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Titlebook: High Content Screening; D. Lansing Taylor,Jeffrey R. Haskins,Kenneth A. Gi Book 2006 Humana Press 2006 bioinformatics.biology.cell biology

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Characteristics and Value of Directed Algorithms in High Content Screeningvention. Thus, a suite of algorithms that are directed by an understanding of the biology being studied was developed for the optimized automated acquisition and quantitation of cellular images. Two categories of directed algorithms were developed: Developer Tools for assay development and Specific
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Automated Cell Plating and Sample Treatments for Fixed Cells in High Content Assays, are required to enable consistent, reproducible screens to be performed. We describe herein procedures and processes we have established to maximize the level of consistency of cell plating, fixation, and dye or antibody labeling, to ensure that assays which we are running on a routine basis remai
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Use of the CellCard™ System for Analyzing Multiple Cell Types in Parallel the effect of an experimental condition on a cell type of interest, but also the relative selectivity of that response across nine other cell types. In addition, this approach of cellular multiplexing is a means of miniaturization without the necessity of microfluidic devices. The standard 96-well
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Reagents to Measure and Manipulate Cell Functionsed high content screening assays. Measurement reagents include physiological indicators, immunoreagents, fluorescent analogs of macromolecules, positional biosensors, and fluorescent protein biosensors. Recent developments in reagents that manipulate specific cell functions including small inhibitor
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Fluorescent Proteins and Engineered Cell Linesnt protein sensors for expression in cellular assays requires consideration of a wide range of design factors to produce fusion proteins capable of generating informative and biologically relevant data while meeting the rigorous demands of high content screening. The target protein, fluorescent prot
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