heavy chain inEscherichia coliNucleic Acids Research, 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 Application of a Novel Plasmid "ATG Vector" for Direct Expression of Foreign Genes inEscherichia coliDNA, 1983
- Expression of human immune interferon cDNA in E. coli and monkey cellsNature, 1982
- Increased Synthesis inE. coliof Fibroblast and Leukocyte Interferons Through Alterations in Ribosome Binding SitesDNA, 1982
- Human leukocyte interferon produced by E. coli is biologically activeNature, 1980
- Plasmid vectors containing the tryptophan operon promoter suitable for efficient regulated expression of foreign genesGene, 1980