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human tumor cell lines jurkat  (ATCC)


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    ATCC human tumor cell lines jurkat
    Human Tumor Cell Lines Jurkat, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 4501 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/jurkat+cell+line/Jurkat%2C+Clone+E6-1/us12655213-676-0-20
    Average 99 stars, based on 4501 article reviews
    human tumor cell lines jurkat - by Bioz Stars, 2026-10
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    Cell Culture:

    Article Title: Dean migration mechanisms: facilitating the control of microbial contaminants in cell therapy product manufacturing.
    Article Snippet: .. The Jurkat cell line (human T-lymphocytes, ATCC TIB152) was maintained in RPMI 1640 medium (GIBCO, USA) supplemented with 10% fetal bovine serum (Gibco, USA) and 1% penicillin-streptomycin solution (Gibco, USA), cultured at 37 °C under 5% CO2 in a humidified incubator (Thermo Heracell 150i, USA). ..

    Article Title: Development of a Novel Immunoprotective Culture System for Parathyroid Allografts: Utilizing Static Magnetic Fields to Modulate Lymphocyte Migration
    Article Snippet: Cells were harvested using 0.25% trypsin-EDTA (1X, Gibco, Waltham, MA, USA) prior to the encapsulation process. .. The Jurkat cell line (ATCC, #TIB-152TM) served as the lymphocyte model. Jurkat cells were cultured in complete RPMI-1640 (1X, Gibco, Waltham, MA, USA) medium supplemented with 10% (v/v) FBS and 1% (v/v) P/S. ..

    Article Title: Development of a Novel Immunoprotective Culture System for Parathyroid Allografts: Utilizing Static Magnetic Fields to Modulate Lymphocyte Migration
    Article Snippet: Cells were harvested using 0.25% trypsin-EDTA (1X, Gibco, Waltham, MA, USA) prior to the encapsulation process. .. The Jurkat cell line (ATCC, #TIB-152TM) served as the lymphocyte model. Jurkat cells were cultured in complete RPMI-1640 (1X, Gibco, Waltham, MA, USA) medium supplemented with 10% ( v / v ) FBS and 1% ( v / v ) P/S. ..

    Article Title: T Cell Receptor Co-Stimulation Through Magnetogenetic Tools: A Platform for Wireless Rewiring of Cellular Signaling
    Article Snippet: Normal HEK293T (Hek) cells, obtained from the American Type Culture Collection (ATCC), were cultured at 37 °C with 5% CO2 in DMEM supplemented with 10% fetal bovine serum (FBS) and 1% PenStrep (100 U/mL penicillin and 100 μg/mL streptomycin). .. The Jurkat cell line, obtained from ATCC (Clone E6-1), was cultured under the same conditions but in RPMI medium. ..

    Article Title: Dean migration mechanisms: facilitating the control of microbial contaminants in cell therapy product manufacturing
    Article Snippet: .. The Jurkat cell line (human T-lymphocytes, ATCC TIB-152) was maintained in RPMI 1640 medium (GIBCO, USA) supplemented with 10% fetal bovine serum (Gibco, USA) and 1% penicillin-streptomycin solution (Gibco, USA), cultured at 37 °C under 5% CO 2 in a humidified incubator (Thermo Heracell 150i, USA). ..



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    Image Search Results


    Selective activation of SBT777101 Jurkat reporter cells by citrullinated proteins. Representative dose–response curves showing fold-increase in luminescence ( y -axis) relative to baseline following incubation with increasing concentrations (log scale, x -axis) of citrullinated (red) or noncitrullinated (black) protein targets. Data points represent the mean ± SD of 3 replicates.

    Journal: Toxicological Sciences

    Article Title: Nonclinical safety assessment of SBT777101, a CAR-engineered regulatory T cell therapy for autoimmune diseases

    doi: 10.1093/toxsci/kfag125

    Figure Lengend Snippet: Selective activation of SBT777101 Jurkat reporter cells by citrullinated proteins. Representative dose–response curves showing fold-increase in luminescence ( y -axis) relative to baseline following incubation with increasing concentrations (log scale, x -axis) of citrullinated (red) or noncitrullinated (black) protein targets. Data points represent the mean ± SD of 3 replicates.

