Stable high-copy-number bacteriophage λ promoter vectors for overproduction of proteins in Escherichia coli
- 1 October 1996
- Vol. 176 (1-2) , 49-53
- https://doi.org/10.1016/0378-1119(96)00208-9
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Affinity purification of histidine-tagged proteinsMolecular Biology Reports, 1993
- The 92-min region of the Escherichia coli chromosome: location and cloning of the ubi and alrGene, 1993
- A fully modular vector system for the optimization of gene expression in Escherichia coliPlasmid, 1991
- Modified bacteriophage lambda promoter vectors for overproduction of proteins in Escherichia coliGene, 1990
- The pMTL nic− cloning vectors. I. Improved pUC polylinker regions to facilitate the use of sonicated DNA for nucleotide sequencingGene, 1988
- New metal chelate adsorbent selective for proteins and peptides containing neighbouring histidine residuesJournal of Chromatography A, 1987
- Inducible expression vectors incorporating the Escherichia coli atpE translational initiation regionGene, 1987
- Plasmid vector pBR322 and its special-purpose derivatives — a reviewGene, 1986
- The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primersGene, 1982
- Metal chelate affinity chromatography, a new approach to protein fractionationNature, 1975