Review




Structured Review

Becton Dickinson software v10.6.2
Software V10.6.2, supplied by Becton Dickinson, 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/product/flow+data+analyses/v10+software/pmc10036595-84-9-10
Average 90 stars, based on 1 article reviews
software v10.6.2 - by Bioz Stars, 2026-11
90/100 stars

Images

Related Articles

Flow Cytometry:

Article Title: HPN328, a Trispecific T Cell–Activating Protein Construct Targeting DLL3-Expressing Solid Tumors
Article Snippet: The samples were analyzed on FACSCelesta (BD Biosciences). .. Flow cytometry data were processed using FlowJo v10 software (FlowJo, LLC). ..

Article Title: The Wdr5-H3K4me3 Epigenetic Axis Regulates Pancreatic Tumor Immunogenicity and Immune Suppression.
Article Snippet: Stained cells were analyzed by flow cytometry (BD FACS Verse). .. All flow cytometry data were analyzed using FlowJo v10 software (BD Biosciences, San Diego, CA, USA). ..

Cytometry:

Article Title: HPN328, a Trispecific T Cell–Activating Protein Construct Targeting DLL3-Expressing Solid Tumors
Article Snippet: The samples were analyzed on FACSCelesta (BD Biosciences). .. Flow cytometry data were processed using FlowJo v10 software (FlowJo, LLC). ..

Software:

Article Title: HPN328, a Trispecific T Cell–Activating Protein Construct Targeting DLL3-Expressing Solid Tumors
Article Snippet: The samples were analyzed on FACSCelesta (BD Biosciences). .. Flow cytometry data were processed using FlowJo v10 software (FlowJo, LLC). ..

Article Title: Enhancing HLA-DR in Cytotoxic T Lymphocytes is crucial for the development of efficient adoptive T cell Therapies for Breast Cancer
Article Snippet: Cell viability was determined with BD Horizon TM Fixable Viability Stain 450 (BD Biosciences) incubated with the cell suspension for 20 minutes in the dark at 4°C. .. Data acquisition was conducted using the BD Fluorescence Activated Cell Sorting (FACS) Canto II with FACSDiva Software v8 (BD Biosciences), and the results were analyzed using FlowJo software v10. ..

Article Title: Defining cell type-specific immune responses in a mouse model of allergic contact dermatitis by single-cell transcriptomics
Article Snippet: To stain intracellular proteins in immune cells, stained cells were then fixed and permeabilized using the intracellular fixation and permeabilization buffer set (eBioscience, #00-8333-56) and stained by FITC-IL4 (BioLegend, #504109), FITC-IL13 (eBioscience, #53-7133-82), AF700-IFNG (BioLegend, #505824), PE-IL17A (eBioscience, #12-7177-81). .. FACS analysis for protein expression of each cell marker was performed by the Thermo Attune NxT machine and analyzed by FlowJo V10 software. ..

Article Title: The Wdr5-H3K4me3 Epigenetic Axis Regulates Pancreatic Tumor Immunogenicity and Immune Suppression.
Article Snippet: Stained cells were analyzed by flow cytometry (BD FACS Verse). .. All flow cytometry data were analyzed using FlowJo v10 software (BD Biosciences, San Diego, CA, USA). ..

other:

Article Title: Procaine induces cell cycle arrest, apoptosis and autophagy through the inhibition of the PI3K/AKT and ERK pathways in human tongue squamous cell carcinoma
Article Snippet: The results of cell cycle analysis were statistically analyzed to obtain peak plots using FlowJo software v10.6.2 (BD Biosciences).

Article Title: Dynamic changes in immune cells in humanized liver metastasis and subcutaneous xenograft mouse models
Article Snippet: The data were analyzed using FlowJo v10.6.2. software (BD Biosciences).

Article Title: Procaine induces cell cycle arrest, apoptosis and autophagy through the inhibition of the PI3K/AKT and ERK pathways in human tongue squamous cell carcinoma
Article Snippet: The results of cell flow analysis were statistically analyzed to obtain peak plots using FlowJo software v10.6.2 (BD Biosciences).

Article Title: Procaine induces cell cycle arrest, apoptosis and autophagy through the inhibition of the PI3K/AKT and ERK pathways in human tongue squamous cell carcinoma
Article Snippet: The results of apoptosis analysis were statistically analyzed by using FlowJo software v10.6.2 (BD Biosciences).

Fluorescence:

Article Title: Enhancing HLA-DR in Cytotoxic T Lymphocytes is crucial for the development of efficient adoptive T cell Therapies for Breast Cancer
Article Snippet: Cell viability was determined with BD Horizon TM Fixable Viability Stain 450 (BD Biosciences) incubated with the cell suspension for 20 minutes in the dark at 4°C. .. Data acquisition was conducted using the BD Fluorescence Activated Cell Sorting (FACS) Canto II with FACSDiva Software v8 (BD Biosciences), and the results were analyzed using FlowJo software v10. ..

FACS:

Article Title: Enhancing HLA-DR in Cytotoxic T Lymphocytes is crucial for the development of efficient adoptive T cell Therapies for Breast Cancer
Article Snippet: Cell viability was determined with BD Horizon TM Fixable Viability Stain 450 (BD Biosciences) incubated with the cell suspension for 20 minutes in the dark at 4°C. .. Data acquisition was conducted using the BD Fluorescence Activated Cell Sorting (FACS) Canto II with FACSDiva Software v8 (BD Biosciences), and the results were analyzed using FlowJo software v10. ..

