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flow cytometric data analysis software  (GraphPad Software Inc)


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    Structured Review

    GraphPad Software Inc flow cytometric data analysis software
    Flow <t>cytometric</t> data comparing patients with CTLA4h with active neuroinflammatory lesions on MRI (black), a prior history of neuroinflammatory lesions (green), and no history of inflammatory lesions (orange) on MRI with a cohort of healthy controls (NDs, white circles). All graphs depict values from blood (left half of each panel) and CSF (right half). (A) Total frequency of CD4+ and CD8+ T cells within total lymphocyte counts and the ratio of CD4+ to CD8+ T cells. (B) Percentage of memory T cell subtypes (CD45RA–CD27+) in CD4+ T cells and CD8+ T cells, and memory Tfh cells (CD45RA–CXCR5+) in CD4+ T cells (right). (C) Frequency of total B cells and memory B cell subtypes, including unswitched memory (IgD+CD27+) and switched memory (IgD–CD27+) B cells. For all flow cytometric data, the Mann-Whitney U test was performed for comparisons between ND and CTLA4 cohorts, within each compartment (i.e., peripheral blood and CSF). Significance was set at P < 0.05. Each flow cytometric experiment for lymphocyte subsets from peripheral blood that was paired with a CSF sample obtained at the same time represents a single experiment, given the nature of the specimen (CSF obtained by LP) and the limited amount of specimen that could be obtained, as well as the sensitivity for the timing of the procedure according to the clinical status and the treatment course of the patient.
    Flow Cytometric Data Analysis Software, 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/result/flow cytometric data analysis software/product/GraphPad Software Inc
    Average 90 stars, based on 1 article reviews
    flow cytometric data analysis software - by Bioz Stars, 2026-06
    90/100 stars

    Images

    1) Product Images from "Haploinsufficiency of immune checkpoint receptor CTLA4 induces a distinct neuroinflammatory disorder"

    Article Title: Haploinsufficiency of immune checkpoint receptor CTLA4 induces a distinct neuroinflammatory disorder

    Journal: The Journal of Clinical Investigation

    doi: 10.1172/JCI135947

    Flow cytometric data comparing patients with CTLA4h with active neuroinflammatory lesions on MRI (black), a prior history of neuroinflammatory lesions (green), and no history of inflammatory lesions (orange) on MRI with a cohort of healthy controls (NDs, white circles). All graphs depict values from blood (left half of each panel) and CSF (right half). (A) Total frequency of CD4+ and CD8+ T cells within total lymphocyte counts and the ratio of CD4+ to CD8+ T cells. (B) Percentage of memory T cell subtypes (CD45RA–CD27+) in CD4+ T cells and CD8+ T cells, and memory Tfh cells (CD45RA–CXCR5+) in CD4+ T cells (right). (C) Frequency of total B cells and memory B cell subtypes, including unswitched memory (IgD+CD27+) and switched memory (IgD–CD27+) B cells. For all flow cytometric data, the Mann-Whitney U test was performed for comparisons between ND and CTLA4 cohorts, within each compartment (i.e., peripheral blood and CSF). Significance was set at P < 0.05. Each flow cytometric experiment for lymphocyte subsets from peripheral blood that was paired with a CSF sample obtained at the same time represents a single experiment, given the nature of the specimen (CSF obtained by LP) and the limited amount of specimen that could be obtained, as well as the sensitivity for the timing of the procedure according to the clinical status and the treatment course of the patient.
    Figure Legend Snippet: Flow cytometric data comparing patients with CTLA4h with active neuroinflammatory lesions on MRI (black), a prior history of neuroinflammatory lesions (green), and no history of inflammatory lesions (orange) on MRI with a cohort of healthy controls (NDs, white circles). All graphs depict values from blood (left half of each panel) and CSF (right half). (A) Total frequency of CD4+ and CD8+ T cells within total lymphocyte counts and the ratio of CD4+ to CD8+ T cells. (B) Percentage of memory T cell subtypes (CD45RA–CD27+) in CD4+ T cells and CD8+ T cells, and memory Tfh cells (CD45RA–CXCR5+) in CD4+ T cells (right). (C) Frequency of total B cells and memory B cell subtypes, including unswitched memory (IgD+CD27+) and switched memory (IgD–CD27+) B cells. For all flow cytometric data, the Mann-Whitney U test was performed for comparisons between ND and CTLA4 cohorts, within each compartment (i.e., peripheral blood and CSF). Significance was set at P < 0.05. Each flow cytometric experiment for lymphocyte subsets from peripheral blood that was paired with a CSF sample obtained at the same time represents a single experiment, given the nature of the specimen (CSF obtained by LP) and the limited amount of specimen that could be obtained, as well as the sensitivity for the timing of the procedure according to the clinical status and the treatment course of the patient.