    Article Snippet: NFAT-luciferase reporter Jurkat cells (BPS Bioscience) were stably transduced with the SBT777101 CAR.

    Techniques: Activation Assay, Incubation

    Cytotoxicity of BEA, ENN B and MON in cultured human Jurkat T cells (1 × 10 4 cells/well), based on IC 50 value, determined using MTT assay. Cells were treated for 24 h with tested mycotoxins at variable concentrations.

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Cytotoxicity of BEA, ENN B and MON in cultured human Jurkat T cells (1 × 10 4 cells/well), based on IC 50 value, determined using MTT assay. Cells were treated for 24 h with tested mycotoxins at variable concentrations.

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: Cell Culture, MTT Assay

    Effects of beauvericin (BEA), enniatin B (ENN B), and moniliformin (MON) on cell viability in human Jurkat T cells (clone E6.1). Exponentially growing Jurkat T cells (1 × 10 4 cells/well) were treated with increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. Cell viability was assessed by the MTT assay, reflecting the enzymatic reduction of tetrazolium dye in metabolically active cells. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) denote statistically significant differences compared to the vehicle control group ( p < 0.05).

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Effects of beauvericin (BEA), enniatin B (ENN B), and moniliformin (MON) on cell viability in human Jurkat T cells (clone E6.1). Exponentially growing Jurkat T cells (1 × 10 4 cells/well) were treated with increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. Cell viability was assessed by the MTT assay, reflecting the enzymatic reduction of tetrazolium dye in metabolically active cells. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) denote statistically significant differences compared to the vehicle control group ( p < 0.05).

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: MTT Assay, Metabolic Labelling, Control

    Comparative cytotoxic effects of combined mycotoxin treatments on human Jurkat T cells. Jurkat T cells were exposed to BEA in combination with ENN B (A) , BEA with MON (B) , and ENN B with MON (C) at the indicated concentrations for 24 h. Cell viability was determined using the MTT assay. All combinations induced a concentration-dependent decrease in cell viability, with combined treatments generally exhibiting greater cytotoxic effects than individual compounds. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) denote statistically significant differences compared to the vehicle control group ( p < 0.05).

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Comparative cytotoxic effects of combined mycotoxin treatments on human Jurkat T cells. Jurkat T cells were exposed to BEA in combination with ENN B (A) , BEA with MON (B) , and ENN B with MON (C) at the indicated concentrations for 24 h. Cell viability was determined using the MTT assay. All combinations induced a concentration-dependent decrease in cell viability, with combined treatments generally exhibiting greater cytotoxic effects than individual compounds. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) denote statistically significant differences compared to the vehicle control group ( p < 0.05).

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: MTT Assay, Concentration Assay, Control

    Combined cytotoxic effects of BEA, ENN B, and MON on human Jurkat T cells. Jurkat T cells were treated with BEA, ENN B, and MON individually and in combination (BEA + ENN B+ MON) at the indicated concentrations for 24 h. Cell viability was assessed using the MTT assay. The combined treatment exhibited a more pronounced reduction in cell viability compared to individual mycotoxins. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) denote statistically significant differences compared to the vehicle control group ( p < 0.05).

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Combined cytotoxic effects of BEA, ENN B, and MON on human Jurkat T cells. Jurkat T cells were treated with BEA, ENN B, and MON individually and in combination (BEA + ENN B+ MON) at the indicated concentrations for 24 h. Cell viability was assessed using the MTT assay. The combined treatment exhibited a more pronounced reduction in cell viability compared to individual mycotoxins. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) denote statistically significant differences compared to the vehicle control group ( p < 0.05).

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: MTT Assay, Control

    Dose–effect parameters of BEA, ENN B, and MON in human Jurkat T cells following combined treatments.

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Dose–effect parameters of BEA, ENN B, and MON in human Jurkat T cells following combined treatments.

