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Titlebook: Immunoelectron Microscopy; Methods and Protocol Steven D. Schwartzbach,Tetsuaki Osafune Book 2010 Springer Science+Business Media, LLC 2010

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发表于 2025-3-21 18:44:34 | 显示全部楼层 |阅读模式
书目名称Immunoelectron Microscopy
副标题Methods and Protocol
编辑Steven D. Schwartzbach,Tetsuaki Osafune
视频videohttp://file.papertrans.cn/463/462137/462137.mp4
概述Presents a wide range of Cryo and chemical fixation methods for single cells, plant, and animal tissue.Contains Immunogold labeling methods for transmission and scanning electron microscopy.Includes c
丛书名称Methods in Molecular Biology
图书封面Titlebook: Immunoelectron Microscopy; Methods and Protocol Steven D. Schwartzbach,Tetsuaki Osafune Book 2010 Springer Science+Business Media, LLC 2010
描述Immunoelectron microscopy is a key technique that bridges the information gap between biochemistry, molecular biology, and ultrastructural studies placing macromolecular functions within a cellular context. In Immunoelectron Microscopy: Methods and Protocols, expert researchers combine the tools of the molecular biologist with those of the microscopist. From the molecular biology toolbox, this volume presents methods for antigen production by protein expression in bacterial cells,methods for epitope tagged protein expression in plant and animal cells allowing protein localization in the absence of protein specific antibodies as well as methods for the production of anti-peptide, monoclonal, and polyclonal antibodies. From the microscopy toolbox, sample preparation methods for cells, plant, and animal tissue are presented. Both cryo-methods, which have the advantage of retaining protein antigenicity at the expense of ultrastructural integrity, as well as chemical fixation methods that maintain structural integrity while sacrificing protein antigenicity have been included, with chapters examining various aspects of immunogold labeling. Written in the highly successful Methods in Mole
出版日期Book 2010
关键词Antigen; Fixation protocols; Macromolecular functions; Monoclonal Antibodies; Organelle; Pre- and post-em
版次1
doihttps://doi.org/10.1007/978-1-60761-783-9
isbn_softcover978-1-4939-5758-3
isbn_ebook978-1-60761-783-9Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media, LLC 2010
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Expression of Epitope-Tagged Proteins in Plantsurify the specific antibodies required for this method. Instead of raising antibodies against individual target proteins, the use of transgenic plants expressing epitope-tagged proteins and commercially available antibodies simplifies the subcellular localization of target proteins. In this chapter,
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Transient Expression of Epitope-Tagged Proteins in Mammalian Cellsghly specific antibodies directed against the protein of interest. Thus, only proteins for which antibodies were available could be visualized. Current technologies allow the detection of proteins for which specific antibodies are not available. This procedure involves the generation of DNA construc
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Preparation of Colloidal Gold Particles and Conjugation to Protein A, IgG, F(ab’)2, and Streptavidinells and tissues by immunoelectron microscopy (IEM). This chapter describes different methods for the preparation of colloidal gold and conjugation of colloidal gold to protein A, IgG, and streptavidin.
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Immunoelectron Microscopy of Chemically Fixed Developing Plant Embryos obstacles to ultrastructure preservation and specimen sectioning. We describe modifications of fixation and embedding procedures successfully used with microbes, protists, and mammalian tissues that have overcome these obstacles. Vacuum infiltration is used to remove intercellular air rapidly repla
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Pre-embedding Immunogold Localization of Antigens in Mammalian Brain Slicesledge about the subcellular location of antigens has formed the basis for many hypotheses regarding protein function. Many protocols have been developed since the introduction of colloidal gold to immunocytochemistry. The two most widely used techniques, however, are based on transmission electron m
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