作者: HANS Stahl , P Dröge , HANSWALTER Zentgraf , ROLF Knippers , None
DOI: 10.1128/JVI.54.2.473-482.1985
关键词:
摘要: In productively infected cells, a fraction of large-tumor antigen (T antigen) is tightly bound to replicating simian virus 40 (SV40) minichromosomes and does not dissociate at salt concentrations greater than 1 M NaCl. We present electronmicrograms demonstrating the presence T on replicated sections SV40 minichromosomes. also show that recognized by antibodies from mouse tumor serum and, more specifically, particular T-antigen-specific monoclonal antibody, PAb 1630. A second 101, react with T-antigen remaining chromatin high concentrations. used an in vitro replication system which allows, via semiconservative DNA replication, completion vivo-initiated replicative intermediate molecules. antibody 1630, but inhibits viral replication. discuss possibility may play role chain elongation during