Flow cytometry basics for the non-expert /

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Bibliographic Details
Author / Creator:Goetz, Christine, author.
Imprint:Cham : Springer, 2018.
Description:1 online resource (229 pages)
Language:English
Series:Techniques in Life Science and Biomedicine for the Non-Expert
Techniques in life science and biomedicine for the non-expert.
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11737611
Hidden Bibliographic Details
Other authors / contributors:Hammerbeck, Christopher.
Bonnevier, Jody.
ISBN:9783319980713
3319980718
9783319980706
331998070X
Digital file characteristics:text file PDF
Notes:1 Antibody Development for Flow Cytometry.
Print version record.
Summary:Flow cytometry allows for the measurement of different aspects of a cell or particles in real time. Applications include quantifying various types of T cells to determine the presence of various immune disorders, such as whether HIV has progressed to AIDS, studying the dynamics of immune signaling in cells to detect the suppression of normal immune function, and analyzing biopsy specimens for tumors, to aid in cancer diagnosis and prognosis. In addition to simplifying the technique and using vocabulary accessible to those not trained in cell biology and immunology, the book includes the following 4 unqiue features: 1) Tips on how to set up an experiment for flow cytometry optimially 2) An expanded data set of flow staining including multiparameter flow cytometry 3) Detailed staining protocols for flow cytometry (ex. protocols optimized for transcription factors, secreted cytokines, phospho-antibodies, and surface antigens) 4) Section devoted to antibody development and conjugation.
Other form:Print version: Goetz, Christine. Flow Cytometry Basics for the Non-Expert. Cham : Springer, ©2018 9783319980706
Standard no.:10.1007/978-3-319-98071-3

MARC

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505 0 |a Intro; Preface; Acknowledgments; Contents; About the Book; Chapter 1: Flow Cytometry: Definition, History, and Uses in Biological Research; 1 Components of Flow Cytometry; 2 Definition of Flow Cytometry; 3 History of Flow Cytometry; 3.1 Cellular Impedance and the Coulter Principle; 3.2 Fluorescence-Based Flow Cytometers; 3.3 Monoclonal and Polyclonal Antibodies; 3.4 Fluorescent Molecules; 3.5 Fluorescence Activated Cell Sorting (FACS); 4 Modern Flow Cytometers; 4.1 Fluidic-Based Flow Cytometers; 4.2 Acoustic-Based Flow Cytometers; 4.3 Mass Cytometers (CyTOF); References. 
505 8 |a Chapter 2: Physics of a Flow Cytometer1 Components of Fluidic-Based Flow Cytometers; 1.1 Fluidics; 1.2 Optics; 1.3 Electronics; 2 Putting It All Together; 3 Materials; 3.1 Flow Antibodies; 3.2 Cell Activation Reagents; 3.3 Cell Purification Kits; 3.4 Staining Buffers/Fc Block Reagents; References; Chapter 3: The Language of Flow Cytometry and Experimental Setup; 1 Flow Data Plots and Gating; 1.1 Flow Data Plots; 1.2 Gating; 2 Mean Fluorescence Intensity (MFI) and Biexponential vs. Logarithmic Scaling; 2.1 Mean Fluorescence Intensity (MFI); 2.2 Logarithmic vs. Biexponential Scaling. 
505 8 |a 3 Forward Scatter (FSC)/Side Scatter (SSC) and Doublet Exclusion3.1 FSC/SSC; 3.2 Doublet Exclusion; 4 CS & T and Basic Experimental Setup; 4.1 CS 4.2 Basic Experimental Setup; 4.2.1 Experimental/Flow Panel Design; 4.2.2 Surface and Intracellular Staining on iTregs; 4.2.3 Experimental Setup on the Fortessa; 4.2.4 Sample Acquisition and Analysis; 5 Basic Concepts of Compensation; 6 Materials; 6.1 Flow Antibodies; 6.2 Cell Activation Reagents; 6.3 Cell Purification Kits; 6.4 Staining Buffers/Fc Block Reagents; References; Chapter 4: Fluorochrome Choices for Flow Cytometry. 
505 8 |a 1 Fluorochromes and Their Pros and Cons2 Spectrum Viewers and How to Use Them; 3 Fluorochrome Combinations to Use/Avoid Together; 4 Laser Strength on the Fortessa vs. the Calibur; 5 High- vs. Low-Density Cell Markers and Fluorochrome Choice; 6 Materials; 6.1 Flow Antibodies; 6.2 Staining Buffers/Fc Block Reagents; References; Chapter 5: Using the Process of Compensation to Prevent False Positive Data Caused by Fluorescence Spillover: A Practical Example; 1 Compensation: A Practical Example; 2 Manual Compensation by Comparing the Median Fluorescence Intensity of Cell Populations. 
505 8 |a 3 Considerations When Performing Compensation3.1 Using the Same Compensation Settings for Multiple Experiments; 3.2 Dimming of Fluorochromes as a Result of Compensation; 3.3 Consider the Number of Overlapping Fluorochromes; 3.4 Consider If Compensation Is Necessary; 3.5 Consider If Fluorochromes with High Spectral Overlap Can Be Separated on Two Different Cell Types; 3.6 Using Cells as Single-Stain Controls vs. Beads; 4 Materials; 4.1 Flow Antibodies; 4.2 Staining Buffers/Fc Block Reagents; References; Chapter 6: Primary and Secondary Antibodies and Flow Cytometry Controls. 
500 |a 1 Antibody Development for Flow Cytometry. 
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