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Titlebook: Quantitative Proteomics by Mass Spectrometry; Salvatore Sechi Book 2007 Humana Press 2007 Amino acid.Proteomics.Termination.Translation.me

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Using Stable Isotope Tagging and Mass Spectrometry to Characterize Protein Complexes and to Detect ally copurifying proteins. In this chapter, we describe a strategy for characterizing the composition of protein complexes and their dynamic changes in composition by combining affinity purification approaches with stable isotope tagging and MS. The use of software tools for statistical analysis of the data is also described.
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Stable Isotope Labeling by Amino Acids in Cell Culture for Quantitative Proteomics,rnover. SILAC allows “light” and “heavy” proteomes to be distinguished by MS while avoiding any chemical derivatization and associated purification. In this chapter, we provide detailed SILAC protocols and explain how to incorporate SILAC into any experiment.
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Proteolytic Labeling With 18O for Comparative Proteomics Studies,hed with H..O. The byproduct of the reaction is water. The use of catalytic enzyme immobilized on beads facilitates its removal and termination of the exchange. In differential proteomic studies, heavy isotope-labeled peptides are combined with peptides carrying .O for isotope ratio measurements by mass spectrometry.
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Quantitative Proteomics by Mass Spectrometry978-1-59745-255-7Series ISSN 1064-3745 Series E-ISSN 1940-6029
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