2009
DOI: 10.1002/cyto.a.20706
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Spectral measurements of large particles by flow cytometry

Abstract: Flow cytometers designed to analyze large particles are enabling new applications in biology and chemistry. Similarly, flow spectroscopy approaches are extending the capabilities of the flow cytometry platform. Here, we report on the adaptation of a commercial large particle analyzer to measure fluorescence and Raman spectra of individual particles at high speeds. We modified a Union Biometrica COPAS Plus instrument to allow red excitation and optical fiber-based light collection and spectral analysis using a … Show more

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Cited by 37 publications
(35 citation statements)
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“…Investigators have tried to push the limits of detection by using bright fluorescent stains to observe particles or membrane-bound vesicles with a flow cytometer or confocal microscope (42)(43)(44). A Raman spectral flow cytometer has been used to measure particles in the far red range (45,46). Although light scatter is not the primary focus of most flow cytometry research that usually deals with surface antigens or DNA staining, it is apparent that light scatter continues to be a very interesting and useful parameter for the scientific community.…”
Section: Discussionmentioning
confidence: 99%
“…Investigators have tried to push the limits of detection by using bright fluorescent stains to observe particles or membrane-bound vesicles with a flow cytometer or confocal microscope (42)(43)(44). A Raman spectral flow cytometer has been used to measure particles in the far red range (45,46). Although light scatter is not the primary focus of most flow cytometry research that usually deals with surface antigens or DNA staining, it is apparent that light scatter continues to be a very interesting and useful parameter for the scientific community.…”
Section: Discussionmentioning
confidence: 99%
“…If an encapsulated sample contains certain fluorophores that can be excited by light of 488 nm, the emission levels can be detected for each of the objects in the encapsulated system. (Watson et al, 2009). DM: dichroic mirror; L1: 80 mm spherical lens; L2: 6 mm cylindrical lens; FC: flow cell; L3, L4: 21 mm aspherical lenses; OF: optical fiber; ND: 0.8 OD neutral density filter longitudinal axes.…”
Section: Utilization Of Micro-capsules For Next Generation Cytometricmentioning
confidence: 99%
“…Hence, it is also possible to sort micro-capsules with various magnitudes of cell growth, cell density and recombinant protein content. Watson et al, (2009) successfully adapted Union Biometrica COPAS™ Plus instrument to allow red excitation and optical fiber-based light collection and spectral analysis using a spectrograph and CCD array detector ( Figure 4B). These modifications did not compromise the ability of the instrument to resolve different sized capsules based on their extinction (EXT) and time of flight (TOF) signals.…”
Section: Utilization Of Micro-capsules For Next Generation Cytometricmentioning
confidence: 99%
“…Among these technologies are (mass) cytometry by time-of-flight (CyTOF; Watson et al 2009), comprehensive leukocyte immunophenotyping (CLIP; Biancotto et al 2011), and cytokine multiplex bead arrays (Harris and Chen 2013). These technologies are allowing investigators to explore more deeply and thoroughly the complex structure and function of the human immune system.…”
Section: Introductionmentioning
confidence: 99%