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cell lines hmc3 human microglial cell line atcc crl 3304 bt0309 mouse brain tumor  (ATCC)


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    ATCC cell lines hmc3 human microglial cell line atcc crl 3304 bt0309 mouse brain tumor
    Cell Lines Hmc3 Human Microglial Cell Line Atcc Crl 3304 Bt0309 Mouse Brain Tumor, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 763 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cell lines hmc3 human microglial cell line atcc crl 3304 bt0309 mouse brain tumor/product/ATCC
    Average 99 stars, based on 763 article reviews
    cell lines hmc3 human microglial cell line atcc crl 3304 bt0309 mouse brain tumor - by Bioz Stars, 2026-03
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    ATCC cell lines hmc3 human microglial cell line atcc crl 3304 bt0309 mouse brain tumor
    Cell Lines Hmc3 Human Microglial Cell Line Atcc Crl 3304 Bt0309 Mouse Brain Tumor, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Genecopoeia 1321n1 human astrocytoma cell line
    JAK1 and PERK are required to augment TNF‐α induced gene expression in human glioma cells. (A) <t>1321N1</t> cells stably expressing Cas9 were transfected with non‐targeting (NT) or JAK1 guide RNAs (gRNA) to establish non‐clonal cell lines. These cells were then treated with IFN‐γ (10 ng/mL) for 30 min followed by immunoblotting. (B) NT and JAK1 gRNA (#2) cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. (C) 1321N1 cells stably expressing Cas9 were transfected with NT or PERK gRNA to establish non‐clonal cell lines. These cells were then treated with thaps (1 μM) for the indicated times followed by immunoblotting. (D) NT and PERK gRNA cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. N = 4, data are means ± standard deviation.
    1321n1 Human Astrocytoma Cell Line, supplied by Genecopoeia, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human brain tumor cell line
    JAK1 and PERK are required to augment TNF‐α induced gene expression in human glioma cells. (A) <t>1321N1</t> cells stably expressing Cas9 were transfected with non‐targeting (NT) or JAK1 guide RNAs (gRNA) to establish non‐clonal cell lines. These cells were then treated with IFN‐γ (10 ng/mL) for 30 min followed by immunoblotting. (B) NT and JAK1 gRNA (#2) cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. (C) 1321N1 cells stably expressing Cas9 were transfected with NT or PERK gRNA to establish non‐clonal cell lines. These cells were then treated with thaps (1 μM) for the indicated times followed by immunoblotting. (D) NT and PERK gRNA cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. N = 4, data are means ± standard deviation.
    Human Brain Tumor Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human tumor brain cell line u87
    Anti-proliferative potential of 7-Lut and 8-Lut tested on human tumor glial cell line <t>U87,</t> by MTS assay. ( A , B ) cell viability after 24 h of exposure to 7-Lut and 8-Lut. ( C , D ) cell viability after 48 h of exposure to 7-Lut and 8-Lut. ( n = 3). Notation (*) means results without statistical significance ( p > 0.05); (**) means results with statistical significance (0.05 < p < 0.01); (***) means results with high statistical significance ( p < 0.01); 7-Lut means luteolin-7- O -glucoside; 8-Lut means luteolin-8- C -glucoside; MTS means 3-(4,5-dimethyl-thiazol-2-yl)-5-(3-carboxy-methoxy- phenyl)-2 -(4-sulfophenyl)-2H-tetrazolium (MTS).
    Human Tumor Brain Cell Line U87, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human tumor brain cell line u87/product/ATCC
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    Pasteur Institute human brain tumor cell line u-251
    Anti-proliferative potential of 7-Lut and 8-Lut tested on human tumor glial cell line <t>U87,</t> by MTS assay. ( A , B ) cell viability after 24 h of exposure to 7-Lut and 8-Lut. ( C , D ) cell viability after 48 h of exposure to 7-Lut and 8-Lut. ( n = 3). Notation (*) means results without statistical significance ( p > 0.05); (**) means results with statistical significance (0.05 < p < 0.01); (***) means results with high statistical significance ( p < 0.01); 7-Lut means luteolin-7- O -glucoside; 8-Lut means luteolin-8- C -glucoside; MTS means 3-(4,5-dimethyl-thiazol-2-yl)-5-(3-carboxy-methoxy- phenyl)-2 -(4-sulfophenyl)-2H-tetrazolium (MTS).
    Human Brain Tumor Cell Line U 251, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human tumor brain cell line u87 mg
    Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human normal brain cell line NHA and human tumor brain cell line <t>U87,</t> in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 24 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).
    Human Tumor Brain Cell Line U87 Mg, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC human brain tumor cell lines
    Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human normal brain cell line NHA and human tumor brain cell line <t>U87,</t> in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 24 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).
    Human Brain Tumor Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human brain tumor cell lines/product/ATCC
    Average 99 stars, based on 1 article reviews
    human brain tumor cell lines - by Bioz Stars, 2026-03
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    ATCC human brain tumor cell line u87
    Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human normal brain cell line NHA and human tumor brain cell line <t>U87,</t> in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 24 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).
    Human Brain Tumor Cell Line U87, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human brain tumor cell line u87/product/ATCC
    Average 99 stars, based on 1 article reviews
    human brain tumor cell line u87 - by Bioz Stars, 2026-03
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    JAK1 and PERK are required to augment TNF‐α induced gene expression in human glioma cells. (A) 1321N1 cells stably expressing Cas9 were transfected with non‐targeting (NT) or JAK1 guide RNAs (gRNA) to establish non‐clonal cell lines. These cells were then treated with IFN‐γ (10 ng/mL) for 30 min followed by immunoblotting. (B) NT and JAK1 gRNA (#2) cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. (C) 1321N1 cells stably expressing Cas9 were transfected with NT or PERK gRNA to establish non‐clonal cell lines. These cells were then treated with thaps (1 μM) for the indicated times followed by immunoblotting. (D) NT and PERK gRNA cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. N = 4, data are means ± standard deviation.

