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raw cytof fcs files  (Mendeley Ltd)

 
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    Mendeley Ltd raw cytof fcs files
    Raw Cytof Fcs Files, supplied by Mendeley Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytof+fcs+files/files+files+fsa+fsa+raw/pm41520339-292-0-16
    Average 86 stars, based on 1 article reviews
    raw cytof fcs files - by Bioz Stars, 2026-09
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    other:

    Article Title: High-grade serous ovarian tumor cells modulate NK cell function to create an immune-tolerant microenvironment.
    Article Snippet: d Two datasets; 17 CyTOF FCS files for NK/T cell tumor infiltrates and 12 CyTOF FCS files for tumor cells have been deposited at Mendeley Data andwill bemade publicly available as of the date of publication.

    Software:

    Article Title: Fibrinogen-like protein 1 is a major immune inhibitory ligand of LAG3
    Article Snippet: .. DATA AND SOFTWARE AVAILABILITY The CyTOF FCS files associated with the datasets in this paper have been uploaded in Mendeley database with the following preview link: https://data.mendeley.com/datasets/8gvfpy83jn/draft?a=e1bb6f8d-a1f8-481f-a465-142dabd0f24b Supplemental Excel Table: Supplemental Table S1 . ..



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    cytof fcs files  (Johns Hopkins HealthCare)
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    A, Volcano plot depicting differentially secreted proteins in Cx3cr1 -PAC −/− (left) or LysM -PAC −/− (right) peritoneal fluids after 4 hours of peritoneal infection. Highlighted proteins represent top differentially secreted proteins with p < 0.05 and average log-transformed fold-change > 0.25. B , Quantification of highlighted proteins in ( A ), excluding proteins with absolute concentration below 100 pg/mL. Each genotype has n = 6 mice in independent experiments. C , UMAP color-coded for immune cell types based on the expression of cell-type enriched surface markers before and after infection. NK, natural killer cells. DCs, dendritic cells. D , FlowSOM analyzed colored tree for immune cell types based on the expression of cell-type enriched surface markers post-infection in control (left) or LysM -PAC −/− (right) peritoneal fluids. E , Donut plots depicting composition of peritoneal immune cell types with respect to genotypes and treatments quantified with manual gating. F , Manual gating strategy of indicated immune cell types in <t>cyTOF</t> dataset. DN, double negative. G , Quantification of neutrophil and Ly6C high monocyte populations through manual gating strategy. Each condition and genotype have at least n > 3 mice in independent experiments. All control groups represent Pacc1 F/F genotype. Data are reported as mean ± SEM. Unpaired t-test for B . Two-way ANOVA with Sidak’s test for G . *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    A, Volcano plot depicting differentially secreted proteins in Cx3cr1 -PAC −/− (left) or LysM -PAC −/− (right) peritoneal fluids after 4 hours of peritoneal infection. Highlighted proteins represent top differentially secreted proteins with p < 0.05 and average log-transformed fold-change > 0.25. B , Quantification of highlighted proteins in ( A ), excluding proteins with absolute concentration below 100 pg/mL. Each genotype has n = 6 mice in independent experiments. C , UMAP color-coded for immune cell types based on the expression of cell-type enriched surface markers before and after infection. NK, natural killer cells. DCs, dendritic cells. D , FlowSOM analyzed colored tree for immune cell types based on the expression of cell-type enriched surface markers post-infection in control (left) or LysM -PAC −/− (right) peritoneal fluids. E , Donut plots depicting composition of peritoneal immune cell types with respect to genotypes and treatments quantified with manual gating. F , Manual gating strategy of indicated immune cell types in <t>cyTOF</t> dataset. DN, double negative. G , Quantification of neutrophil and Ly6C high monocyte populations through manual gating strategy. Each condition and genotype have at least n > 3 mice in independent experiments. All control groups represent Pacc1 F/F genotype. Data are reported as mean ± SEM. Unpaired t-test for B . Two-way ANOVA with Sidak’s test for G . *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    A, Volcano plot depicting differentially secreted proteins in Cx3cr1 -PAC −/− (left) or LysM -PAC −/− (right) peritoneal fluids after 4 hours of peritoneal infection. Highlighted proteins represent top differentially secreted proteins with p < 0.05 and average log-transformed fold-change > 0.25. B , Quantification of highlighted proteins in ( A ), excluding proteins with absolute concentration below 100 pg/mL. Each genotype has n = 6 mice in independent experiments. C , UMAP color-coded for immune cell types based on the expression of cell-type enriched surface markers before and after infection. NK, natural killer cells. DCs, dendritic cells. D , FlowSOM analyzed colored tree for immune cell types based on the expression of cell-type enriched surface markers post-infection in control (left) or LysM -PAC −/− (right) peritoneal fluids. E , Donut plots depicting composition of peritoneal immune cell types with respect to genotypes and treatments quantified with manual gating. F , Manual gating strategy of indicated immune cell types in <t>cyTOF</t> dataset. DN, double negative. G , Quantification of neutrophil and Ly6C high monocyte populations through manual gating strategy. Each condition and genotype have at least n > 3 mice in independent experiments. All control groups represent Pacc1 F/F genotype. Data are reported as mean ± SEM. Unpaired t-test for B . Two-way ANOVA with Sidak’s test for G . *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    cytof fcs files  (Mendeley Ltd)
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    A, Volcano plot depicting differentially secreted proteins in Cx3cr1 -PAC −/− (left) or LysM -PAC −/− (right) peritoneal fluids after 4 hours of peritoneal infection. Highlighted proteins represent top differentially secreted proteins with p < 0.05 and average log-transformed fold-change > 0.25. B , Quantification of highlighted proteins in ( A ), excluding proteins with absolute concentration below 100 pg/mL. Each genotype has n = 6 mice in independent experiments. C , UMAP color-coded for immune cell types based on the expression of cell-type enriched surface markers before and after infection. NK, natural killer cells. DCs, dendritic cells. D , FlowSOM analyzed colored tree for immune cell types based on the expression of cell-type enriched surface markers post-infection in control (left) or LysM -PAC −/− (right) peritoneal fluids. E , Donut plots depicting composition of peritoneal immune cell types with respect to genotypes and treatments quantified with manual gating. F , Manual gating strategy of indicated immune cell types in <t>cyTOF</t> dataset. DN, double negative. G , Quantification of neutrophil and Ly6C high monocyte populations through manual gating strategy. Each condition and genotype have at least n > 3 mice in independent experiments. All control groups represent Pacc1 F/F genotype. Data are reported as mean ± SEM. Unpaired t-test for B . Two-way ANOVA with Sidak’s test for G . *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.
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    A, Volcano plot depicting differentially secreted proteins in Cx3cr1 -PAC −/− (left) or LysM -PAC −/− (right) peritoneal fluids after 4 hours of peritoneal infection. Highlighted proteins represent top differentially secreted proteins with p < 0.05 and average log-transformed fold-change > 0.25. B , Quantification of highlighted proteins in ( A ), excluding proteins with absolute concentration below 100 pg/mL. Each genotype has n = 6 mice in independent experiments. C , UMAP color-coded for immune cell types based on the expression of cell-type enriched surface markers before and after infection. NK, natural killer cells. DCs, dendritic cells. D , FlowSOM analyzed colored tree for immune cell types based on the expression of cell-type enriched surface markers post-infection in control (left) or LysM -PAC −/− (right) peritoneal fluids. E , Donut plots depicting composition of peritoneal immune cell types with respect to genotypes and treatments quantified with manual gating. F , Manual gating strategy of indicated immune cell types in cyTOF dataset. DN, double negative. G , Quantification of neutrophil and Ly6C high monocyte populations through manual gating strategy. Each condition and genotype have at least n > 3 mice in independent experiments. All control groups represent Pacc1 F/F genotype. Data are reported as mean ± SEM. Unpaired t-test for B . Two-way ANOVA with Sidak’s test for G . *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

