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fcs express flow software cytometry analysis  (Thermo Fisher)


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    Thermo Fisher fcs express flow software cytometry analysis
    Functional analyses of the ancestral and variant genotypes of the CTLA-4 c.-1577G>A. Analysis of CTLA-4 gene expression in peripheral blood of patients with cutaneous melanoma ( A ). Gene expression was higher in patients with AA genotype than in those with GG genotype. Relative luciferase activity in SK-MEL-28 and A-375 melanoma cell lines transfected with the ancestral plasmid (GG genotype) or with the variant plasmid (AA genotype) ( B ). Luciferase activity was higher in cells with AA genotype than in cells with GG genotype. Assessment of the cell cycle in strains modified to present ancestral and variant genotypes ( C ). Cells were identified in the G1, S, and G2 phases using flow <t>cytometry.</t> A higher percentage of SK-MEL-28 cells with the GG genotype was found in the G1 phase compared to those with the AA genotype *, and a higher percentage of SK-MEL-28 cells with the AA genotype was found in S phase compared to those with GG genotype **; a similar percentage of A-375 cells were seen in the G1, S, and G2 phases. Cell proliferation in SK-MEL-28 and A-375 melanoma cell lines ( D ). A higher percentage of SK-MEL-28 and A-375 cells with AA genotype was found in proliferation when compared to those with the GG genotype. Analysis of the assessment of apoptosis and necrosis by flow cytometry with stimulation of the immunotherapy drug ipilimumab ( E ). A higher percentage of SK-MEL-28 cells with GG genotype was found in necrosis compared to those with the AA genotype *; a higher percentage of cells with the AA genotype were alive compared to those with the GG genotype **; the A-375 cells with the GG genotype were in initial apoptosis when compared to cells with the AA genotype.
    Fcs Express Flow Software Cytometry Analysis, supplied by Thermo Fisher, 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/fcs express flow software cytometry analysis/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    fcs express flow software cytometry analysis - by Bioz Stars, 2026-05
    90/100 stars

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    1) Product Images from "Association of Cytotoxic T-Lymphocyte Antigen-4 ( CTLA-4 ) Genetic Variants with Risk and Outcome of Cutaneous Melanoma"

    Article Title: Association of Cytotoxic T-Lymphocyte Antigen-4 ( CTLA-4 ) Genetic Variants with Risk and Outcome of Cutaneous Melanoma