    Journal: Glia

    Article Title: Endoplasmic Reticulum Stress Amplifies Cytokine Responses in Astrocytes via a PERK / eIF2α / JAK1 Signaling Axis

    doi: 10.1002/glia.70067

    Figure Lengend Snippet: JAK1 and PERK are required to augment TNF‐α induced gene expression in human glioma cells. (A) 1321N1 cells stably expressing Cas9 were transfected with non‐targeting (NT) or JAK1 guide RNAs (gRNA) to establish non‐clonal cell lines. These cells were then treated with IFN‐γ (10 ng/mL) for 30 min followed by immunoblotting. (B) NT and JAK1 gRNA (#2) cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. (C) 1321N1 cells stably expressing Cas9 were transfected with NT or PERK gRNA to establish non‐clonal cell lines. These cells were then treated with thaps (1 μM) for the indicated times followed by immunoblotting. (D) NT and PERK gRNA cells were treated with thaps (1 μM), TNF‐α (10 ng/mL), or both for 4 h followed by qPCR. N = 4, data are means ± standard deviation.

    Article Snippet: 1321N1 human astrocytoma cell line stably expressing Cas9 nuclease was purchased from GeneCopoeia.

    Techniques: Gene Expression, Stable Transfection, Expressing, Transfection, Western Blot, Standard Deviation

    Anti-proliferative potential of 7-Lut and 8-Lut tested on human tumor glial cell line U87, by MTS assay. ( A , B ) cell viability after 24 h of exposure to 7-Lut and 8-Lut. ( C , D ) cell viability after 48 h of exposure to 7-Lut and 8-Lut. ( n = 3). Notation (*) means results without statistical significance ( p > 0.05); (**) means results with statistical significance (0.05 < p < 0.01); (***) means results with high statistical significance ( p < 0.01); 7-Lut means luteolin-7- O -glucoside; 8-Lut means luteolin-8- C -glucoside; MTS means 3-(4,5-dimethyl-thiazol-2-yl)-5-(3-carboxy-methoxy- phenyl)-2 -(4-sulfophenyl)-2H-tetrazolium (MTS).

    Journal: International Journal of Molecular Sciences

    Article Title: Anti-Proliferative Potential of Cynaroside and Orientin—In Silico (DYRK2) and In Vitro (U87 and Caco-2) Studies

    doi: 10.3390/ijms242316555

    Figure Lengend Snippet: Anti-proliferative potential of 7-Lut and 8-Lut tested on human tumor glial cell line U87, by MTS assay. ( A , B ) cell viability after 24 h of exposure to 7-Lut and 8-Lut. ( C , D ) cell viability after 48 h of exposure to 7-Lut and 8-Lut. ( n = 3). Notation (*) means results without statistical significance ( p > 0.05); (**) means results with statistical significance (0.05 < p < 0.01); (***) means results with high statistical significance ( p < 0.01); 7-Lut means luteolin-7- O -glucoside; 8-Lut means luteolin-8- C -glucoside; MTS means 3-(4,5-dimethyl-thiazol-2-yl)-5-(3-carboxy-methoxy- phenyl)-2 -(4-sulfophenyl)-2H-tetrazolium (MTS).

    Article Snippet: The cell lines investigated were the human tumor brain cell line U87 MG(ATCC-HTB-14) and the human colorectal carcinoma Caco-2 cells (ATCC, HTB-37).

    Techniques: MTS Assay

    The viability response of U87 cells to 7-Lut and 8-Lut after 24 and 48 h of exposure.

