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Live cell monitoring of double strand breaks in S. cerevisiae
We have used two different live-cell fluorescent protein markers to monitor the formation and localization of double-strand breaks (DSBs) in budding yeast. Using GFP derivatives of the Rad51 recombination protein or the Ddc2 checkpoint protein, we find that cells with three site-specific DSBs, on di...
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| Veröffentlicht in: | PLoS Genet |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6415866/ https://ncbi.nlm.nih.gov/pubmed/30822309 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1008001 |
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