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques:

    Combination index ( C I ) versus fraction affected ( F a ) curves for beauvericin (BEA), enniatin B (ENN B), and moniliformin (MON) in human Jurkat T cells. C I – F a plots were generated using the Chou–Talalay median-effect method for cells exposed to BEA + ENN B (A) , BEA + MON (B) , ENN B+ MON (C) , and the ternary mixture BEA + ENN B+ MON (D) for 24 h. Each data point represents the mean C I ± SD derived from three independent biological experiments ( n = 3 ) at specified fractional effect levels. The horizontal dashed line ( C I = 1 ) denotes additivity ( 0.90 ≤ C I ≤ 1.10 ); values below 0.90 ( C I < 0.90 ) represent synergism, whereas values above 1.10 ( C I > 1.10 ) indicate antagonism.

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Combination index ( C I ) versus fraction affected ( F a ) curves for beauvericin (BEA), enniatin B (ENN B), and moniliformin (MON) in human Jurkat T cells. C I – F a plots were generated using the Chou–Talalay median-effect method for cells exposed to BEA + ENN B (A) , BEA + MON (B) , ENN B+ MON (C) , and the ternary mixture BEA + ENN B+ MON (D) for 24 h. Each data point represents the mean C I ± SD derived from three independent biological experiments ( n = 3 ) at specified fractional effect levels. The horizontal dashed line ( C I = 1 ) denotes additivity ( 0.90 ≤ C I ≤ 1.10 ); values below 0.90 ( C I < 0.90 ) represent synergism, whereas values above 1.10 ( C I > 1.10 ) indicate antagonism.

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: Generated, Derivative Assay

    Combination index (CI) and dose‐reduction index (DRI) values for cytotoxic interactions of BEA, ENN B, and MON in human Jurkat T cells.

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Combination index (CI) and dose‐reduction index (DRI) values for cytotoxic interactions of BEA, ENN B, and MON in human Jurkat T cells.

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques:

    Polygonogram illustrating the interaction patterns among BEA, ENN B, and MON at a fractional effect of 0.5 (fa = 0.5) in human Jurkat T cells. Thick solid lines indicate synergistic interactions between toxin pairs, while the triangular connection represents synergism in the ternary combination. The results demonstrate consistent synergistic effects among all combinations at this effect level, supporting synergistic interactions under sub-maximal effect conditions based on Combination Index analysis.

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Polygonogram illustrating the interaction patterns among BEA, ENN B, and MON at a fractional effect of 0.5 (fa = 0.5) in human Jurkat T cells. Thick solid lines indicate synergistic interactions between toxin pairs, while the triangular connection represents synergism in the ternary combination. The results demonstrate consistent synergistic effects among all combinations at this effect level, supporting synergistic interactions under sub-maximal effect conditions based on Combination Index analysis.

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: Analysis

    Effects of BEA, ENN B, and MON on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU). Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Effects of BEA, ENN B, and MON on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA (0–7.24 μM), ENN B (0–17.88 μM), and MON (0–161.80 μM) for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU). Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: ROS Assay, Fluorescence, Control

    Effects of BEA, ENN B, and MON, individually and in combination, on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA, ENN B, and MON, alone or in binary and ternary combinations, for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU) (A) BEA + ENN B (B) BEA + MON (C) ENN B+ MON, and (D) BEA + ENN B+ MON. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

    Journal: Frontiers in Toxicology

    Article Title: Combined exposure to emerging Fusarium mycotoxins produces concentration-dependent synergistic toxicity in Jurkat T cells

    doi: 10.3389/ftox.2026.1924250

    Figure Lengend Snippet: Effects of BEA, ENN B, and MON, individually and in combination, on intracellular reactive oxygen species (ROS) generation in human Jurkat T cells. Cells were exposed to increasing concentrations of BEA, ENN B, and MON, alone or in binary and ternary combinations, for 24 h. ROS levels were measured using a Total ROS assay and expressed as relative fluorescence units (RFU) (A) BEA + ENN B (B) BEA + MON (C) ENN B+ MON, and (D) BEA + ENN B+ MON. Data represent Mean ± SD of three independent biological experiments (n = 3), with individual experimental values shown as overlayed data points. Asterisks (*) indicate statistically significant differences compared to the control group ( p < 0.05).

    Article Snippet: Human Jurkat T lymphocyte cells (catalog number: EP-CL-0129; Elabscience, Houston, TX, United States) were used as an experimental model in this study.

    Techniques: ROS Assay, Fluorescence, Control