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breast tumor cell lines skbr3  (ATCC)


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    ATCC breast tumor cell lines skbr3
    Antitumor activity of Brotheas amazonicus scorpion crude venom. MCF10A, <t>SKBR3,</t> MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with venom concentrations of 2, 10, 50, and 250 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.
    Breast Tumor Cell Lines Skbr3, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 6464 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/breast tumor cell lines skbr3/product/ATCC
    Average 99 stars, based on 6464 article reviews
    breast tumor cell lines skbr3 - by Bioz Stars, 2026-06
    99/100 stars

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    1) Product Images from "A novel scorpine-like peptide from the amazonian scorpion Brotheas amazonicus with cytolytic activity"

    Article Title: A novel scorpine-like peptide from the amazonian scorpion Brotheas amazonicus with cytolytic activity

    Journal: Frontiers in Pharmacology

    doi: 10.3389/fphar.2025.1652614

    Antitumor activity of Brotheas amazonicus scorpion crude venom. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with venom concentrations of 2, 10, 50, and 250 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.
    Figure Legend Snippet: Antitumor activity of Brotheas amazonicus scorpion crude venom. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with venom concentrations of 2, 10, 50, and 250 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Techniques Used: Activity Assay, Incubation, MTT Assay, Negative Control, Positive Control

    Antitumor activity of fractions from BamazV separated by molecular weight. Fractions were separated through an ultrafiltration process using a regenerated cellulose membrane (Amicon ® Ultra-15 Centrifugal Filter Ultracel ® 10K and 3K). MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazV fractions (<3 kDa, 3–10 kDa, and >10 kDa) at concentrations of 0.2, 1, 5, and 25 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 3 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.
    Figure Legend Snippet: Antitumor activity of fractions from BamazV separated by molecular weight. Fractions were separated through an ultrafiltration process using a regenerated cellulose membrane (Amicon ® Ultra-15 Centrifugal Filter Ultracel ® 10K and 3K). MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazV fractions (<3 kDa, 3–10 kDa, and >10 kDa) at concentrations of 0.2, 1, 5, and 25 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 3 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Techniques Used: Activity Assay, Molecular Weight, Membrane, Incubation, MTT Assay, Negative Control, Positive Control

    Antitumor activity of FPLC peaks from Bamaz>10 fraction. Peaks P31, P59, P75 and P81 were tested for antitumor effects in breast cancer cell lines. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with the indicated doses (see graphs) for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.
    Figure Legend Snippet: Antitumor activity of FPLC peaks from Bamaz>10 fraction. Peaks P31, P59, P75 and P81 were tested for antitumor effects in breast cancer cell lines. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with the indicated doses (see graphs) for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Techniques Used: Activity Assay, Incubation, MTT Assay, Negative Control, Positive Control

    Viability assay and type of cell death after treatment with the scorpine-like peptide. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazScplp1 (50 μg/mL) or controls (NC: culture medium; PC: 30% DMSO) for 24 h. From left to right, cell viability was assessed using the MTT assay. Representative flow cytometry dot plots (NC vs. BamazScplp1-treated cells) and quantification of apoptotic and necrotic cell death after treatment. Data represent the mean ± SD of triplicate measurements from 1 experiment. NC - negative control (only culture medium). Statistical significance: group vs. NC, * p < 0.05.
    Figure Legend Snippet: Viability assay and type of cell death after treatment with the scorpine-like peptide. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazScplp1 (50 μg/mL) or controls (NC: culture medium; PC: 30% DMSO) for 24 h. From left to right, cell viability was assessed using the MTT assay. Representative flow cytometry dot plots (NC vs. BamazScplp1-treated cells) and quantification of apoptotic and necrotic cell death after treatment. Data represent the mean ± SD of triplicate measurements from 1 experiment. NC - negative control (only culture medium). Statistical significance: group vs. NC, * p < 0.05.

    Techniques Used: Viability Assay, Incubation, MTT Assay, Flow Cytometry, Negative Control



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    Antitumor activity of Brotheas amazonicus scorpion crude venom. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with venom concentrations of 2, 10, 50, and 250 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Journal: Frontiers in Pharmacology

    Article Title: A novel scorpine-like peptide from the amazonian scorpion Brotheas amazonicus with cytolytic activity

    doi: 10.3389/fphar.2025.1652614

    Figure Lengend Snippet: Antitumor activity of Brotheas amazonicus scorpion crude venom. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with venom concentrations of 2, 10, 50, and 250 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Article Snippet: The breast tumor cell lines SKBr3, MCF-7, and MDA-MB-231, as well as the control breast epithelial cell line MCF10A, were obtained from the American Type Culture Collection (ATCC, Manassas, VA) and maintained in RPMI 1640 (Roswell Park Memorial Institute) supplemented with 10% FBS and 1% penicillin/streptomycin at 37 C, 5% CO 2 .

