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liver carcinoma hepg 2  (ATCC)


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    Structured Review

    ATCC liver carcinoma hepg 2
    The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards <t>the</t> <t>HepG-2</t> cells and control THLE-2 cells, normalized to Staurosporine as reference drug
    Liver Carcinoma Hepg 2, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 29071 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/liver carcinoma hepg 2/product/ATCC
    Average 99 stars, based on 29071 article reviews
    liver carcinoma hepg 2 - by Bioz Stars, 2026-05
    99/100 stars

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    1) Product Images from "Aspergillus flavus glutathione transferase as a potential approach for synthesis of epothilone-glutathione conjugates with enhanced anticancer activity for the drug-resistant cells: characterization and molecular docking analysis"

    Article Title: Aspergillus flavus glutathione transferase as a potential approach for synthesis of epothilone-glutathione conjugates with enhanced anticancer activity for the drug-resistant cells: characterization and molecular docking analysis

    Journal: BMC Microbiology

    doi: 10.1186/s12866-026-05037-0

    The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards the HepG-2 cells and control THLE-2 cells, normalized to Staurosporine as reference drug
    Figure Legend Snippet: The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards the HepG-2 cells and control THLE-2 cells, normalized to Staurosporine as reference drug

    Techniques Used: Activity Assay, Control



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    The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards <t>the</t> <t>HepG-2</t> cells and control THLE-2 cells, normalized to Staurosporine as reference drug
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    hepg 2  (ATCC)
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    The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards <t>the</t> <t>HepG-2</t> cells and control THLE-2 cells, normalized to Staurosporine as reference drug
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    ATCC hepg 2 cell line
    Apoptotic effects of black Vitis vinifera seed oil (BVVO) and its unsaponifiable fraction (UnSap), and their ameliorating effects on the expression of cell cycle-related genes <t>in</t> <t>HepG-2</t> cells, compared with those of 5-FU. (A) EC 100 values of BVVO and UnSap in peripheral blood mononuclear cells (PBMCs) compared with those of 5-FU. EC 100 , the concentration of the studied sample that caused 100% viability of the PBMCs. (B, C) The IC 50 and selectivity index (SI) values, respectively, of BVVO, UnSap, and 5-FU. The IC 50 , the inhibitory concentration of BVVO, UnSap, or 5-FU, caused 50% inhibition of cancer cell growth. The SI is determined by dividing the cytotoxic concentration (the concentration of the sample that inhibits 50% of the growth of normal viable cells) by the IC 50 value in cancer cells. (D) Percentage of caspase 3/7 activity in the HepG-2 cell line. (E) BCL-2 -associated X-protein
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    hepg  (ATCC)
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    Image Search Results


    The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards the HepG-2 cells and control THLE-2 cells, normalized to Staurosporine as reference drug

    Journal: BMC Microbiology

    Article Title: Aspergillus flavus glutathione transferase as a potential approach for synthesis of epothilone-glutathione conjugates with enhanced anticancer activity for the drug-resistant cells: characterization and molecular docking analysis

    doi: 10.1186/s12866-026-05037-0

    Figure Lengend Snippet: The antiproliferative activity of the epothilone and glutathione-Epothilone conjugates at 1:2 and 1: 4 M:M, towards the HepG-2 cells and control THLE-2 cells, normalized to Staurosporine as reference drug

    Article Snippet: The activity of constructed Glutathione-Epothilone B conjugate against the liver carcinoma (HepG-2) (ATCC HB-8065), and normal epithelial cells (THLE-2) (ATCC CRL-2706) was determined by the MTT reagent [ ].

    Techniques: Activity Assay, Control

    Apoptotic effects of black Vitis vinifera seed oil (BVVO) and its unsaponifiable fraction (UnSap), and their ameliorating effects on the expression of cell cycle-related genes in HepG-2 cells, compared with those of 5-FU. (A) EC 100 values of BVVO and UnSap in peripheral blood mononuclear cells (PBMCs) compared with those of 5-FU. EC 100 , the concentration of the studied sample that caused 100% viability of the PBMCs. (B, C) The IC 50 and selectivity index (SI) values, respectively, of BVVO, UnSap, and 5-FU. The IC 50 , the inhibitory concentration of BVVO, UnSap, or 5-FU, caused 50% inhibition of cancer cell growth. The SI is determined by dividing the cytotoxic concentration (the concentration of the sample that inhibits 50% of the growth of normal viable cells) by the IC 50 value in cancer cells. (D) Percentage of caspase 3/7 activity in the HepG-2 cell line. (E) BCL-2 -associated X-protein

