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Titlebook: R-Loops; Methods and Protocol Andrés Aguilera,Alexey Ruzov Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive licen

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51#
發(fā)表于 2025-3-30 08:25:25 | 只看該作者
52#
發(fā)表于 2025-3-30 13:27:28 | 只看該作者
,Studies on Protein–RNA:DNA Hybrid Interactions by Microscale Thermophoresis (MST), of the interaction of the N-terminal his-tagged 6-methyladenine (m.A) reader protein YTHDF2 with m.A modified and unmodified RNA, in single-strand configuration or with RNA:DNA hybrid substrates. The described protocol is also suitable for studies of interactions with proteins binding to double-stranded RNA or DNA substrates.
53#
發(fā)表于 2025-3-30 17:23:56 | 只看該作者
54#
發(fā)表于 2025-3-30 22:24:08 | 只看該作者
Book 2022allowing for the detection of DNA-RNA hybrids, as well as their purification and visualization by electron microscopy, the volume continues with methods based on the use of RNase H-derived tools to detect DNA-RNA hybrids .in vitro. and .in vivo.. Several protocols permit studying non-canonical RNA n
55#
發(fā)表于 2025-3-31 03:46:05 | 只看該作者
Detection of R-Loops by In Vivo and In Vitro Cytosine Deamination in , genome integrity. Here, we describe the protocols used in the yeast . to infer the presence of?R-loops through increased AID-induced DNA damage, measured as increased recombination or Rad52 foci formation as well as to detect single R-loop molecules and determine their length at particular genomic sites via bisulfite treatment and amplification.
56#
發(fā)表于 2025-3-31 06:11:26 | 只看該作者
57#
發(fā)表于 2025-3-31 09:36:34 | 只看該作者
58#
發(fā)表于 2025-3-31 16:00:14 | 只看該作者
59#
發(fā)表于 2025-3-31 18:46:32 | 只看該作者
,RNase H1 Hybrid-Binding Domain-Based Tools for Cellular Biology Studies of DNA–RNA Hybrids in Mammanowledge about R loops and factors associated with their formation and removal. Here, we describe the use of fluorescently tagged HBD, the hybrid-binding domain of RNase H1, as a tool for analyzing DNA–RNA hybrids in different contexts using live-cell microscopy and immunofluorescence experiments.
60#
發(fā)表于 2025-3-31 22:37:40 | 只看該作者
,DNA–RNA Hybrids at Telomeres in Budding Yeast,ect recovered material, and furthermore allows the precipitation of other proteins from the identical cross-linked material. Although both methods are successful in terms of detecting DNA–RNA hybrids at telomeres, the R-ChIP method yields an approximately ten-fold increased enrichment.
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