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms252212327

    Functional analyses of the ancestral and variant genotypes of the CTLA-4 c.-1577G>A. Analysis of CTLA-4 gene expression in peripheral blood of patients with cutaneous melanoma ( A ). Gene expression was higher in patients with AA genotype than in those with GG genotype. Relative luciferase activity in SK-MEL-28 and A-375 melanoma cell lines transfected with the ancestral plasmid (GG genotype) or with the variant plasmid (AA genotype) ( B ). Luciferase activity was higher in cells with AA genotype than in cells with GG genotype. Assessment of the cell cycle in strains modified to present ancestral and variant genotypes ( C ). Cells were identified in the G1, S, and G2 phases using flow cytometry. A higher percentage of SK-MEL-28 cells with the GG genotype was found in the G1 phase compared to those with the AA genotype *, and a higher percentage of SK-MEL-28 cells with the AA genotype was found in S phase compared to those with GG genotype **; a similar percentage of A-375 cells were seen in the G1, S, and G2 phases. Cell proliferation in SK-MEL-28 and A-375 melanoma cell lines ( D ). A higher percentage of SK-MEL-28 and A-375 cells with AA genotype was found in proliferation when compared to those with the GG genotype. Analysis of the assessment of apoptosis and necrosis by flow cytometry with stimulation of the immunotherapy drug ipilimumab ( E ). A higher percentage of SK-MEL-28 cells with GG genotype was found in necrosis compared to those with the AA genotype *; a higher percentage of cells with the AA genotype were alive compared to those with the GG genotype **; the A-375 cells with the GG genotype were in initial apoptosis when compared to cells with the AA genotype.
    Figure Legend Snippet: Functional analyses of the ancestral and variant genotypes of the CTLA-4 c.-1577G>A. Analysis of CTLA-4 gene expression in peripheral blood of patients with cutaneous melanoma ( A ). Gene expression was higher in patients with AA genotype than in those with GG genotype. Relative luciferase activity in SK-MEL-28 and A-375 melanoma cell lines transfected with the ancestral plasmid (GG genotype) or with the variant plasmid (AA genotype) ( B ). Luciferase activity was higher in cells with AA genotype than in cells with GG genotype. Assessment of the cell cycle in strains modified to present ancestral and variant genotypes ( C ). Cells were identified in the G1, S, and G2 phases using flow cytometry. A higher percentage of SK-MEL-28 cells with the GG genotype was found in the G1 phase compared to those with the AA genotype *, and a higher percentage of SK-MEL-28 cells with the AA genotype was found in S phase compared to those with GG genotype **; a similar percentage of A-375 cells were seen in the G1, S, and G2 phases. Cell proliferation in SK-MEL-28 and A-375 melanoma cell lines ( D ). A higher percentage of SK-MEL-28 and A-375 cells with AA genotype was found in proliferation when compared to those with the GG genotype. Analysis of the assessment of apoptosis and necrosis by flow cytometry with stimulation of the immunotherapy drug ipilimumab ( E ). A higher percentage of SK-MEL-28 cells with GG genotype was found in necrosis compared to those with the AA genotype *; a higher percentage of cells with the AA genotype were alive compared to those with the GG genotype **; the A-375 cells with the GG genotype were in initial apoptosis when compared to cells with the AA genotype.

    Techniques Used: Functional Assay, Variant Assay, Gene Expression, Luciferase, Activity Assay, Transfection, Plasmid Preparation, Modification, Flow Cytometry



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    Thermo Fisher fcs express flow software cytometry analysis
    Functional analyses of the ancestral and variant genotypes of the CTLA-4 c.-1577G>A. Analysis of CTLA-4 gene expression in peripheral blood of patients with cutaneous melanoma ( A ). Gene expression was higher in patients with AA genotype than in those with GG genotype. Relative luciferase activity in SK-MEL-28 and A-375 melanoma cell lines transfected with the ancestral plasmid (GG genotype) or with the variant plasmid (AA genotype) ( B ). Luciferase activity was higher in cells with AA genotype than in cells with GG genotype. Assessment of the cell cycle in strains modified to present ancestral and variant genotypes ( C ). Cells were identified in the G1, S, and G2 phases using flow <t>cytometry.</t> A higher percentage of SK-MEL-28 cells with the GG genotype was found in the G1 phase compared to those with the AA genotype *, and a higher percentage of SK-MEL-28 cells with the AA genotype was found in S phase compared to those with GG genotype **; a similar percentage of A-375 cells were seen in the G1, S, and G2 phases. Cell proliferation in SK-MEL-28 and A-375 melanoma cell lines ( D ). A higher percentage of SK-MEL-28 and A-375 cells with AA genotype was found in proliferation when compared to those with the GG genotype. Analysis of the assessment of apoptosis and necrosis by flow cytometry with stimulation of the immunotherapy drug ipilimumab ( E ). A higher percentage of SK-MEL-28 cells with GG genotype was found in necrosis compared to those with the AA genotype *; a higher percentage of cells with the AA genotype were alive compared to those with the GG genotype **; the A-375 cells with the GG genotype were in initial apoptosis when compared to cells with the AA genotype.
    Fcs Express Flow Software Cytometry Analysis, supplied by Thermo Fisher, 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/fcs express flow software cytometry analysis/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    fcs express flow software cytometry analysis - by Bioz Stars, 2026-05
    90/100 stars
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    Functional analyses of the ancestral and variant genotypes of the CTLA-4 c.-1577G>A. Analysis of CTLA-4 gene expression in peripheral blood of patients with cutaneous melanoma ( A ). Gene expression was higher in patients with AA genotype than in those with GG genotype. Relative luciferase activity in SK-MEL-28 and A-375 melanoma cell lines transfected with the ancestral plasmid (GG genotype) or with the variant plasmid (AA genotype) ( B ). Luciferase activity was higher in cells with AA genotype than in cells with GG genotype. Assessment of the cell cycle in strains modified to present ancestral and variant genotypes ( C ). Cells were identified in the G1, S, and G2 phases using flow cytometry. A higher percentage of SK-MEL-28 cells with the GG genotype was found in the G1 phase compared to those with the AA genotype *, and a higher percentage of SK-MEL-28 cells with the AA genotype was found in S phase compared to those with GG genotype **; a similar percentage of A-375 cells were seen in the G1, S, and G2 phases. Cell proliferation in SK-MEL-28 and A-375 melanoma cell lines ( D ). A higher percentage of SK-MEL-28 and A-375 cells with AA genotype was found in proliferation when compared to those with the GG genotype. Analysis of the assessment of apoptosis and necrosis by flow cytometry with stimulation of the immunotherapy drug ipilimumab ( E ). A higher percentage of SK-MEL-28 cells with GG genotype was found in necrosis compared to those with the AA genotype *; a higher percentage of cells with the AA genotype were alive compared to those with the GG genotype **; the A-375 cells with the GG genotype were in initial apoptosis when compared to cells with the AA genotype.

