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human liver cancer cell line hepg2  (ATCC)


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    ATCC human liver cancer cell line hepg2
    Fluorescent microscopy analysis of <t>HepG2</t> cells treated with synthetic compounds (4–6a,b) and stained with acridine orange/ethidium bromide (AO/EB).
    Human Liver Cancer Cell Line Hepg2, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 31283 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human liver cancer cell line hepg2/product/ATCC
    Average 99 stars, based on 31283 article reviews
    human liver cancer cell line hepg2 - by Bioz Stars, 2026-02
    99/100 stars

    Images

    1) Product Images from "Novel diazenyl chalcones with a 2-arylidene hydrazineylidene thiazole moiety: synthesis, anticancer potential, spectroscopic characterisation, and molecular docking studies"

    Article Title: Novel diazenyl chalcones with a 2-arylidene hydrazineylidene thiazole moiety: synthesis, anticancer potential, spectroscopic characterisation, and molecular docking studies

    Journal: RSC Advances

    doi: 10.1039/d5ra07769a

    Fluorescent microscopy analysis of HepG2 cells treated with synthetic compounds (4–6a,b) and stained with acridine orange/ethidium bromide (AO/EB).
    Figure Legend Snippet: Fluorescent microscopy analysis of HepG2 cells treated with synthetic compounds (4–6a,b) and stained with acridine orange/ethidium bromide (AO/EB).

    Techniques Used: Microscopy, Staining

    (A) Microscopic view of the cell migration inhibition assay of the HepG2 cell line after 48 hours. (B) Quantitative analysis of the wound area by calculating the wound closure percentage and migration rate after 48 hours, compared to the initial time (0 hours). (C) Relative fold change in the gene expression of MMP-2 and MMP-9 in cells treated with synthetic compounds (4–6a,b) in HepG-2. All assays were conducted in triplicate, and the results are expressed as mean ± SEM. MMP: matrix metalloproteinase.
    Figure Legend Snippet: (A) Microscopic view of the cell migration inhibition assay of the HepG2 cell line after 48 hours. (B) Quantitative analysis of the wound area by calculating the wound closure percentage and migration rate after 48 hours, compared to the initial time (0 hours). (C) Relative fold change in the gene expression of MMP-2 and MMP-9 in cells treated with synthetic compounds (4–6a,b) in HepG-2. All assays were conducted in triplicate, and the results are expressed as mean ± SEM. MMP: matrix metalloproteinase.

    Techniques Used: Migration, Inhibition, Gene Expression

    Structure–activity relationship (SAR) of the synthesised azo derivatives (4–6a,b) showing the effect of aromatic substitution on cytotoxic selectivity. Selectivity index (SI) values against MDA-MB-231 and HepG2 cells relative to WI-38 normal cells are shown.
    Figure Legend Snippet: Structure–activity relationship (SAR) of the synthesised azo derivatives (4–6a,b) showing the effect of aromatic substitution on cytotoxic selectivity. Selectivity index (SI) values against MDA-MB-231 and HepG2 cells relative to WI-38 normal cells are shown.

    Techniques Used: Activity Assay



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    Image Search Results


    Fluorescent microscopy analysis of HepG2 cells treated with synthetic compounds (4–6a,b) and stained with acridine orange/ethidium bromide (AO/EB).

    Journal: RSC Advances

    Article Title: Novel diazenyl chalcones with a 2-arylidene hydrazineylidene thiazole moiety: synthesis, anticancer potential, spectroscopic characterisation, and molecular docking studies

    doi: 10.1039/d5ra07769a

    Figure Lengend Snippet: Fluorescent microscopy analysis of HepG2 cells treated with synthetic compounds (4–6a,b) and stained with acridine orange/ethidium bromide (AO/EB).

    Article Snippet: Normal human skin fibroblasts (HSF), the human breast cancer epithelial cell line (MDA), and the human liver cancer cell line (HepG2) were purchased from VACCERA Egypt and obtained from the American Type Culture Collection (ATCC).

    Techniques: Microscopy, Staining

    (A) Microscopic view of the cell migration inhibition assay of the HepG2 cell line after 48 hours. (B) Quantitative analysis of the wound area by calculating the wound closure percentage and migration rate after 48 hours, compared to the initial time (0 hours). (C) Relative fold change in the gene expression of MMP-2 and MMP-9 in cells treated with synthetic compounds (4–6a,b) in HepG-2. All assays were conducted in triplicate, and the results are expressed as mean ± SEM. MMP: matrix metalloproteinase.

    Journal: RSC Advances

    Article Title: Novel diazenyl chalcones with a 2-arylidene hydrazineylidene thiazole moiety: synthesis, anticancer potential, spectroscopic characterisation, and molecular docking studies

    doi: 10.1039/d5ra07769a

    Figure Lengend Snippet: (A) Microscopic view of the cell migration inhibition assay of the HepG2 cell line after 48 hours. (B) Quantitative analysis of the wound area by calculating the wound closure percentage and migration rate after 48 hours, compared to the initial time (0 hours). (C) Relative fold change in the gene expression of MMP-2 and MMP-9 in cells treated with synthetic compounds (4–6a,b) in HepG-2. All assays were conducted in triplicate, and the results are expressed as mean ± SEM. MMP: matrix metalloproteinase.

    Article Snippet: Normal human skin fibroblasts (HSF), the human breast cancer epithelial cell line (MDA), and the human liver cancer cell line (HepG2) were purchased from VACCERA Egypt and obtained from the American Type Culture Collection (ATCC).

    Techniques: Migration, Inhibition, Gene Expression

    Structure–activity relationship (SAR) of the synthesised azo derivatives (4–6a,b) showing the effect of aromatic substitution on cytotoxic selectivity. Selectivity index (SI) values against MDA-MB-231 and HepG2 cells relative to WI-38 normal cells are shown.

    Journal: RSC Advances

    Article Title: Novel diazenyl chalcones with a 2-arylidene hydrazineylidene thiazole moiety: synthesis, anticancer potential, spectroscopic characterisation, and molecular docking studies

    doi: 10.1039/d5ra07769a

    Figure Lengend Snippet: Structure–activity relationship (SAR) of the synthesised azo derivatives (4–6a,b) showing the effect of aromatic substitution on cytotoxic selectivity. Selectivity index (SI) values against MDA-MB-231 and HepG2 cells relative to WI-38 normal cells are shown.

    Article Snippet: Normal human skin fibroblasts (HSF), the human breast cancer epithelial cell line (MDA), and the human liver cancer cell line (HepG2) were purchased from VACCERA Egypt and obtained from the American Type Culture Collection (ATCC).

    Techniques: Activity Assay