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Basic Principles, Instrumentation, and Practices

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Presentation on theme: "Basic Principles, Instrumentation, and Practices"— Presentation transcript:

1 Basic Principles, Instrumentation, and Practices
Flow Cytometry Basic Principles, Instrumentation, and Practices

2 Introduction/Basic Facts
Laser-optics-computer based technology for measuring the characteristics of biological particles Bioparticles can be whole cells or prepared cellular constituents Uses a one particle at a time approach for analysis rather than measuring a bulk property Measures the light scattering and fluorescence properties of particles

3 Biological Cell 5-20 µm in diameter

4 Cell Labeling Techniques
Antibodies Conjugated to Fluorochromes FITC, Phycoerythrin, proprietary Cytoplasmic Dyes/Stains Permeant, nonpermeant Nuclear stains Membrane dyes

5 Most Common Cell Labeling
Single Antibody Dual Antibody Internal

6 Flow Cytometry Applications
Detection of Intracellular Cytokine Production Detection of Intracellular/intranuclear antigens Estimation of cell viability Cell transmembrane potential measurements Measurement of oxidative metabolism Measurement of environmental particulate uptake Detection of intracellular cyclins

7 List of Flow Cytometry Applications
Pharmacokinetic monitoring Quantitation of proteins inserted into membranes Quantitation of electropermeabilization Cell cycle analysis Analysis of apoptosis Cell Sorting Chromosome sorting Up to 7 fluorochrome analysis

8 1969 Los Almos Labs created the first flow cytometer
Normally have a dedicated operator USF researchers have access to the Moffitt Core Flow Cytometry Facility

9 Flow Cytometer Block Diagram

10 Spectral Overlap

11 Compensating for Spectral Overlap

12 Control Samples Compensation – for 2 or more colors Negative
Unlabeled cell – zero reference point Isotype control – nonspecific binding Positive – make sure that labeled antibody is functional

13 Examples of Flow Cytometric Analysis
One parameter FSC analysis for cell size One parameter FL1 analysis for drug uptake Two parameter fluorescence analysis for dual labeled cells Cell Sorting

14 One Parameter FSC Analysis

15 One Parameter FL1 Analysis

16 One Parameter FL1 Analysis

17 Fluorescence Two Color Analysis
Unfused Fused

18 Fluorescence Two Color Analysis

19 Cell Sorting Filters/ detectors +/- V +/- V


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