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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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| Huvudupphovsmän: | , |
|---|---|
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
1986
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC339841/ https://ncbi.nlm.nih.gov/pubmed/3012460 |
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