    Journal: Scientific Reports

    Article Title: Unsaponifiable fraction of black Vitis vinifera seed oil attenuates liver cancer progression by targeting apoptosis and key tumor-associated genes: In vitro, in vivo, and in silico studies

    doi: 10.1038/s41598-026-44404-9

    Figure Lengend Snippet: Apoptotic effects of black Vitis vinifera seed oil (BVVO) and its unsaponifiable fraction (UnSap), and their ameliorating effects on the expression of cell cycle-related genes in HepG-2 cells, compared with those of 5-FU. (A) EC 100 values of BVVO and UnSap in peripheral blood mononuclear cells (PBMCs) compared with those of 5-FU. EC 100 , the concentration of the studied sample that caused 100% viability of the PBMCs. (B, C) The IC 50 and selectivity index (SI) values, respectively, of BVVO, UnSap, and 5-FU. The IC 50 , the inhibitory concentration of BVVO, UnSap, or 5-FU, caused 50% inhibition of cancer cell growth. The SI is determined by dividing the cytotoxic concentration (the concentration of the sample that inhibits 50% of the growth of normal viable cells) by the IC 50 value in cancer cells. (D) Percentage of caspase 3/7 activity in the HepG-2 cell line. (E) BCL-2 -associated X-protein " BAX ", retinoblastoma “ RB ” 1 , cyclin-dependent kinase inhibitor “ CDKN1A ”, and tumor protein “ TP53 ” fold expression. (F) E2 promoter binding factor “ E2F ” 4 , Kirsten rat sarcoma virus “ KRAS ”, B-cell lymphoma “ BCL ” 2 , and nuclear factor “ NF ” KB1 fold expression. The results are presented as the mean ± S.E. (n = 5), and significance was achieved at * p < 0.05, ** p < 0.01, and *** p < 0.0001. (*, black) indicates a comparison with the 5-FU; (*, red) refers to the comparison between the treatment with BVVO and UnSap.

    Article Snippet: The HepG-2 cell line was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Expressing, Concentration Assay, Inhibition, Activity Assay, Binding Assay, Virus, Comparison

    Heatmap plot and Ingenuity pathway analysis (IPA) network. (A) A heatmap showing the clustering of the expression of the investigated genes in HepG-2 cells. The color ranges from blue (low expression) to red (high expression). (B) QIAGEN IPA network of the proteins examined to evaluate the anticancer effects of the unsaponifiable fraction (UnSap) from black Vitis vinifera seed oil (BVVO) in comparison with 5-FU. Green denotes a significantly decreased level; red indicates a significantly increased level, according to color intensity. On the basis of the IPA database, molecular connections between interacting genes represent direct (solid line) or indirect (dotted line) functional links. The IPA legend describes the symbols representing the IPA networks provided in the inset.

    Journal: Scientific Reports

    Article Title: Unsaponifiable fraction of black Vitis vinifera seed oil attenuates liver cancer progression by targeting apoptosis and key tumor-associated genes: In vitro, in vivo, and in silico studies

    doi: 10.1038/s41598-026-44404-9

    Figure Lengend Snippet: Heatmap plot and Ingenuity pathway analysis (IPA) network. (A) A heatmap showing the clustering of the expression of the investigated genes in HepG-2 cells. The color ranges from blue (low expression) to red (high expression). (B) QIAGEN IPA network of the proteins examined to evaluate the anticancer effects of the unsaponifiable fraction (UnSap) from black Vitis vinifera seed oil (BVVO) in comparison with 5-FU. Green denotes a significantly decreased level; red indicates a significantly increased level, according to color intensity. On the basis of the IPA database, molecular connections between interacting genes represent direct (solid line) or indirect (dotted line) functional links. The IPA legend describes the symbols representing the IPA networks provided in the inset.

    Article Snippet: The HepG-2 cell line was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Expressing, Comparison, Functional Assay

    V-MOF membrane effectiveness, DOX@V-MOF membrane, (a) HePG-2 cell viability, (b) HePG-2 inhibitory (%), (c) MCF-7 cell viability, (d) inhibitory of MCF-7 (%).

    Journal: RSC Advances

    Article Title: Electrospun nanofiber membrane of chitosan/polyvinyl alcohol embedded with DOX-loaded V-MOFs for controlled drug release and multifunctional biological activity

    doi: 10.1039/d6ra01018k

    Figure Lengend Snippet: V-MOF membrane effectiveness, DOX@V-MOF membrane, (a) HePG-2 cell viability, (b) HePG-2 inhibitory (%), (c) MCF-7 cell viability, (d) inhibitory of MCF-7 (%).

    Article Snippet: The MCF-7 human breast cancer cell line and the HepG-2 human hepatocellular carcinoma cell line were obtained from the American Type Culture Collection (ATCC) in Rockville, Maryland, and were utilized in this investigation.

    Techniques: Membrane