Efficient and accurate in vitro processing of simian virus 40-associated small RNA.
Nuclei were isolated from simian virus 40 (SV40)-infected cells with a hypotonic, detergent-free buffer and incubated in vitro in a high-ionic-strength buffer containing [alpha-32P]UTP. The labeled viral RNAs produced were analyzed by gel electrophoresis together with 3-h-labeled viral RNAs extracte...
Збережено в:
| Опубліковано в:: | J Virol |
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| Автори: | , , |
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
American Society for Microbiology (ASM)
1986
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| Предмети: | |
| Онлайн доступ: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC252746/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3001362/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.57.1.402-407.1986 |
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