    Journal: International Journal of Molecular Sciences

    Article Title: Anti-Proliferative Potential of Cynaroside and Orientin—In Silico (DYRK2) and In Vitro (U87 and Caco-2) Studies

    doi: 10.3390/ijms242316555

    Figure Lengend Snippet: The viability response of U87 cells to 7-Lut and 8-Lut after 24 and 48 h of exposure.

    Article Snippet: The cell lines investigated were the human tumor brain cell line U87 MG(ATCC-HTB-14) and the human colorectal carcinoma Caco-2 cells (ATCC, HTB-37).

    Techniques:

    Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human normal brain cell line NHA and human tumor brain cell line U87, in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 24 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).

    Journal: International Journal of Molecular Sciences

    Article Title: Potential Benefits of Dietary Plant Compounds on Normal and Tumor Brain Cells in Humans: In Silico and In Vitro Approaches

    doi: 10.3390/ijms24087404

    Figure Lengend Snippet: Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human normal brain cell line NHA and human tumor brain cell line U87, in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 24 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).

    Article Snippet: Accordingly, MTS tests were performed on human normal brain cell line NHA (CC-2565, Lonza, Basel, Switzerland) and human tumor brain cell line U87 MG (ATCC-HTB-14, Tell City, IN, USA).

    Techniques: MTS Assay

    Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human tumor brain cell line U87, in anti-proliferative MTS assay. ( A ) U87 cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 48 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).

    Journal: International Journal of Molecular Sciences

    Article Title: Potential Benefits of Dietary Plant Compounds on Normal and Tumor Brain Cells in Humans: In Silico and In Vitro Approaches

    doi: 10.3390/ijms24087404

    Figure Lengend Snippet: Effect of test reference compounds (caffeic acid, gentisic acid, ferulic acid and para-aminobenzoic acid/PABA) on human tumor brain cell line U87, in anti-proliferative MTS assay. ( A ) U87 cell line viability after 24 h of exposure to test reference compounds. ( B ) U87 cell line viability after 48 h of exposure to test reference compounds. Data were the mean of three replicates (n = 3). Note: * = results without statistical significance ( p > 0.05); ** = results with statistical significance ( p < 0.05).

    Article Snippet: Accordingly, MTS tests were performed on human normal brain cell line NHA (CC-2565, Lonza, Basel, Switzerland) and human tumor brain cell line U87 MG (ATCC-HTB-14, Tell City, IN, USA).

    Techniques: MTS Assay

    Effect of crude ethanolic extract from fresh Anemone nemorosa L. plant material (AN1) on human normal brain cell line NHA and human tumor brain cell line U87, in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test vegetal extract AN1. ( B ) U87 cell line viability after 24 h of exposure to test vegetal extract AN1. All determinations were made in triplicate series, and the results are calculated as an average. Graphs A and B also present the percentage of cell viability by comparison to negative control series (CN). According to the statistical calculation, the results of the NHA and U87 cell lines in the cytotoxicity experiment were not statistically significant ( p > 0.05, n = 3).

    Journal: International Journal of Molecular Sciences

    Article Title: Potential Benefits of Dietary Plant Compounds on Normal and Tumor Brain Cells in Humans: In Silico and In Vitro Approaches

    doi: 10.3390/ijms24087404

    Figure Lengend Snippet: Effect of crude ethanolic extract from fresh Anemone nemorosa L. plant material (AN1) on human normal brain cell line NHA and human tumor brain cell line U87, in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test vegetal extract AN1. ( B ) U87 cell line viability after 24 h of exposure to test vegetal extract AN1. All determinations were made in triplicate series, and the results are calculated as an average. Graphs A and B also present the percentage of cell viability by comparison to negative control series (CN). According to the statistical calculation, the results of the NHA and U87 cell lines in the cytotoxicity experiment were not statistically significant ( p > 0.05, n = 3).

    Article Snippet: Accordingly, MTS tests were performed on human normal brain cell line NHA (CC-2565, Lonza, Basel, Switzerland) and human tumor brain cell line U87 MG (ATCC-HTB-14, Tell City, IN, USA).

    Techniques: MTS Assay, Comparison, Negative Control

    Effect of crude ethanolic extract from fresh Anemone nemorosa L. plant material (AN1) on human tumor brain cell line U87, in anti-proliferative MTS assay. ( A ) U87 cell line viability after 24 h of exposure to test vegetal extract AN1; ( B ) U87 cell line viability after 48 h of exposure to test vegetal extract AN1. All determinations were made in triplicate series, and the results are calculated as an average. The graphs present the percentage of the cell viability in series by comparison to positive control sample (CP) series. According to statistical calculation, the results on the U87 cells at 24 h and 48 h were not statistically significant ( p > 0.05).

