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Organization of type C viral DNA sequences endogenous to baboons: analysis with cloned viral DNA
Journal of Virology, 1982Unintegrated linear and circular forms of baboon endogenous type C virus M7 DNA were prepared from M7-infected cells by chromatography on hydroxyapatite columns, and the circular DNAs were purified in cesium chloride-ethidium bromide equilibrium density gradients. The circular DNAs were linearized by digestion with EcoRI, which had a unique site on the
N, Battula, G L, Hager, G J, Todaro
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Viral Vaccines and Residual Cellular DNA
Biologicals, 1995The acceptability of viral vaccines manufactured in culture of continuous cell lines opened the way to a new technology of vaccine preparation. The large scale cultivation of continuous cell lines contributed greatly to the improvement of the safety and the consistency of viral vaccines.
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Branched DNA for Quantification of Viral LOAD
Immunological Investigations, 1997This is a summary of a presentation made at the 13th International Convocation on Immunology. Nucleic acids in patient samples can be quantified directly using a solid phase nucleic acid hybridization assay based on branched DNA (bDNA) signal amplification technology.
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Integration of Viral DNA into the Host Genome
1975Animal viruses can interact with their host cells in different ways: (1) The virus can actively replicate and finally destroy the cell in a lytic or productive infection. (2) The infection can become abortive or non-productive and lead to the apparent or inapparent persistence or the eventual loss of the viral genome.
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The Anatomy of Viral DNA Molecules
Annual Review of Biochemistry, 1967C A, Thomas, L A, MacHattie
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