Titlebook: Quantitative Proteomics by Mass Spectrometry; Salvatore Sechi Book 2016Latest edition Springer Science+Business Media New York 2016 proteo

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Mass Spectrometry-Based Quantitative O-GlcNAcomic Analysis,nine residues is critical in many cellular processes, contributing to multiple physiological and pathological events. The term “O-GlcNAcome” refers to not only the complete set of proteins that undergo O-GlcNAcylation but also the O-GlcNAc status at individual residues, as well as the dynamics of O-

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Isolating and Quantifying Plasma HDL Proteins by Sequential Density Gradient Ultracentrifugation annt of many proteins in complex mixtures. Its application to the relative quantification of proteins in high-density lipoproteins (HDL) that have been purified from human plasma has revealed potential mechanisms to explain the atheroprotective effects of HDL. We describe a moderate throughput method

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High-Throughput Quantitative Proteomics Enabled by Mass Defect-Based 12-Plex DiLeu Isobaric Tags,owever, widespread use of the approach for large-scale proteomics applications has been limited by the high cost of commercial isobaric tags. To address this, we have developed our own .,.-dimethyl leucine (DiLeu) multiplex isobaric tags as a cost-effective alternative that can be synthesized with e

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Multiple and Selective Reaction Monitoring Using Triple Quadrupole Mass Spectrometer: Preclinical Live peptides for the detection and quantitation of a protein. Compared to traditional ELISA, MRM assays have a number of advantages including ease in multiplexing several proteins in the same assay and independence from the necessity for high-quality, expensive, and at times unreliable antibodies. F