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Titlebook: Oligonucleotide-Based Therapies; Methods and Protocol Olof Gissberg,Rula Zain,Karin E. Lundin Book 2019 Springer Science+Business Media, LL

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發(fā)表于 2025-3-21 18:59:31 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Oligonucleotide-Based Therapies
副標(biāo)題Methods and Protocol
編輯Olof Gissberg,Rula Zain,Karin E. Lundin
視頻videohttp://file.papertrans.cn/701/700863/700863.mp4
概述Includes cutting-edge techniques.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Oligonucleotide-Based Therapies; Methods and Protocol Olof Gissberg,Rula Zain,Karin E. Lundin Book 2019 Springer Science+Business Media, LL
描述This book provides a collection of comprehensive, up-to-date, and broadly applicable guides to the research and development fields of oligonucleotide (ON) therapeutics. Covering topics from the study of antisense and anti-gene effects to oligonucleotides in the context of drug discovery and development, the volume explores a wide-ranging and useful spectrum of methods and protocols needed to take full advantage of therapeutic applications involving ONs. Written for the highly successful .Methods in Molecular Biology. series, 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 practical, .Oligonucleotide-Based Therapies: Methods and Protocols. aims to be a great aid in the laboratory as well as an ideal reference guide when designing antisense and anti-gene oligonucleotides for therapeutic applications..
出版日期Book 2019
關(guān)鍵詞Drug discovery and development; Targeting strategies; Antisense; Therapeutic applications; Anti-gene oli
版次1
doihttps://doi.org/10.1007/978-1-4939-9670-4
isbn_softcover978-1-4939-9672-8
isbn_ebook978-1-4939-9670-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC, part of Springer Nature 2019
The information of publication is updating

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Tissue-Specific Delivery of Oligonucleotidesl to the current CRISPR-Cas9 system offering gene editing at the genomic level, oligonucleotides, in addition to their biological functions in storing and conveying genetic information, provide the most prominent solutions to targeted gene therapies. Nonetheless, looking into the future of curing ca
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Designing siRNA and Evaluating Its Effect on RNA Targets Using qPCR and Western Blotunderstanding of gene function. Carefully designed siRNAs can considerably improve siRNA specificity leading to more accurate and efficient gene silencing. Evaluation of gene knockdown is vital for optimization of siRNA efficacy. Here we describe the fundamental principles of siRNA design and strate
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Assessing Oligonucleotide Binding to Double-Stranded DNAc approaches. Several methods can be used to evaluate ONs effect and binding capacity to their target sequence. Here we describe some of the methods, which have been frequently used for assessing ONs binding to dsDNA.
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Modeling and Simulation of Oligonucleotide Hybrids: Outlining a Strategyres of biomolecules. Effects of chemical modifications and of the environment such as sequence, solvent, and ionic strength can explicitly be taken into account. Molecular simulation techniques can also provide insight in change in binding affinity, in protonation (p. shift) and tautomeric propensit
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Attachment of Peptides to Oligonucleotides on Solid Support Using Copper(I)-Catalyzed Huisgen 1,3-Di ONs with cell penetrating, homing or endosomal escape peptides can enhance specificity and/or uptake efficiencies. We describe here a general procedure for the preparation of peptide–oligonucleotide conjugates (POCs) on solid support utilizing a novel activated alkyne containing linker which enhanc
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Characterizing Oligonucleotide Uptake in Cultured Cells: A Case Study Using AS1411 Aptamer of the target. The therapeutic potential of oligonucleotides targeted to intracellular molecules will depend largely on their ability to be taken up by the cells of interest, as well as their subsequent subcellular distribution. Here we describe methods to characterize the extent and mechanism of c
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