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Titlebook: CRISPR-Cas Methods; Volume 2 M. Tofazzal Islam,Kutubuddin Ali Molla Book 2021 The Editor(s) (if applicable) and The Author(s), under exclus

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发表于 2025-3-21 17:21:32 | 显示全部楼层 |阅读模式
书目名称CRISPR-Cas Methods
副标题Volume 2
编辑M. Tofazzal Islam,Kutubuddin Ali Molla
视频videohttp://file.papertrans.cn/221/220558/220558.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
丛书名称Springer Protocols Handbooks
图书封面Titlebook: CRISPR-Cas Methods; Volume 2 M. Tofazzal Islam,Kutubuddin Ali Molla Book 2021 The Editor(s) (if applicable) and The Author(s), under exclus
描述.This second volume provides new and updated methods detailing advancements in CRISPR-Cas technical protocols. Chapters guide readers through protocols on prime editing, base editing, multiplex editing, editing in cell-free extract, in silico analysis of gRNA secondary structure and CRISPR-diagnosis.  .. Authoritative and cutting-edge,  .CRISPR-Cas Methods, Volume 2. aims to serves as a laboratory manual providing scientists with a  holistic view of CRISPR-Cas methodologies and its practical application for the editing of crop plants, cell lines, nematode and microorganism..The chapter “CRISPR/Cas9-mediated gene editing in human induced pluripotent stem cells” is available open access under a Creative Commons Attribution 4.0 International License via link.springer.com..
出版日期Book 2021
关键词Maize; Potato; Cytosine; Prime editing; CRISPR activator
版次1
doihttps://doi.org/10.1007/978-1-0716-1657-4
isbn_softcover978-1-0716-1659-8
isbn_ebook978-1-0716-1657-4Series ISSN 1949-2448 Series E-ISSN 1949-2456
issn_series 1949-2448
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Science+Busines
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发表于 2025-3-21 20:18:54 | 显示全部楼层
Chr. Gutenbrunner,G. Hildebrandtew crop variety. This chapter briefly describes the methods of CRISPR-Cas9 vector construction with single and multiple gene targets in rice. The protocol covers all important steps of target sequence selection, single/multiple-target vector construction, mutation detection, and selection of T-DNA free mutant lines.
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In Vitro Cas9 Cleavage Assay to Check Guide RNA Efficiency,ro method to screen multiple sgRNAs to identify the most suitable one that can efficiently introduce a double-stranded break at a particular genomic target site. This screening method allows a researcher to choose the best one among several online predicted sgRNAs prior to deliver genome editing reagents into live plant or animal cells.
发表于 2025-3-22 18:34:18 | 显示全部楼层
Generation of Knockout and Fragment Deletion Mutants in Soybean by CRISPR-Cas9,o the CRISPR-Cas9-mediated targeted mutagenesis or large fragment deletions in soybean. Detailed procedures will guide through the essential steps including the design of sgRNAs, construction of CRISPR-Cas9 vectors, .-mediated soybean transformation, and identification of mutant lines.
发表于 2025-3-23 00:39:44 | 显示全部楼层
1949-2448 ation advice from the experts.This second volume provides new and updated methods detailing advancements in CRISPR-Cas technical protocols. Chapters guide readers through protocols on prime editing, base editing, multiplex editing, editing in cell-free extract, in silico analysis of gRNA secondary s
发表于 2025-3-23 02:38:36 | 显示全部楼层
https://doi.org/10.1007/978-3-662-25284-0e, wheat, maize, and tomato, which substantially expands the scope and capabilities of precision plant breeding. Here, we describe a fast and efficient method for construction of prime editing vectors based on Gateway assembly and efficiency assessment of prime editors through transient expression analyses in rice protoplasts.
发表于 2025-3-23 07:41:14 | 显示全部楼层
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