    Techniques Used: MANN-WHITNEY



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    GraphPad Software Inc flow cytometric data analysis software
    Flow <t>cytometric</t> data comparing patients with CTLA4h with active neuroinflammatory lesions on MRI (black), a prior history of neuroinflammatory lesions (green), and no history of inflammatory lesions (orange) on MRI with a cohort of healthy controls (NDs, white circles). All graphs depict values from blood (left half of each panel) and CSF (right half). (A) Total frequency of CD4+ and CD8+ T cells within total lymphocyte counts and the ratio of CD4+ to CD8+ T cells. (B) Percentage of memory T cell subtypes (CD45RA–CD27+) in CD4+ T cells and CD8+ T cells, and memory Tfh cells (CD45RA–CXCR5+) in CD4+ T cells (right). (C) Frequency of total B cells and memory B cell subtypes, including unswitched memory (IgD+CD27+) and switched memory (IgD–CD27+) B cells. For all flow cytometric data, the Mann-Whitney U test was performed for comparisons between ND and CTLA4 cohorts, within each compartment (i.e., peripheral blood and CSF). Significance was set at P < 0.05. Each flow cytometric experiment for lymphocyte subsets from peripheral blood that was paired with a CSF sample obtained at the same time represents a single experiment, given the nature of the specimen (CSF obtained by LP) and the limited amount of specimen that could be obtained, as well as the sensitivity for the timing of the procedure according to the clinical status and the treatment course of the patient.
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    Image Search Results


    Flow cytometric data comparing patients with CTLA4h with active neuroinflammatory lesions on MRI (black), a prior history of neuroinflammatory lesions (green), and no history of inflammatory lesions (orange) on MRI with a cohort of healthy controls (NDs, white circles). All graphs depict values from blood (left half of each panel) and CSF (right half). (A) Total frequency of CD4+ and CD8+ T cells within total lymphocyte counts and the ratio of CD4+ to CD8+ T cells. (B) Percentage of memory T cell subtypes (CD45RA–CD27+) in CD4+ T cells and CD8+ T cells, and memory Tfh cells (CD45RA–CXCR5+) in CD4+ T cells (right). (C) Frequency of total B cells and memory B cell subtypes, including unswitched memory (IgD+CD27+) and switched memory (IgD–CD27+) B cells. For all flow cytometric data, the Mann-Whitney U test was performed for comparisons between ND and CTLA4 cohorts, within each compartment (i.e., peripheral blood and CSF). Significance was set at P < 0.05. Each flow cytometric experiment for lymphocyte subsets from peripheral blood that was paired with a CSF sample obtained at the same time represents a single experiment, given the nature of the specimen (CSF obtained by LP) and the limited amount of specimen that could be obtained, as well as the sensitivity for the timing of the procedure according to the clinical status and the treatment course of the patient.

    Journal: The Journal of Clinical Investigation

    Article Title: Haploinsufficiency of immune checkpoint receptor CTLA4 induces a distinct neuroinflammatory disorder

    doi: 10.1172/JCI135947

    Figure Lengend Snippet: Flow cytometric data comparing patients with CTLA4h with active neuroinflammatory lesions on MRI (black), a prior history of neuroinflammatory lesions (green), and no history of inflammatory lesions (orange) on MRI with a cohort of healthy controls (NDs, white circles). All graphs depict values from blood (left half of each panel) and CSF (right half). (A) Total frequency of CD4+ and CD8+ T cells within total lymphocyte counts and the ratio of CD4+ to CD8+ T cells. (B) Percentage of memory T cell subtypes (CD45RA–CD27+) in CD4+ T cells and CD8+ T cells, and memory Tfh cells (CD45RA–CXCR5+) in CD4+ T cells (right). (C) Frequency of total B cells and memory B cell subtypes, including unswitched memory (IgD+CD27+) and switched memory (IgD–CD27+) B cells. For all flow cytometric data, the Mann-Whitney U test was performed for comparisons between ND and CTLA4 cohorts, within each compartment (i.e., peripheral blood and CSF). Significance was set at P < 0.05. Each flow cytometric experiment for lymphocyte subsets from peripheral blood that was paired with a CSF sample obtained at the same time represents a single experiment, given the nature of the specimen (CSF obtained by LP) and the limited amount of specimen that could be obtained, as well as the sensitivity for the timing of the procedure according to the clinical status and the treatment course of the patient.

    Article Snippet: Statistical analysis of flow cytometric data was performed using GraphPad Prism (GraphPad Software).

    Techniques: MANN-WHITNEY