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4. A cloning vector for creation of Escherichia coli lacZ translational fusions and generation of linear template for chromosomal integration. Uhlich GA; Chen CY Plasmid; 2012 May; 67(3):259-63. PubMed ID: 22197962 [TBL] [Abstract][Full Text] [Related]
5. [The use of the multicopy plasmid pUC19 for assuring the constitutive expression of gene rplL in Escherichia coli]. Zolotukhin SB; Zhivolup AN; Krupskaia IV; Budmaska MI; Paton EB Tsitol Genet; 1989; 23(6):22-4. PubMed ID: 2516378 [TBL] [Abstract][Full Text] [Related]
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11. Coupling the T7 A1 promoter to the runaway-replication vector as an efficient method for stringent control and high-level expression of lacZ. Chao YP; Chern JT; Wen CS Biotechnol Prog; 2001; 17(1):203-7. PubMed ID: 11170500 [TBL] [Abstract][Full Text] [Related]
12. New cloning vectors for integration in the lambda attachment site attB of the Escherichia coli chromosome. Diederich L; Rasmussen LJ; Messer W Plasmid; 1992 Jul; 28(1):14-24. PubMed ID: 1387714 [TBL] [Abstract][Full Text] [Related]
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18. [Cloning the uridine phosphorylase (udp) gene of Escherichia coli and its expression in recombinant plasmids]. Brikun IA; Mironov AS; Sukhodolets VV; Khurges EM Genetika; 1989 Oct; 25(10):1717-24. PubMed ID: 2515986 [TBL] [Abstract][Full Text] [Related]
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20. [Plasmid expression vectors with elements of the E. coli alkaline phosphatase gene]. Zozulia SA; Obukhova TA; Shirokova EP; Babalov PR Bioorg Khim; 1990 Oct; 16(10):1339-47. PubMed ID: 2150748 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]