Measuring biological responses with automated microscopy

Author(s)

• Inglese, James

Bibliographic Information

Measuring biological responses with automated microscopy

edited by James Inglese

（Methods in enzymology / editors in chief, Sidney P. Colowick, Nathan O. Kaplan, v. 414）

Academic Press, c2006

Note

Includes bibliographical references and indexes

Description and Table of Contents

Description

The critically acclaimed laboratory standard for more than forty years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with more than 300 volumes (all of them still in print), the series contains much material still relevant today-truly an essential publication for researchers in all fields of life sciences.

Table of Contents

[1]: Dynamic Green Fluorescent Protein Sensors for High-Content Analysis of the Cell Cycle [2]: High-Content Fluorescence-Based Screening for Epigenetic Modulators [3]: Development of Assays for Nuclear Receptor Modulators Using Fluorescently Tagged Proteins [4]: The Ligand-Independent Translocation Assay: An Enabling Technology for Screening Orphan G Protein-Coupled Receptors by Arrestin Recruitment [5]: High-Content Screening of Known G Protein-Coupled Receptors by Arrestin Translocation [6]: Cell Imaging Assays for G Protein-Coupled Receptor Internalization: Application to High-Throughput Screening [7]: High-Throughput Confocal Microscopy for ss-Arrestin-Green Fluorescent Protein Translocation G Protein-Coupled Receptor Assays Using the Evotec Opera [8]: G Protein-Coupled Receptor Internalization Assays in the High-Content Screening Format [9]: Screening for Activators of the Wingless Type/Frizzled Pathway by Automated Fluorescent Microscopy [10]: A Live Cell, Image-Based Approach to Understanding the Enzymology and Pharmacology of 2-Bromopalmitate and Palmitoylation [11]: High-Resolution, High-Throughput Microscopy Analyses of Nuclear Receptor and Coregulator Function [12]: Tracking Individual Proteins in Living Cells Using Single Quantum Dot Imaging [13]: Development and Application of Automatic High-Resolution Light Microscopy for Cell-Based Screens [14]: Adenoviral Sensors for High-Content Cellular Analysis [15]: Cell-Based Assays Using Primary Endothelial Cells to Study Multiple Steps in Inflammation [16]: Development and Implementation of Multiplexed Cell-Based Imaging Assays [17]: High-Throughput Screening for Modulators of Stem Cell Differentiation [18]: High-Content Kinetic Calcium Imaging in Drug-Sensitive and Drug-Resistant Human Breast Cancer Cells [19]: Measurement and Analysis of Calcium Signaling in Heterogeneous Cell Cultures [20]: Multiplex Analysis of Inflammatory Signaling Pathways Using a High-Content Imaging System [21]: Generation and Characterization of a Stable MK2-EGFP Cell Line and Subsequent Development of a High-Content Imaging Assay on the Cellomics ArrayScan Platform to Screen for p38 Mitogen-Activated Protein Kinase Inhibitors [22]: Development and Implementation of Three Mitogen-Activated Protein Kinase (MAPK) Signaling Pathway Imaging Assays to Provide MAPK Module Selectivity Profiling for Kinase Inhibitors: MK2-EGFP Translocation, c-Jun, and ERK Activation [23]: Assay Development and Case History of a 32K-Biased Library High-Content MK2-EGFP Translocation Screen to Identify p38 Mitogen-Activated Protein Kinase Inhibitors on the ArrayScan 3.1 Imaging Platform [24]: Compound Classification Using Image-Based Cellular Phenotypes [25]: High-Content Screening: Emerging Hardware and Software Technologies [26]: An Infrastructure for High-Throughput Microscopy: Instrumentation, Informatics, and Integration [27]: Protein Translocation Assays: Key Tools for Accessing New Biological Information with High-Throughput Microscopy [28]: High-Content Screening of Functional Genomic Libraries [29]: Fluorescent Protein-Based Cellular Assays Analyzed by Laser-Scanning Microplate Cytometry in 1536-Well Plate Format [30]: High-Throughput Measurements of Biochemical Responses Using the Plate::Vision Multimode 96 Minilens Array Reader [31]: Systems Cell Biology Based on High-Content Screening [32]: Digital Autofocus Methods for Automated Microscopy [33]: Fluorescence Lifetime Imaging Microscopy: Two-Dimensional Distribution Measurement of Fluorescence Lifetime Author Index Subject Index

by "Nielsen BookData"

Details

• NCID: BA78910492
• ISBN:
  • 0121828190
• Country Code: ne
• Title Language Code: eng
• Text Language Code: eng
• Place of Publication: Amsterdam ; San Diego, Calif. ; Tokyo
• Pages/Volumes: xliv, 691 p.
• Size: 24 cm
• Subject Headings:
  • MESH : Microscopy
  • MESH : Tumor Markers, Biological
• Parent Bibliography ID:
  • BA00197543