An improved Escherichia coli expression vector for the construction and identification of full-length cDNA clones
- 1 January 1986
- Vol. 44 (2-3), 347-351
- https://doi.org/10.1016/0378-1119(86)90201-5
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Direct immunological identification of full‐length cDNA clones for plant protein without gene fusion to E. coli proteinFEBS Letters, 1986
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Molecular cloning and nucleotide sequence of cDNA for sporamin, the major soluble protein of sweet potato tuberous rootsPlant Molecular Biology, 1985
- Efficientin vitrosynthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoterNucleic Acids Research, 1984
- Efficient isolation of genes by using antibody probes.Proceedings of the National Academy of Sciences, 1983
- Identification of clones that encode chicken tropomyosin by direct immunological screening of a cDNA expression library.Proceedings of the National Academy of Sciences, 1983
- The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primersGene, 1982
- High-efficiency cloning of full-length cDNA.Molecular and Cellular Biology, 1982
- Synthesis of human fibroblast interferon by E. coliNucleic Acids Research, 1980
- Immunological screening method to detect specific translation products.Proceedings of the National Academy of Sciences, 1978