    Journal: bioRxiv

    Article Title: The phagosome-mediated anti-bacterial immunity is governed by the proton-activated chloride channel in peritoneal macrophages

    doi: 10.1101/2025.02.27.640612

    Figure Lengend Snippet: A, Volcano plot depicting differentially secreted proteins in Cx3cr1 -PAC −/− (left) or LysM -PAC −/− (right) peritoneal fluids after 4 hours of peritoneal infection. Highlighted proteins represent top differentially secreted proteins with p < 0.05 and average log-transformed fold-change > 0.25. B , Quantification of highlighted proteins in ( A ), excluding proteins with absolute concentration below 100 pg/mL. Each genotype has n = 6 mice in independent experiments. C , UMAP color-coded for immune cell types based on the expression of cell-type enriched surface markers before and after infection. NK, natural killer cells. DCs, dendritic cells. D , FlowSOM analyzed colored tree for immune cell types based on the expression of cell-type enriched surface markers post-infection in control (left) or LysM -PAC −/− (right) peritoneal fluids. E , Donut plots depicting composition of peritoneal immune cell types with respect to genotypes and treatments quantified with manual gating. F , Manual gating strategy of indicated immune cell types in cyTOF dataset. DN, double negative. G , Quantification of neutrophil and Ly6C high monocyte populations through manual gating strategy. Each condition and genotype have at least n > 3 mice in independent experiments. All control groups represent Pacc1 F/F genotype. Data are reported as mean ± SEM. Unpaired t-test for B . Two-way ANOVA with Sidak’s test for G . *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001.

    Article Snippet: cyTOF FCS files acquired and exported from the Johns Hopkins SKCCC Flow/Mass Cytometry Core were uploaded to OMIQ.

    Techniques: Infection, Transformation Assay, Concentration Assay, Expressing, Control