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human liver epithelial cell line thle 2  (ATCC)


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    Structured Review

    ATCC human liver epithelial cell line thle 2
    Cell viability assays were conducted using the WST-1 method to evaluate the effects of valproic acid (VPA) and bempedoic acid (BA), alone or in combination, on the viability of <t>THLE-2,</t> Hep3B, and Huh7 cells. (A) The outlines of the WST-1 assay protocol were followed in the study. The effects of (B) valproic acid (0,1, and 2mM), (C) bempedoic acid (0,10, and 25μM), and (D) their combinations on THLE-2 cells, respectively. Similarly, (E–G) show the effects on Hep3B cells and (H–J) present corresponding data for Huh7 cells. Cell viability was measured at 72 and 96 hours post-treatment, as shown at the top of each plot. Red-highlighted values indicate fold change inhibitory effects compared to the control, where values less than one indicate inhibition and values greater than one represent stimulation. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns-non-significant. Analysis was performed using one-way ANOVA. Data are shown as mean ± SD.
    Human Liver Epithelial Cell Line Thle 2, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 652 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human liver epithelial cell line thle 2/product/ATCC
    Average 98 stars, based on 652 article reviews
    human liver epithelial cell line thle 2 - by Bioz Stars, 2026-05
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    1) Product Images from "Simultaneous Inhibition of ACLY and OGDH Has a Synergistic Effect on Hepatocellular Carcinoma Cell Lines"

    Article Title: Simultaneous Inhibition of ACLY and OGDH Has a Synergistic Effect on Hepatocellular Carcinoma Cell Lines

    Journal: bioRxiv

    doi: 10.64898/2026.04.19.716936

    Cell viability assays were conducted using the WST-1 method to evaluate the effects of valproic acid (VPA) and bempedoic acid (BA), alone or in combination, on the viability of THLE-2, Hep3B, and Huh7 cells. (A) The outlines of the WST-1 assay protocol were followed in the study. The effects of (B) valproic acid (0,1, and 2mM), (C) bempedoic acid (0,10, and 25μM), and (D) their combinations on THLE-2 cells, respectively. Similarly, (E–G) show the effects on Hep3B cells and (H–J) present corresponding data for Huh7 cells. Cell viability was measured at 72 and 96 hours post-treatment, as shown at the top of each plot. Red-highlighted values indicate fold change inhibitory effects compared to the control, where values less than one indicate inhibition and values greater than one represent stimulation. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns-non-significant. Analysis was performed using one-way ANOVA. Data are shown as mean ± SD.
    Figure Legend Snippet: Cell viability assays were conducted using the WST-1 method to evaluate the effects of valproic acid (VPA) and bempedoic acid (BA), alone or in combination, on the viability of THLE-2, Hep3B, and Huh7 cells. (A) The outlines of the WST-1 assay protocol were followed in the study. The effects of (B) valproic acid (0,1, and 2mM), (C) bempedoic acid (0,10, and 25μM), and (D) their combinations on THLE-2 cells, respectively. Similarly, (E–G) show the effects on Hep3B cells and (H–J) present corresponding data for Huh7 cells. Cell viability was measured at 72 and 96 hours post-treatment, as shown at the top of each plot. Red-highlighted values indicate fold change inhibitory effects compared to the control, where values less than one indicate inhibition and values greater than one represent stimulation. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns-non-significant. Analysis was performed using one-way ANOVA. Data are shown as mean ± SD.

    Techniques Used: WST-1 Assay, Control, Inhibition



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    Image Search Results


    Cell viability assays were conducted using the WST-1 method to evaluate the effects of valproic acid (VPA) and bempedoic acid (BA), alone or in combination, on the viability of THLE-2, Hep3B, and Huh7 cells. (A) The outlines of the WST-1 assay protocol were followed in the study. The effects of (B) valproic acid (0,1, and 2mM), (C) bempedoic acid (0,10, and 25μM), and (D) their combinations on THLE-2 cells, respectively. Similarly, (E–G) show the effects on Hep3B cells and (H–J) present corresponding data for Huh7 cells. Cell viability was measured at 72 and 96 hours post-treatment, as shown at the top of each plot. Red-highlighted values indicate fold change inhibitory effects compared to the control, where values less than one indicate inhibition and values greater than one represent stimulation. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns-non-significant. Analysis was performed using one-way ANOVA. Data are shown as mean ± SD.

    Journal: bioRxiv

    Article Title: Simultaneous Inhibition of ACLY and OGDH Has a Synergistic Effect on Hepatocellular Carcinoma Cell Lines

    doi: 10.64898/2026.04.19.716936

    Figure Lengend Snippet: Cell viability assays were conducted using the WST-1 method to evaluate the effects of valproic acid (VPA) and bempedoic acid (BA), alone or in combination, on the viability of THLE-2, Hep3B, and Huh7 cells. (A) The outlines of the WST-1 assay protocol were followed in the study. The effects of (B) valproic acid (0,1, and 2mM), (C) bempedoic acid (0,10, and 25μM), and (D) their combinations on THLE-2 cells, respectively. Similarly, (E–G) show the effects on Hep3B cells and (H–J) present corresponding data for Huh7 cells. Cell viability was measured at 72 and 96 hours post-treatment, as shown at the top of each plot. Red-highlighted values indicate fold change inhibitory effects compared to the control, where values less than one indicate inhibition and values greater than one represent stimulation. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001, ns-non-significant. Analysis was performed using one-way ANOVA. Data are shown as mean ± SD.

    Article Snippet: The immortalized human liver epithelial cell line THLE-2 and human HCC cell lines Hep3B were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: WST-1 Assay, Control, Inhibition