    Journal: International Journal of Molecular Sciences

    Article Title: Association of Cytotoxic T-Lymphocyte Antigen-4 ( CTLA-4 ) Genetic Variants with Risk and Outcome of Cutaneous Melanoma

    doi: 10.3390/ijms252212327

    Figure Lengend Snippet: Functional analyses of the ancestral and variant genotypes of the CTLA-4 c.-1577G>A. Analysis of CTLA-4 gene expression in peripheral blood of patients with cutaneous melanoma ( A ). Gene expression was higher in patients with AA genotype than in those with GG genotype. Relative luciferase activity in SK-MEL-28 and A-375 melanoma cell lines transfected with the ancestral plasmid (GG genotype) or with the variant plasmid (AA genotype) ( B ). Luciferase activity was higher in cells with AA genotype than in cells with GG genotype. Assessment of the cell cycle in strains modified to present ancestral and variant genotypes ( C ). Cells were identified in the G1, S, and G2 phases using flow cytometry. A higher percentage of SK-MEL-28 cells with the GG genotype was found in the G1 phase compared to those with the AA genotype *, and a higher percentage of SK-MEL-28 cells with the AA genotype was found in S phase compared to those with GG genotype **; a similar percentage of A-375 cells were seen in the G1, S, and G2 phases. Cell proliferation in SK-MEL-28 and A-375 melanoma cell lines ( D ). A higher percentage of SK-MEL-28 and A-375 cells with AA genotype was found in proliferation when compared to those with the GG genotype. Analysis of the assessment of apoptosis and necrosis by flow cytometry with stimulation of the immunotherapy drug ipilimumab ( E ). A higher percentage of SK-MEL-28 cells with GG genotype was found in necrosis compared to those with the AA genotype *; a higher percentage of cells with the AA genotype were alive compared to those with the GG genotype **; the A-375 cells with the GG genotype were in initial apoptosis when compared to cells with the AA genotype.

    Article Snippet: The intensity of 7-AAD labeling and separation of cell cycle phases G1, S, and G2 were analyzed by the FCS Express Flow software Cytometry Analysis ( https://denovosoftware.com/ ) (Thermo Fisher Scientific, Waltham, MA, USA).

    Techniques: Functional Assay, Variant Assay, Gene Expression, Luciferase, Activity Assay, Transfection, Plasmid Preparation, Modification, Flow Cytometry