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Titlebook: Macro-Glycoligands; Methods and Protocol Xue-Long Sun Book 2016 Springer Science+Business Media New York 2016 Glycopolymer-nanoparticle con

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發(fā)表于 2025-3-21 17:49:02 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Macro-Glycoligands
副標(biāo)題Methods and Protocol
編輯Xue-Long Sun
視頻videohttp://file.papertrans.cn/621/620965/620965.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(chēng)Methods in Molecular Biology
圖書(shū)封面Titlebook: Macro-Glycoligands; Methods and Protocol Xue-Long Sun Book 2016 Springer Science+Business Media New York 2016 Glycopolymer-nanoparticle con
描述.This volume details methods and protocols for the synthesis and characterization of glycopolymers and their biomedical applications. Chapters are divided into three parts covering synthesis and characterization of glycopolymers; glycopolymer-nanoparticle conjugates; and surface immobilized glycopolymers. ?Written for the .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, .Macro-Glycoligands: Methods and Protocols. aims to ensure successful results in the further study of this vital field..
出版日期Book 2016
關(guān)鍵詞Glycopolymer-nanoparticle conjugates; carbohydrate chemistry; carbohydrate recognition; glycans; glycobi
版次1
doihttps://doi.org/10.1007/978-1-4939-3130-9
isbn_softcover978-1-4939-4948-9
isbn_ebook978-1-4939-3130-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2016
The information of publication is updating

書(shū)目名稱(chēng)Macro-Glycoligands影響因子(影響力)




書(shū)目名稱(chēng)Macro-Glycoligands影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Macro-Glycoligands網(wǎng)絡(luò)公開(kāi)度




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書(shū)目名稱(chēng)Macro-Glycoligands被引頻次




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Glycopolymers Prepared by Ring-Opening Metathesis Polymerization Followed by Glycoconjugation Using olymerization is followed by attachment of a linker and subsequent glycoconjugation via a triazole-forming azide-alkyne click reaction. The use of a protected amine-terminating agent allows for the attachment of a probe molecule such as a fluorescein dye. The syntheses of a neutral galactopolymer as
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Protecting-Group-Free Synthesis of Glycopolymers and Their Binding Assay with Lectin and Influenza Vbe a facile protecting-group-free synthetic approach to glycopolymers bearing oligosaccharides from free saccharides by direct azidation and click chemistry methods, followed by reversible addition-fragmentation chain transfer polymerization. This method can be applied not only to mono- and disaccha
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Carbohydrate-Based Initiators for the Cationic Ring-Opening Polymerization of 2-Ethyl-2-Oxazolinebiomedical applications according to their specific needs. This contribution describes the detailed methodology to functionalize poly(2-ethyl-2-oxazoline), a polymer with properties very similar to polyethylene glycol, in a stereo-selective manner with a range of carbohydrates that can serve as biol
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Heterofunctional Glycopolypeptides by Combination of Thiol-Ene Chemistry and NCA Polymerizationonalization of polypeptides with suitable functional groups. Here we present a method for the in-situ functionalization and (co-) polymerization of allylglycine .-carboxyanhydride in a facile one-pot procedure, combining radical thiol-ene photochemistry and nucleophilic ring-opening polymerization t
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Galactosylated Polymer Nano-objects by Polymerization-Induced Self-Assembly, Potential Drug Nanocarrization-induced self-assembly, especially RAFT aqueous dispersion polymerization is a unique method to prepare such polymer nanostructures, as it enables the preparation of very-well-defined morphologies at very high concentrations. Here we describe the implementation of PISA to the synthesis of gal
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Surface Modification of Polydivinylbenzene Microspheres with a Fluorinated Glycopolymer Using Thiol-ified with polypentafluorostyrene chains utilizing surface-initiated atom transfer radical polymerization techniques. The hydrophobic fluoropolymer-coated microsphere was then converted to a hydrophilic biopolymer by performing thiol-halogen click chemistry between polypentafluorostyrene and 1-thio-
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