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Titlebook: Single Cell Protein Analysis; Methods and Protocol Anup K. Singh,Aarthi Chandrasekaran Book 2015 Springer Science+Business Media New York 2

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发表于 2025-3-21 19:49:46 | 显示全部楼层 |阅读模式
书目名称Single Cell Protein Analysis
副标题Methods and Protocol
编辑Anup K. Singh,Aarthi Chandrasekaran
视频videohttp://file.papertrans.cn/868/867787/867787.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.Includes supplementary materia
丛书名称Methods in Molecular Biology
图书封面Titlebook: Single Cell Protein Analysis; Methods and Protocol Anup K. Singh,Aarthi Chandrasekaran Book 2015 Springer Science+Business Media New York 2
描述.This volume highlights recent developments in flow cytometry, affinity assays, imaging, mass spectrometry, microfluidics and other technologies that enable analysis of proteins at the single cell level. The book also includes chapters covering a suite of biochemical and biophysical methods capable of making an entire gamut of proteomic measurements, including analysis of protein abundance or expression, protein interaction networks, post-translational modifications, translocation and enzymatic activity. 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 thorough, .Single Cell Protein Analysis: Methods and Protocols. is useful to researchers and students in biological and biomedical sciences who have an interest in proteomic measurements in cells. .
出版日期Book 2015
关键词Cell Signaling; Flow Cytometry; Gel Electrophoresis; Heterogeneous; Immunoassays; Mass Spectrometry; Micro
版次1
doihttps://doi.org/10.1007/978-1-4939-2987-0
isbn_softcover978-1-4939-4943-4
isbn_ebook978-1-4939-2987-0Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2015
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Imaging and Mapping of Tissue Constituents at the Single-Cell Level Using MALDI MSI and Quantitativar-resolution constituent maps. For the first time, laser scanning cytometry (LSC) and matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) are combined for the analysis of tissue sections. The utility of the marriage of these techniques is demonstrated by analyzing mous
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SPLIFF: A Single-Cell Method to Map Protein-Protein Interactions in Time and Space,bsequently cleaved from the C-terminus of C. and degraded whereas the red-fluorescent mCherry stays attached to the C.-fusion protein. We first implemented this method in the model yeast .. One fusion protein is expressed in cells of the a-mating type and the complementary fusion protein in cells of
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1064-3745 gle Cell Protein Analysis: Methods and Protocols. is useful to researchers and students in biological and biomedical sciences who have an interest in proteomic measurements in cells. .978-1-4939-4943-4978-1-4939-2987-0Series ISSN 1064-3745 Series E-ISSN 1940-6029
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Catherine M. Rawlins,Joseph P. Salisbury,Daniel R. Feldman,Sinan Isim,Nathalie Y. R. Agar,Ed Luther,änden erheblich verstärkt werden (Resonanz, Resonanzboden des Klaviers). Dieses Mitklingen kann auch dann ausgelöst werden, wenn die Schwingungen in eine am unteren Ende verschlossene Röhre hineinfallen. Hier werden dann durch das Zusammenwirken (Interferenz) der zurückgeworfenen Wellen mit den neue
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Matthias Blazek,Günter Roth,Roland Zengerle,Matthias Meieränden erheblich verstärkt werden (Resonanz, Resonanzboden des Klaviers). Dieses Mitklingen kann auch dann ausgelöst werden, wenn die Schwingungen in eine am unteren Ende verschlossene Röhre hineinfallen. Hier werden dann durch das Zusammenwirken (Interferenz) der zurückgeworfenen Wellen mit den neue
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