Article Title: Defining cell type-specific immune responses in a mouse model of allergic contact dermatitis by single-cell transcriptomics
Article Snippet: To stain intracellular proteins in immune cells, stained cells were then fixed and permeabilized using the intracellular fixation and permeabilization buffer set (eBioscience, #00-8333-56) and stained by FITC-IL4 (BioLegend, #504109), FITC-IL13 (eBioscience, #53-7133-82), AF700-IFNG (BioLegend, #505824), PE-IL17A (eBioscience, #12-7177-81). .. FACS analysis for protein expression of each cell marker was performed by the Thermo Attune NxT machine and analyzed by FlowJo V10 software. ..

Expressing:

Article Title: Defining cell type-specific immune responses in a mouse model of allergic contact dermatitis by single-cell transcriptomics
Article Snippet: To stain intracellular proteins in immune cells, stained cells were then fixed and permeabilized using the intracellular fixation and permeabilization buffer set (eBioscience, #00-8333-56) and stained by FITC-IL4 (BioLegend, #504109), FITC-IL13 (eBioscience, #53-7133-82), AF700-IFNG (BioLegend, #505824), PE-IL17A (eBioscience, #12-7177-81). .. FACS analysis for protein expression of each cell marker was performed by the Thermo Attune NxT machine and analyzed by FlowJo V10 software. ..

Marker:

Article Title: Defining cell type-specific immune responses in a mouse model of allergic contact dermatitis by single-cell transcriptomics
Article Snippet: To stain intracellular proteins in immune cells, stained cells were then fixed and permeabilized using the intracellular fixation and permeabilization buffer set (eBioscience, #00-8333-56) and stained by FITC-IL4 (BioLegend, #504109), FITC-IL13 (eBioscience, #53-7133-82), AF700-IFNG (BioLegend, #505824), PE-IL17A (eBioscience, #12-7177-81). .. FACS analysis for protein expression of each cell marker was performed by the Thermo Attune NxT machine and analyzed by FlowJo V10 software. ..



Similar Products

90
GraphPad Software Inc flow cytometry data analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Cytometry Data Analyses, supplied by GraphPad Software Inc, 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/product/flow+data+analyses/flow+cytometry/bio_rxiv__2025__07__17__664572-53-4-10
Average 90 stars, based on 1 article reviews
flow cytometry data analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

90
Tree Star Inc flow data analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Data Analyses, supplied by Tree Star Inc, 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/product/flow+data+analyses/flow+data+analyses/pmc10173990__jitc___2023___006930supp001-25-12-19
Average 90 stars, based on 1 article reviews
flow data analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

90
GraphPad Software Inc flow cytometry data statistical analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Cytometry Data Statistical Analyses, supplied by GraphPad Software Inc, 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/product/flow+data+analyses/flow+cytometry/pm32620016-78-1-9
Average 90 stars, based on 1 article reviews
flow cytometry data statistical analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

90
GraphPad Software Inc flow cytometric and clinical data analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Cytometric And Clinical Data Analyses, supplied by GraphPad Software Inc, 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/product/flow+data+analyses/flow+cytometry+data+analysis+software/10__1080_slash_2162402x__2019__1665460-64-12-20
Average 90 stars, based on 1 article reviews
flow cytometric and clinical data analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

90
Danaher Inc flow data analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Data Analyses, supplied by Danaher Inc, 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/product/flow+data+analyses/flow+data+analyses/10__1097_slash_cji__0000000000000216-62-1-15
Average 90 stars, based on 1 article reviews
flow data analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

90
Tree Star Inc flow cytometer data analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Cytometer Data Analyses, supplied by Tree Star Inc, 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/product/flow+data+analyses/flow+cytometer/pmc04965085-90-1-13
Average 90 stars, based on 1 article reviews
flow cytometer data analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

90
Glaxo Smith flow cytometry data analyses
Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing <t>flow-cytometry</t> data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.
Flow Cytometry Data Analyses, supplied by Glaxo Smith, 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/product/flow+data+analyses/flow+cytometry/pm23419064-39-8-20
Average 90 stars, based on 1 article reviews
flow cytometry data analyses - by Bioz Stars, 2026-11
90/100 stars
  Buy from Supplier

Image Search Results


Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing flow-cytometry data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.

Journal: bioRxiv

Article Title: A 3-genes interferon signature predicts sustained complete remission in pediatric AML patients

doi: 10.1101/2025.07.17.664572

Figure Lengend Snippet: Lymphocyte profiling of the L-TME in pediatric AML patients. (a) Logical gating strategy showing the T cell composition of L-TME in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. The data are displayed cumulatively in the dot plots and individually in the graphs (c and e). The same cumulative and individual representation is depicted in all figures showing flow-cytometry data. (b) I) Cumulative plots displaying CD45 + /CD34 − /CD19 − and CD3 − myeloid cells in AML patients with (top row, n=4 ) and without (bottom row, n=5 ) sustained-CR. II-III) Individual values of samples in (a) and (b) are displayed in a graph; Q value is the result of FDR-corrected multiple t-tests between sustained (red) and non-sustained (black) patients’ samples. Only significant differences are shown. IV) The % of blasts scored in the patients’ diagnosis for all the cohort is displayed in the graph for patients with and without sustained-CR. The blast score was calculated by a combination of microscope and clinical flow-cytometry analyses and provided as clinical report for patients in the Pathology Laboratory of Sidra. (c) I) Phenotype of the CD4 dim cell population: the majority of the cells are IFNγ + (shown in the colored Z-axis) CD4 + and CD8 + doublets, engaging in close networking interactions. A full panel of expression markers for this population is shown in Supplementary Figure 1b. II) Individual values of samples in (b) show a trend of enrichment in CD4 dim doublets (considering lower singlets) in patients without long-term remission.

Article Snippet: Statistical analyses of the flow cytometry data were performed using GraphPad Prism (v. 10.3.1).

Techniques: Flow Cytometry, Biomarker Discovery, Microscopy, Expressing