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Titlebook: CRISPR; Methods and Protocol Magnus Lundgren,Emmanuelle Charpentier,Peter C. Fi Book 2015 Springer Science+Business Media New York 2015 CRI

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書目名稱CRISPR
副標題Methods and Protocol
編輯Magnus Lundgren,Emmanuelle Charpentier,Peter C. Fi
視頻videohttp://file.papertrans.cn/221/220552/220552.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
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: CRISPR; Methods and Protocol Magnus Lundgren,Emmanuelle Charpentier,Peter C. Fi Book 2015 Springer Science+Business Media New York 2015 CRI
描述.This volume presents a list of cutting-edge protocols for the study of CRISPR-Cas defense systems and their applications at the genomic, genetic, biochemical and structural levels.?.CRISPR: Methods and Protocols.?guides readers through techniques that have been developed specifically for the analysis of CRISPR-Cas and techniques adapted from?standard protocols of DNA, RNA and protein biology.?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,.?.CRISPR: Methods and Protocols.?provides a broad list of tools and techniques to study the interdisciplinary aspects of the prokaryotic CRISPR-Cas defense systems..
出版日期Book 2015
關(guān)鍵詞CRISPR-Cas defense systems; CRISPR-Cas9 technology; CRISPR-based genetic tools; DNA/protein; RNA/protein
版次1
doihttps://doi.org/10.1007/978-1-4939-2687-9
isbn_softcover978-1-4939-5428-5
isbn_ebook978-1-4939-2687-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2015
The information of publication is updating

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Samiran Bera,Santosh Kumar Das,Joydev Ghoshs a metal-dependent endonuclease activity. Here we describe the protocols for the analysis of nuclease activity of purified Cas1 proteins against various DNA substrates including Holliday junctions and other intermediates of DNA recombination and repair.
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In Vitro Co-reconstitution of Cas Protein Complexes,roduced as inactive inclusion bodies. Here, we present a detailed protocol for the isolation and purification of insoluble Cas proteins. Guidelines for their solubilization via co-reconstitution strategies and procedures to upscale the production of soluble multimeric Cas protein complexes are provided.
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Rapid Multiplex Creation of , Strains Capable of Interfering with Phage Infection Through CRISPR,,” can be used for very simple and rapid construction of multiple . strains capable of targeting, through CRISPR interference, any phage or plasmid of interest. Availability of such strains should allow rapid progress in the analysis of CRISPR-Cas system function against diverse mobile genetic elements.
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Electrophoretic Mobility Shift Assay of DNA and CRISPR-Cas Ribonucleoprotein Complexes,es of crRNA-Cas complexes can be quantified by calculating the dissociation constant (..). Here, we describe how two types of EMSA assays are performed using the Cascade ribonucleoprotein complex from . as an example.
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