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The Absence of Mutagenic Activity of Benzidine and 4,4″-Diaminoterphenyl in Tk6 Human Lymphoblast Cells

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Comparative Genetic Toxicology

Abstract

The human lymphoblast line TK6, heterozygous at the thymidine kinase locus, has been developed for use as a mutation assay by Thilly and co-workers (Thilly et al., 1980; Liber and Tilley, 1982; Deluca et al., 1983 and Goldmacher et al., 1983). The cells grow in suspension culture and may be readily cloned with high efficiency using the microtitration method. We have selected for resistance to 6-thioguanine, trifluorothymidine and ouabain to test the mutagenic response of Tk6 cells following treatment with benzidine (BZD) and 4,4″-diaminotherphenyl (DAT). Experiments were carried out with and without Aroclor-induced rat S9 liver supernatant.

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© 1985 United Kingdom Environmental Mutagen Society

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Cole, J., Arlett, C.F., Muriel, W.J. (1985). The Absence of Mutagenic Activity of Benzidine and 4,4″-Diaminoterphenyl in Tk6 Human Lymphoblast Cells. In: Parry, J.M., Arlett, C.F. (eds) Comparative Genetic Toxicology. Palgrave Macmillan, London. https://doi.org/10.1007/978-1-349-07901-8_35

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