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  • 1
    Online-Ressource
    Online-Ressource
    Amsterdam, [Netherlands] :Academic Press,
    UID:
    almafu_9958129760902883
    Umfang: 1 online resource (676 p.)
    Ausgabe: First edition.
    ISBN: 9780128021958 , 0128021950 , 9780128021712 , 0128021713
    Serie: Methods in Enzymology, Volume 570
    Anmerkung: Description based upon print version of record. , Front Cover; Chemokines; Copyright; Contents; Contributors; Preface; Chapter One: Chemokine Detection Using Receptors Immobilized on an SPR Sensor Surface; 1. Surface Plasmon Resonance; 2. Chemokine Receptors: Members of the GPCR Family; 3. Chemokine Receptor Immobilization on the Sensor Chip; 4. Viral Particles as Chemokine Receptors Carriers in SPR; 4.1. Materials; 4.2. Method I: Generation of Retroviral Particles; 4.3. Method II: Generation of LVPs; 4.4. Method III: Titration of Viral Proteins; 4.5. Method IV: Determination of Chemokine Receptor Levels on the VP , 4.6. Method V: Quantitation of Receptor Number on VPs4.7. Method VI: Attachment of VPs to Biosensor Surfaces; 5. SPR-Based Applications for Chemokine Receptors; 6. Conclusions; Acknowledgments; References; Chapter Two: Study of Chemotaxis and Cell-Cell Interactions in Cancer with Microfluidic Devices; 1. Introduction; 2. Methods; 2.1. Chemotaxis in Microfluidic Chemotaxis Chamber; 2.1.1. Making Microfluidic Chemotaxis Chamber; 2.1.2. Chemotaxis Assay for Differentiated HL-60 Cells; 2.2. Gradient Switching in Microfluidic Device; 2.2.1. Making a Gradient Switching Microfluidic Device , 2.2.2. Chemotaxis Assay for Differentiated HL-60 Cells with Gradient Switch2.2.2.1. Cell Tracking and Data Analysis; 2.3. Cell-Cell Interaction in Tumor Microenvironment; 2.3.1. Creation of the Microfluidic Device; 3. Limitations; 4. Perspectives; 4.1. Shearing Force and Calculation of Chemotactic Force; 4.2. Cell Polarity Change Versus Cell Turning During a Gradient Change of Direction; 4.3. Potential Future Uses of Microfluidic Devices: Analysis of Circulating Tumor Cells; 4.4. Advantages of Using 3D Microbioreactors to Investigate Factors that Influence the Tumor Microenvironment , AcknowledgmentsReferences; Chapter Three: Generating Chemokine Analogs with Enhanced Pharmacological Properties Using Phage Display; 1. Introduction; 1.1. Chemokines in Health and Disease; 1.2. Chemokine Structure and Activity; 1.3. Applying Phage Display Technology to Chemokine Receptors; 2. Methods; 2.1. Library Design and Construction; 2.1.1. Choice of Phage Display System; 2.1.2. Introducing Library Diversity; 2.1.3. How Much Diversity Is Feasible?; 2.1.4. Partial Diversity; 2.1.5. Chemokine Walking: Exploring Diversity Step by Step; 2.1.6. Required Materials; 2.1.7. Library Construction , 2.2. Selection of Libraries on Cells2.2.1. Considerations; 2.2.2. Cell Lines; 2.2.3. Required Materials; 2.2.4. Option 1: Selection for Internalizing Ligands; 2.2.5. Option 2: Selection for High-Affinity Cell Surface Binding; 3. Limitations; 3.1. The Atypical Chemokine Receptor DARC (ACKR1); 4. Perspectives; 4.1. A Chemokine-Based HIV Prevention Strategy; 4.2. New Tools to Study CCR5 Pharmacology and Cell Biology; 4.3. An Intrakine to Protect Cells from HIV Infection and a Vaccine Adjuvant; 4.4. A Prototypic Inhibitor of CX3CR1, the Fractalkine/CX3CL1 Receptor; References , Chapter Four: Methods for the Recognition of GAG-Bound Chemokines
    Sprache: Englisch
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Online-Ressource
    Online-Ressource
    UID:
    gbv_851213138
    Umfang: 1 Online-Ressource (XXII, 632 Seiten, 20 Tafeln) , Illustrationen
    Ausgabe: First edition
    Ausgabe: Online-Ausg.
