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Titlebook: New and Emerging Proteomic Techniques; Dobrin Nedelkov,Randall W. Nelson Book 2006 Humana Press 2006 Microarray.Proteomics.glycoprotein.mo

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发表于 2025-3-21 18:16:05 | 显示全部楼层 |阅读模式
书目名称New and Emerging Proteomic Techniques
编辑Dobrin Nedelkov,Randall W. Nelson
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: New and Emerging Proteomic Techniques;  Dobrin Nedelkov,Randall W. Nelson Book 2006 Humana Press 2006 Microarray.Proteomics.glycoprotein.mo
描述Leading researchers and innovators describe in step-by-step detail the latest techniques that promise to significantly impact the practice of proteomics, as well as its success in developing novel clinical agents. The methods span the entire spectrum of top-down and bottom-up approaches, including microarrays, gels, chromatography, and affinity separations, and address every aspect of the human proteome, both quantitatively and qualitatively. The techniques of protein detection utilized are diverse and range from fluorescence and resonance light scattering to surface plasmon resonance and mass spectrometry. The protocols follow the successful Methods in Molecular Biology™ series format, each offering step-by-step laboratory instructions, an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, and tips on troubleshooting and avoiding known pitfalls.
出版日期Book 2006
关键词Microarray; Proteomics; glycoprotein; molecular biology; proteins
版次1
doihttps://doi.org/10.1385/159745026X
isbn_softcover978-1-61737-615-3
isbn_ebook978-1-59745-026-3Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2006
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发表于 2025-3-21 22:09:16 | 显示全部楼层
Surface Plasmon Resonance Mass Spectrometry for Protein Analysis,odifications that go unregistered via the SPR detection can readily be assessed from the MS data. The purpose of this chapter is dissemination of the procedures and protocols for successful SPR-MS analysis. The individual steps of the complete SPR-MS process are illustrated via analysis of cardiac troponin I (cTnI).
发表于 2025-3-22 01:43:34 | 显示全部楼层
High-Throughput Affinity Mass Spectrometry,ty is normally lost in classical proteomic or immunoassay analyses. This chapter presents a step-by-step description of high-throughput AMS in the population proteomic screening of the human plasma protein cystatin C.
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Book 2006 spectrometry. The protocols follow the successful Methods in Molecular Biology™ series format, each offering step-by-step laboratory instructions, an introduction outlining the principles behind the technique, lists of the necessary equipment and reagents, and tips on troubleshooting and avoiding known pitfalls.
发表于 2025-3-22 14:15:51 | 显示全部楼层
RCA-Enhanced Protein Detection Arrays, at high sensitivity. The set of RCA reagents remains unchanged for different microarray formats and compositions, and signal readout is performed using standard fluorescent dyes and scanners. The method is sensitive enough for the most challenging applications, such as the detection of low-abundance components of human serum.
发表于 2025-3-22 18:04:08 | 显示全部楼层
Chemical Proteomics Profiling of Proteasome Activity,ease activities of the proteasome. Importantly, functional profiling is complementary to expression level profiling and is an indispensable parameter for better understanding of mechanisms underlying biological processes.
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Oligomeric States of Proteins Determined by Size-Exclusion Chromatography Coupled With Light Scattetionation step, while the responses from the three detectors are utilized to calculate the molar mass for the polypeptide portion of the native or modified protein. The amount of sugar, lipid, or detergent bound to the polypeptide chain can also be estimated from the SEC-UV/LS/RI analysis.
发表于 2025-3-23 07:36:54 | 显示全部楼层
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