HSV helper virus independent vector

Chemistry: molecular biology and microbiology – Treatment of micro-organisms or enzymes with electrical or... – Modification of viruses

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435 691, 435320, 4352402, 935 29, 935 32, 935 34, 935 70, C12N 510, C12N 701, C12N 1538, C12N 1586

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active

049701550

ABSTRACT:
This invention encompasses an eukaryotic expression vector constructed from a prokaryotic plasmid by inserting into the prokaryotic plasmid a mediator sequence and a promoter/regulatory sequence with a restriction endonuclease site for inserting a gene to be expressed. The gene to be expressed is inserted into the restriction endonuclease site in the promoter/regulatory sequence and the resulting plasmid is in turn used to transform a eukaryotic cell. The gene is expressed with or without viral mediation.

REFERENCES:
Stow, N. et al. in Eukaryotic Expression Vectors (ed Y. Gluzman), Cold Spring Harbor Laboratory, pp. 199-204, 1982.
Stow, N., The Embo Journal, vol. 1, No. 7, pp. 863-867, 1982.
Dubois, M., et al, Proc. Natl. Acad Sci, vol. 77, No. 8, pp. 4549-4553, 1980.
Burrell, C. J. et al., Nature, vol. 279, pp. 43-47, 1979.
Enquist, L. et al., Genevol. 7, pp. 335-342, 1979.
Post, Leonard E., et al., "A Generalized Technique for Deletion of Specific Genes in Large Genomes: .alpha.Gene 22 of Herpes Simplex Virus 1 is Not Essential for Growth," CELL, vol. 25, 227-232, Jul. 1981.

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