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flow cytometry data acquisition system azurite  (DarklingX LLC)

 
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    DarklingX LLC flow cytometry data acquisition system azurite
    Flow Cytometry Data Acquisition System Azurite, supplied by DarklingX LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/flow cytometry data acquisition system azurite/product/DarklingX LLC
    Average 90 stars, based on 1 article reviews
    flow cytometry data acquisition system azurite - by Bioz Stars, 2026-03
    90/100 stars

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    Johns Hopkins HealthCare flow cytometry data acquisition and analysis
    ZnT8-specific surface labeling of live INS-1E cells. A, representative confocal images of immunofluorescence staining of WT or ZnT8 KO cells using a proteoliposome- or liposome-immunized serum as indicated. Scale bar, 20 μm. B, histograms of surface immunofluorescence intensities measured in >10,000 WT INS-1E cells that were stained by a proteoliposome- and liposome-immunized serum as indicated. The solid lines are least square fits to a Lorentzian distribution. Arrows indicate serum titrations with increasing concentrations. C, identical experiments in B except that ZnT8 KO INS-1E cells were used. D, saturation of surface immunofluorescence staining with increasing serum concentrations. The concentration-intensity relationships were plotted using flow <t>cytometry</t> data in B and C (mean intensity ± S.E.). The solid lines are hyperbolic fits of concentration-dependent surface staining with a proteoliposome- or liposome-immunized serum as indicated.
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    DarklingX LLC flow cytometry data acquisition system azurite
    ZnT8-specific surface labeling of live INS-1E cells. A, representative confocal images of immunofluorescence staining of WT or ZnT8 KO cells using a proteoliposome- or liposome-immunized serum as indicated. Scale bar, 20 μm. B, histograms of surface immunofluorescence intensities measured in >10,000 WT INS-1E cells that were stained by a proteoliposome- and liposome-immunized serum as indicated. The solid lines are least square fits to a Lorentzian distribution. Arrows indicate serum titrations with increasing concentrations. C, identical experiments in B except that ZnT8 KO INS-1E cells were used. D, saturation of surface immunofluorescence staining with increasing serum concentrations. The concentration-intensity relationships were plotted using flow <t>cytometry</t> data in B and C (mean intensity ± S.E.). The solid lines are hyperbolic fits of concentration-dependent surface staining with a proteoliposome- or liposome-immunized serum as indicated.
    Flow Cytometry Data Acquisition System Azurite, supplied by DarklingX LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/flow cytometry data acquisition system azurite/product/DarklingX LLC
    Average 90 stars, based on 1 article reviews
    flow cytometry data acquisition system azurite - by Bioz Stars, 2026-03
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    DarklingX LLC flow cytometry data acquisition system
    ZnT8-specific surface labeling of live INS-1E cells. A, representative confocal images of immunofluorescence staining of WT or ZnT8 KO cells using a proteoliposome- or liposome-immunized serum as indicated. Scale bar, 20 μm. B, histograms of surface immunofluorescence intensities measured in >10,000 WT INS-1E cells that were stained by a proteoliposome- and liposome-immunized serum as indicated. The solid lines are least square fits to a Lorentzian distribution. Arrows indicate serum titrations with increasing concentrations. C, identical experiments in B except that ZnT8 KO INS-1E cells were used. D, saturation of surface immunofluorescence staining with increasing serum concentrations. The concentration-intensity relationships were plotted using flow <t>cytometry</t> data in B and C (mean intensity ± S.E.). The solid lines are hyperbolic fits of concentration-dependent surface staining with a proteoliposome- or liposome-immunized serum as indicated.
    Flow Cytometry Data Acquisition System, supplied by DarklingX LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/flow cytometry data acquisition system/product/DarklingX LLC
    Average 90 stars, based on 1 article reviews
    flow cytometry data acquisition system - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    Image Search Results


    ZnT8-specific surface labeling of live INS-1E cells. A, representative confocal images of immunofluorescence staining of WT or ZnT8 KO cells using a proteoliposome- or liposome-immunized serum as indicated. Scale bar, 20 μm. B, histograms of surface immunofluorescence intensities measured in >10,000 WT INS-1E cells that were stained by a proteoliposome- and liposome-immunized serum as indicated. The solid lines are least square fits to a Lorentzian distribution. Arrows indicate serum titrations with increasing concentrations. C, identical experiments in B except that ZnT8 KO INS-1E cells were used. D, saturation of surface immunofluorescence staining with increasing serum concentrations. The concentration-intensity relationships were plotted using flow cytometry data in B and C (mean intensity ± S.E.). The solid lines are hyperbolic fits of concentration-dependent surface staining with a proteoliposome- or liposome-immunized serum as indicated.

    Journal: The Journal of Biological Chemistry

    Article Title: A subclass of serum anti-ZnT8 antibodies directed to the surface of live pancreatic β-cells

    doi: 10.1074/jbc.RA117.000195

    Figure Lengend Snippet: ZnT8-specific surface labeling of live INS-1E cells. A, representative confocal images of immunofluorescence staining of WT or ZnT8 KO cells using a proteoliposome- or liposome-immunized serum as indicated. Scale bar, 20 μm. B, histograms of surface immunofluorescence intensities measured in >10,000 WT INS-1E cells that were stained by a proteoliposome- and liposome-immunized serum as indicated. The solid lines are least square fits to a Lorentzian distribution. Arrows indicate serum titrations with increasing concentrations. C, identical experiments in B except that ZnT8 KO INS-1E cells were used. D, saturation of surface immunofluorescence staining with increasing serum concentrations. The concentration-intensity relationships were plotted using flow cytometry data in B and C (mean intensity ± S.E.). The solid lines are hyperbolic fits of concentration-dependent surface staining with a proteoliposome- or liposome-immunized serum as indicated.

    Article Snippet: We thank Dr. Hao Zhang from the Flow Cytometry and Immunology Core Facility at Johns Hopkins Bloomberg School of Public Health for assistance in flow cytometry data acquisition and analysis.

    Techniques: Labeling, Immunofluorescence, Staining, Concentration Assay, Flow Cytometry