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Titlebook: DNA Damage Responses; Methods and Protocol Nima Mosammaparast Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive li

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發(fā)表于 2025-3-21 19:31:17 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱DNA Damage Responses
副標(biāo)題Methods and Protocol
編輯Nima Mosammaparast
視頻videohttp://file.papertrans.cn/261/260136/260136.mp4
概述Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
叢書(shū)名稱Methods in Molecular Biology
圖書(shū)封面Titlebook: DNA Damage Responses; Methods and Protocol Nima Mosammaparast Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive li
描述.This volume provides detailed methods and key approaches used to .m.echanistically study DNA damage, as well as the factors involved in the damage response. Chapters guide readers through proteomics and biophysical approaches, analyzing protein function, quantifying DNA replication dynamics and nucleic acid base damage, as well as biochemical reconstitution of key pathways involved in DNA repair. Written in the highly successful .Methods in Molecular Biology. series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..?Authoritative and cutting-edge, .DNA Damage Responses: Methods and Protocols .aims to be a useful practical guide to researches to help further their study in this field..
出版日期Book 2022
關(guān)鍵詞mass spectrometry; cytosine deaminases; DNA damage response; CRISPR/Cas9; chemoptogenetics
版次1
doihttps://doi.org/10.1007/978-1-0716-2063-2
isbn_softcover978-1-0716-2065-6
isbn_ebook978-1-0716-2063-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
The information of publication is updating

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Purification of DNA-Dependent Protein Kinase Catalytic Subunit (DNA-PKcs) from HeLa Cells,r, DNA-PKcs is relatively abundant in human cells, making it possible to purify the endogenous protein. Here we describe a method to purify DNA-PKcs and its binding partner Ku70/80 from HeLa cells and describe conditions for transfer of DNA-PKcs and other large polypeptides for immunoblotting.
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Richard W. Eglese,Adam N. Letchford, which is termed termination, is relatively unexplored. Our knowledge of termination is limited by cellular approaches to study DNA replication, which cannot readily detect termination. In contrast, the . egg extract system allows for all of DNA replication to be readily detected. Here we describe
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