    Techniques: Activity Assay, Incubation, MTT Assay, Negative Control, Positive Control

    Antitumor activity of fractions from BamazV separated by molecular weight. Fractions were separated through an ultrafiltration process using a regenerated cellulose membrane (Amicon ® Ultra-15 Centrifugal Filter Ultracel ® 10K and 3K). MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazV fractions (<3 kDa, 3–10 kDa, and >10 kDa) at concentrations of 0.2, 1, 5, and 25 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 3 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Journal: Frontiers in Pharmacology

    Article Title: A novel scorpine-like peptide from the amazonian scorpion Brotheas amazonicus with cytolytic activity

    doi: 10.3389/fphar.2025.1652614

    Figure Lengend Snippet: Antitumor activity of fractions from BamazV separated by molecular weight. Fractions were separated through an ultrafiltration process using a regenerated cellulose membrane (Amicon ® Ultra-15 Centrifugal Filter Ultracel ® 10K and 3K). MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazV fractions (<3 kDa, 3–10 kDa, and >10 kDa) at concentrations of 0.2, 1, 5, and 25 μg/mL for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 3 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Article Snippet: The breast tumor cell lines SKBr3, MCF-7, and MDA-MB-231, as well as the control breast epithelial cell line MCF10A, were obtained from the American Type Culture Collection (ATCC, Manassas, VA) and maintained in RPMI 1640 (Roswell Park Memorial Institute) supplemented with 10% FBS and 1% penicillin/streptomycin at 37 C, 5% CO 2 .

    Techniques: Activity Assay, Molecular Weight, Membrane, Incubation, MTT Assay, Negative Control, Positive Control

    Antitumor activity of FPLC peaks from Bamaz>10 fraction. Peaks P31, P59, P75 and P81 were tested for antitumor effects in breast cancer cell lines. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with the indicated doses (see graphs) for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Journal: Frontiers in Pharmacology

    Article Title: A novel scorpine-like peptide from the amazonian scorpion Brotheas amazonicus with cytolytic activity

    doi: 10.3389/fphar.2025.1652614

    Figure Lengend Snippet: Antitumor activity of FPLC peaks from Bamaz>10 fraction. Peaks P31, P59, P75 and P81 were tested for antitumor effects in breast cancer cell lines. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with the indicated doses (see graphs) for 24 h. Then, cell viability was assessed using the MTT assay. Data represent the mean ± SD of triplicate measurements from 4 independent experiments. NC - negative control (only culture medium). PC - positive control (30% DMSO). Statistical significance: group vs. NC, * p < 0.05.

    Article Snippet: The breast tumor cell lines SKBr3, MCF-7, and MDA-MB-231, as well as the control breast epithelial cell line MCF10A, were obtained from the American Type Culture Collection (ATCC, Manassas, VA) and maintained in RPMI 1640 (Roswell Park Memorial Institute) supplemented with 10% FBS and 1% penicillin/streptomycin at 37 C, 5% CO 2 .

    Techniques: Activity Assay, Incubation, MTT Assay, Negative Control, Positive Control

    Viability assay and type of cell death after treatment with the scorpine-like peptide. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazScplp1 (50 μg/mL) or controls (NC: culture medium; PC: 30% DMSO) for 24 h. From left to right, cell viability was assessed using the MTT assay. Representative flow cytometry dot plots (NC vs. BamazScplp1-treated cells) and quantification of apoptotic and necrotic cell death after treatment. Data represent the mean ± SD of triplicate measurements from 1 experiment. NC - negative control (only culture medium). Statistical significance: group vs. NC, * p < 0.05.

    Journal: Frontiers in Pharmacology

    Article Title: A novel scorpine-like peptide from the amazonian scorpion Brotheas amazonicus with cytolytic activity

    doi: 10.3389/fphar.2025.1652614

    Figure Lengend Snippet: Viability assay and type of cell death after treatment with the scorpine-like peptide. MCF10A, SKBR3, MCF7, and MDA-MB-231 cell lines (seeded at 1 × 10 5 cells/well) were treated and incubated with BamazScplp1 (50 μg/mL) or controls (NC: culture medium; PC: 30% DMSO) for 24 h. From left to right, cell viability was assessed using the MTT assay. Representative flow cytometry dot plots (NC vs. BamazScplp1-treated cells) and quantification of apoptotic and necrotic cell death after treatment. Data represent the mean ± SD of triplicate measurements from 1 experiment. NC - negative control (only culture medium). Statistical significance: group vs. NC, * p < 0.05.

    Article Snippet: The breast tumor cell lines SKBr3, MCF-7, and MDA-MB-231, as well as the control breast epithelial cell line MCF10A, were obtained from the American Type Culture Collection (ATCC, Manassas, VA) and maintained in RPMI 1640 (Roswell Park Memorial Institute) supplemented with 10% FBS and 1% penicillin/streptomycin at 37 C, 5% CO 2 .

    Techniques: Viability Assay, Incubation, MTT Assay, Flow Cytometry, Negative Control