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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Proteomics. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (445 pages)
    Edition: 1st ed.
    ISBN: 9780080569154
    Series Statement: Issn Series
    DDC: 547.7/5
    Language: English
    Note: Cover -- Advances in Protein Chemistry -- Copyright -- Contents -- Proteomics in the Postgenomic Age -- I. Introduction -- II. Deciphering the Genome -- III. Gene Expression Profiles -- IV. A Niche for Proteomics -- V. The Proteome: Greater than the Sum of its Parts -- VI. Biological and Clinical Applications -- VII. Proteomics Meets Cell Biology -- VIII. Summary -- References -- The Tools of Proteomics -- I. Introduction -- II. Ionization Methods -- III. Mass Analyzers -- IV. Sample Fractionation -- V. Software Tools -- VI. Conclusions -- References -- Proteomic Analysis by Two-Dimensional Polyacrylamide Gel Electrophoresis -- I. Introduction -- II. Historical Development of 2D-PAGE -- III. Limitations and Advances -- IV. Protein Visualization Methods -- V. Proteome Application of 2D-PAGE -- VI. The Future -- Acknowledgments -- References -- High-Performance Separations and Mass Spectrometric Methods for High-Throughput Proteomics Using Accurate Mass Tags -- I. Introduction -- II. Proteome Measurement Technology and Applications -- III. Technology Advances for Expanding Proteome Coverage -- Acknowledgments -- References -- Current Strategies for Quantitative Proteomics -- I. Introduction -- II. Quantitative Two-Dimensional Polyacrylamide Gel Electrophoresis -- III. Metabolic Labeling Applications for Quantitative Proteomics -- IV. Chemical Modification Strategies for Quantitative Proteome Measurements -- V. Conclusions -- Acknowledgments -- References -- Proteome Analysis of Posttranslational Modifications -- I. Introduction -- II. Phosphorylation -- III. Mass Spectral Identification of Phosphopeptides -- IV. Glycosylation -- V. Conclusions -- Acknowledgments -- References -- Mapping Protein Modifications with Liquid Chromatography-Mass Spectrometry and the SALSA Algorithm -- I. Introduction -- II. MS-MS Fragmentation of Modified Peptides. , III. SALSA: A Pattern Recognition Algorithm to Identify MS-MS Spectra for Modified Peptides -- IV. Mapping Protein Modifications with SALSA -- V. Comparison of SALSA with Other Software for Analysis of MS-MS Data -- Acknowledgments -- References -- Emerging Role of Mass Spectrometry in Structural and Functional Proteomics -- I. Introduction -- II. Application of ESI-MS in Structural and Functional Proteomics -- III. Future Directions -- Acknowledgments -- References -- Application of Separation Technologies to Proteomics Research -- I. Introduction -- II. What Is Proteomics? -- III. What Needs to Be Separated? -- IV. Slab Gel Electophoresis, High-Performance Liquid Chromatography, or Capillary Electrophoresis? -- V. Multidimensional Separations of Proteins -- VI. On-Column HPLC and CE Protein Concentration -- VII. Detection -- VIII. Proteome Quantitation Strategies -- IX. Conclusion -- Acknowledgments -- References -- Proteomics of Membrane Proteins -- I. Introduction -- II. Techniques -- III. Applications: The Thylakoid Membrane Proteome -- IV. Conclusions -- Acknowledgments -- References -- Proteomics in Drug Discovery -- I. Introduction -- II. The Complexity of Proteomic Analysis in Drug Discovery -- III. Proteomic Strategies in Drug Discovery -- IV. Quantification in Proteomic Studies -- V. Applications -- VI. Functional Proteomics Approach -- VII. Future Trends in Proteomics -- References -- From Clone to Crystal: Maximizing the Amount of Protein Samples for Structure Determination -- I. Introduction -- II. Technology Drives the Process -- III. From Sequence to Solubility: The First Step -- IV. Alternative Expression Systems -- V. Screening for the Most Soluble Ortholog -- VI. Cofactor Screens -- VII. Solubility Screens -- VIII. From Solubility to Structure: The Second Step -- IX. Conclusions -- References -- Proteomics and Bioinformatics. , I. Introduction -- II. Bioinformatics Tools -- III. Proteomics Tools -- IV. Database Integration -- V. Conclusions -- Acknowledgments -- References -- AUTHOR INDEX -- SUBJECT INDEX.
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  • 2
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1693-1697 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Fibers of organic polymers (polystyrene, cellulose acetate, and polypropylene) were formed by the rapid expansion of supercritical fluid solutions through a small diameter nozzle to ambient temperature and pressure. Solutions were prepared either by dissolving the polymer directly in room temperature pentane, or in an autoclave at elevated temperatures and pressures for less soluble polymers. The fibers were collected on substrates mounted in the expansion jet. The diameters of the fibers formed (typically 1-5 μm) were much smaller than the opening of the nozzle, although fiber diameter was observed to generally increase with nozzle diameter. The aspect ratios of the fibers, produced by this process were on the order of 103 or larger. Optimum conditions for fiber formation occurred at fluid expansion temperatures near the melting point of the polymer, with particle formation mechanisms favored at higher and lower temperatures.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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