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FACS Flourescens Activeted Cell s ortering PowerPoint Presentation
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FACS Flourescens Activeted Cell s ortering

FACS Flourescens Activeted Cell s ortering

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FACS Flourescens Activeted Cell s ortering

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  1. FACS Flourescens Activeted Cell sortering

  2. användningsområden

  3. Measurable parameters in flow cytometry • volume and morphological complexity of cells • cell pigments • DNA (cell cycle analysis, cell kinetics, proliferation etc.) • RNA • chromosome analysis and sorting (library construction, chromosome paint) • proteins • cell surface antigens (CD markers) • intracellular antigens (various cytokines, secondary mediators etc.) • nuclear antigens • enzymatic activity • pH, intracellular ionized calcium, magnesium, membrane potential • membrane fluidity • apoptosis (quantification, measurement of DNA degradation, mitochondrial membrane potential, permeability changes) • cell viability • monitoring electropermeabilization of cells • oxidative burst • characterising multi-drug resistance (MDR) in cancer cells • glutathione • various combinations (DNA / surface antigens etc.)

  4. FACS model

  5. Hydro-dynamic focusing

  6. laminärntflöde

  7. Tubulent flöde

  8. Laminärtflöde parametrar

  9. Light scattering – size of particle

  10. Scattering

  11. Forward scatter

  12. Side scatter http://www.epa.gov/owow/volunteer/proceedings/sixth/session1.html

  13. Side scatter vs Forward scatter University of Utah

  14. scatterplot

  15. Fluorimeter

  16. fluorimeteroptik Vaccine Research Center / 40 Convent Drive / Bethesda, Maryland 20892

  17. FACS diagram

  18. Fluorescens plott

  19. Lin och log

  20. Flourescens colours Fluorescein

  21. CD Cluster of diffentiation

  22. Apoptotic cells As cells die or become apoptotic the refractive index of the internal cytoplasm becomes more similar to that of the extracellular medium - this manifests itself as a reduction in forward scatter signal.  At the same time, intracellular changes and invagination of the cytoplasmic membrane lead to an increase in side (or orthogonal or 90°) scatter.  If we add a dead cell discriminatory dye we can identify cells that have become permeable.  In this way we can get low level resolution of dead and apoptotic cells.  science.cancerresearchuk.org/.../images/51998

  23. endotelceller R2= total cells R1= living cells Isolation of lymph endothelial cells (LEC) from dermal skin capillary ECs a case study with cells from one donor pre-selected by CD31 magneto bead sorting www.reliatech.de