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Titlebook: Capillary Electrophoresis of Carbohydrates; Pierre Thibault,Susumu Honda Book 2003 Humana Press 2003 carbohydrate chemistry

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發(fā)表于 2025-3-21 18:42:37 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱Capillary Electrophoresis of Carbohydrates
編輯Pierre Thibault,Susumu Honda
視頻videohttp://file.papertrans.cn/222/221392/221392.mp4
概述Includes supplementary material:
叢書(shū)名稱Methods in Molecular Biology
圖書(shū)封面Titlebook: Capillary Electrophoresis of Carbohydrates;  Pierre Thibault,Susumu Honda Book 2003 Humana Press 2003 carbohydrate chemistry
描述Recent developments in high-resolution separation techniques based on capillary-scale chromatography and electrophoresis have transformed the analysis of free and conjugated mono- and oligosaccharides. In Capillary Electrophoresis of Carbohydrates, hands-on experts describe cutting-edge techniques in capillary electrophoresis (CE) for the analysis of complex carbohydrates. Written in step-by-step detail to ensure successful experimental results, these readily reproducible protocols provide methods for sample preparation and analysis of mono- and oligosaccharides, glycoproteins, and glycoconjugates. Different CE separation formats, including capillary zone electrophoresis (CZE), capillary isoelectric focusing (CIEF), capillary isotachophoresis (CITP), capillary gel electrophoresis (CGE), and micellar electrokinetic chromatography (MEKC), are presented for different types of applications, such as the analysis of glycoforms, the separation of enantiomers, and the resolution of oligosaccharides. The separation of native derivatized carbohydrates is presented using UV, fluorescence, and mass spectrometric detection. Two other applications demonstrate the use of CE as an assay method for
出版日期Book 2003
關(guān)鍵詞carbohydrate chemistry
版次1
doihttps://doi.org/10.1385/1592592945
isbn_softcover978-1-61737-206-3
isbn_ebook978-1-59259-294-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2003
The information of publication is updating

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Newton’s Sensorium: Anatomy of a Conceptgroups linked to each other. In reducing monosaccharides the hemiacetal group is at the reducing ends in addition to these polyhydroxylated basal structures. There are other series of monosaccharides with the ketal or carboxyl group instead of or in addition to the hemiacetal group. Substitution of
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Misunderstanding Art: The Myth of Enrichment thought to be involved in the regulation of the physiological functions of these proteins (.). Although the polysaccharide backbone of GAGs is a linear polymer composed of alternating amino sugar and hexuronic acid residues, this simple repeat structure acquires a considerable degree of variability
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‘The Murderousness and Gadgetry of this Age’uctures and properties. All carbohydrates contain hydroxyl group and most of them in addition have a characteristic functional group, such as the hemiacetal (aldoses), keto (ketoses), and carboxyl (aldonic and saccharic acids) groups. There are also compounds having two or more of such functional gr
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Digitally Assisted Self-Organization,ssible. A homopolymer of glucose with a glycosidic bond may assume its stere-ochemical configuration at either the α or β position. Glucose units could be joined through 1,2; 1,3; 1,4; or 1,6 linkages in linear sequence or extended through different linkages, which eventually could lead to a two- or
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