    Journal: International Journal of Molecular Sciences

    Article Title: Potential Benefits of Dietary Plant Compounds on Normal and Tumor Brain Cells in Humans: In Silico and In Vitro Approaches

    doi: 10.3390/ijms24087404

    Figure Lengend Snippet: Effect of crude ethanolic extract from fresh Anemone nemorosa L. plant material (AN1) on human tumor brain cell line U87, in anti-proliferative MTS assay. ( A ) U87 cell line viability after 24 h of exposure to test vegetal extract AN1; ( B ) U87 cell line viability after 48 h of exposure to test vegetal extract AN1. All determinations were made in triplicate series, and the results are calculated as an average. The graphs present the percentage of the cell viability in series by comparison to positive control sample (CP) series. According to statistical calculation, the results on the U87 cells at 24 h and 48 h were not statistically significant ( p > 0.05).

    Article Snippet: Accordingly, MTS tests were performed on human normal brain cell line NHA (CC-2565, Lonza, Basel, Switzerland) and human tumor brain cell line U87 MG (ATCC-HTB-14, Tell City, IN, USA).

    Techniques: MTS Assay, Comparison, Positive Control

    Effect of hot ethanolic extract from dried Anemone nemorosa L. plant material (AN2) on human normal brain cell line NHA and human tumor brain cell line U87, in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test vegetal extract AN2. ( B ) U87 cell line viability after 24 h of exposure to test vegetal extract AN2. All determinations were made in triplicate series, and the results are calculated as an average. The graphs present the percentage of cell viability in each dilution point series by comparison to negative control point series (CN). By statistical calculation, the results on the NHA cell line were not statistically significant ( p > 0.05, n = 3), while the results on the U87 cell lines were statistically significant ( p < 0.05, n = 3).

    Journal: International Journal of Molecular Sciences

    Article Title: Potential Benefits of Dietary Plant Compounds on Normal and Tumor Brain Cells in Humans: In Silico and In Vitro Approaches

    doi: 10.3390/ijms24087404

    Figure Lengend Snippet: Effect of hot ethanolic extract from dried Anemone nemorosa L. plant material (AN2) on human normal brain cell line NHA and human tumor brain cell line U87, in cytotoxicity MTS assay. ( A ) NHA cell line viability after 24 h of exposure to test vegetal extract AN2. ( B ) U87 cell line viability after 24 h of exposure to test vegetal extract AN2. All determinations were made in triplicate series, and the results are calculated as an average. The graphs present the percentage of cell viability in each dilution point series by comparison to negative control point series (CN). By statistical calculation, the results on the NHA cell line were not statistically significant ( p > 0.05, n = 3), while the results on the U87 cell lines were statistically significant ( p < 0.05, n = 3).

    Article Snippet: Accordingly, MTS tests were performed on human normal brain cell line NHA (CC-2565, Lonza, Basel, Switzerland) and human tumor brain cell line U87 MG (ATCC-HTB-14, Tell City, IN, USA).

    Techniques: MTS Assay, Comparison, Negative Control

    Effect of hot ethanolic extract from dried Anemone nemorosa L. plant material (AN2) on human tumor brain cell line U87, in anti-proliferative MTS assay. ( A ) U87 cell line viability after 24 h of exposure to test vegetal extract AN2. ( B ) U87 cell line viability after 48 h exposure to test vegetal extract AN2. All determinations were made in triplicate series, and the results are calculated as an average. The graphs present the percentage of cell viability in each dilution point series by comparison to negative control point series (CN). By statistical calculation, the results on the U87 after 24 h of exposure to AN2 are statistically significant ( p < 0.05, n = 3), while the results at 48 h were not statistically significant ( p > 0.05, n = 3).

    Journal: International Journal of Molecular Sciences

    Article Title: Potential Benefits of Dietary Plant Compounds on Normal and Tumor Brain Cells in Humans: In Silico and In Vitro Approaches

    doi: 10.3390/ijms24087404

    Figure Lengend Snippet: Effect of hot ethanolic extract from dried Anemone nemorosa L. plant material (AN2) on human tumor brain cell line U87, in anti-proliferative MTS assay. ( A ) U87 cell line viability after 24 h of exposure to test vegetal extract AN2. ( B ) U87 cell line viability after 48 h exposure to test vegetal extract AN2. All determinations were made in triplicate series, and the results are calculated as an average. The graphs present the percentage of cell viability in each dilution point series by comparison to negative control point series (CN). By statistical calculation, the results on the U87 after 24 h of exposure to AN2 are statistically significant ( p < 0.05, n = 3), while the results at 48 h were not statistically significant ( p > 0.05, n = 3).

    Article Snippet: Accordingly, MTS tests were performed on human normal brain cell line NHA (CC-2565, Lonza, Basel, Switzerland) and human tumor brain cell line U87 MG (ATCC-HTB-14, Tell City, IN, USA).

    Techniques: MTS Assay, Comparison, Negative Control