Highly selective chemical modification of cruciform loops by diethyl pyrocarbonate.
Diethyl pyrocarbonate reacts with the single-stranded loops of cruciform structures with great selectivity. Adenine bases are carbethoxylated, as a result of which the backbone may be cleaved with piperidine, and the level of chemical modification at each base may be determined. We have studied the...
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| Pubblicato in: | Nucleic Acids Res |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
1986
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| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC339841/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3012460/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/14.10.3995 |
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