    ISBN: 9780128021712
    Serie: Methods in enzymology volume 570
    Inhalt: Front Cover -- Chemokines -- Copyright -- Contents -- Contributors -- Preface -- Chapter One: Chemokine Detection Using Receptors Immobilized on an SPR Sensor Surface -- 1. Surface Plasmon Resonance -- 2. Chemokine Receptors: Members of the GPCR Family -- 3. Chemokine Receptor Immobilization on the Sensor Chip -- 4. Viral Particles as Chemokine Receptors Carriers in SPR -- 4.1. Materials -- 4.2. Method I: Generation of Retroviral Particles -- 4.3. Method II: Generation of LVPs -- 4.4. Method III: Titration of Viral Proteins
    Inhalt: 4.5. Method IV: Determination of Chemokine Receptor Levels on the VP -- 4.6. Method V: Quantitation of Receptor Number on VPs -- 4.7. Method VI: Attachment of VPs to Biosensor Surfaces -- 5. SPR-Based Applications for Chemokine Receptors -- 6. Conclusions -- Acknowledgments -- References -- Chapter Two: Study of Chemotaxis and Cell-Cell Interactions in Cancer with Microfluidic Devices -- 1. Introduction -- 2. Methods -- 2.1. Chemotaxis in Microfluidic Chemotaxis Chamber -- 2.1.1. Making Microfluidic Chemotaxis Chamber -- 2.1.2. Chemotaxis Assay for Differentiated HL-60 Cells
    Inhalt: 2.2. Gradient Switching in Microfluidic Device -- 2.2.1. Making a Gradient Switching Microfluidic Device -- 2.2.2. Chemotaxis Assay for Differentiated HL-60 Cells with Gradient Switch -- 2.2.2.1. Cell Tracking and Data Analysis -- 2.3. Cell-Cell Interaction in Tumor Microenvironment -- 2.3.1. Creation of the Microfluidic Device -- 3. Limitations -- 4. Perspectives -- 4.1. Shearing Force and Calculation of Chemotactic Force -- 4.2. Cell Polarity Change Versus Cell Turning During a Gradient Change of Direction
    Inhalt: 4.3. Potential Future Uses of Microfluidic Devices: Analysis of Circulating Tumor Cells -- 4.4. Advantages of Using 3D Microbioreactors to Investigate Factors that Influence the Tumor Microenvironment -- Acknowledgments -- References -- Chapter Three: Generating Chemokine Analogs with Enhanced Pharmacological Properties Using Phage Display -- 1. Introduction -- 1.1. Chemokines in Health and Disease -- 1.2. Chemokine Structure and Activity -- 1.3. Applying Phage Display Technology to Chemokine Receptors -- 2. Methods -- 2.1. Library Design and Construction -- 2.1.1. Choice of Phage Display System
    Inhalt: 2.1.2. Introducing Library Diversity -- 2.1.3. How Much Diversity Is Feasible? -- 2.1.4. Partial Diversity -- 2.1.5. Chemokine Walking: Exploring Diversity Step by Step -- 2.1.6. Required Materials -- 2.1.7. Library Construction -- 2.2. Selection of Libraries on Cells -- 2.2.1. Considerations -- 2.2.2. Cell Lines -- 2.2.3. Required Materials -- 2.2.4. Option 1: Selection for Internalizing Ligands -- 2.2.5. Option 2: Selection for High-Affinity Cell Surface Binding -- 3. Limitations -- 3.1. The Atypical Chemokine Receptor DARC (ACKR1) -- 4. Perspectives
    Inhalt: 4.1. A Chemokine-Based HIV Prevention Strategy
    Anmerkung: Description based upon print version of record
    Weitere Ausg.: Erscheint auch als Druck-Ausgabe Handel, Tracy Chemokines : Elsevier Science,c2016
    Sprache: Englisch
    Fachgebiete: Biologie
    RVK:
    Schlagwort(e): Chemokine ; Biochemische Analyse ; Untersuchungsmethode ; Electronic books ; Aufsatzsammlung
    URL: Volltext  (URL des Erstveröffentlichers)
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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