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human breast carcinoma mcf 7 cells  (ATCC)


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    ATCC human breast carcinoma mcf 7 cells
    Human Breast Carcinoma Mcf 7 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 34296 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+breast+carcinoma+cells/pmc13179769-74-5-16?v=ATCC
    Average 99 stars, based on 34296 article reviews
    human breast carcinoma mcf 7 cells - by Bioz Stars, 2026-07
    99/100 stars

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    A) Schematic diagram of the experimental design for assessing the motility of Raw264.7 cells after metabolic intervention or hypoxia induction in vitro using living cell imaging technology. B) Representative images and migration tracks of Raw264.7 cells under different treatments. C) Average intracellular ATP content ( n = 3), and D) cell migration velocity under different treatment conditions ( n = 5). E) CLSM images of hypoxia levels in 4T1 <t>and</t> <t>MCF‐7</t> cells marked with hypoxia probes. F) CLSM images of HIF‐1α expression in 4T1 and MCF‐7 cells labeled by immunofluorescence staining. G,H) Semi‐quantitative analysis of hypoxia levels and HIF‐1α expression by fluorescence intensity ( n = 3). Data are presented as mean ± SD. Statistical significance was calculated via one‐way ANOVA with Tukey’ post hoc test. (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
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    Image Search Results


    In vitro biocompatibility evaluation of probe 1 after incubation with MCF-10A cells (A) and MCF-7 (B) cells.

    Journal: RSC Advances

    Article Title: A new indoloquinoline-based fluorescence probe for imaging of hydrazine in vitro and in vivo

    doi: 10.1039/d5ra08919k

    Figure Lengend Snippet: In vitro biocompatibility evaluation of probe 1 after incubation with MCF-10A cells (A) and MCF-7 (B) cells.

    Article Snippet: The human breast carcinoma cells MCF-7 (ATCC, USA), and normal breast epithelial cells MCF-10A (CCTCC, China), were cultured under controlled conditions.

    Techniques: In Vitro, Incubation

    Fluorescence imaging of probe 1 in MCF-7 tumor-bearing mice at various intervals pre- and post-injection.

    Journal: RSC Advances

    Article Title: A new indoloquinoline-based fluorescence probe for imaging of hydrazine in vitro and in vivo

    doi: 10.1039/d5ra08919k

    Figure Lengend Snippet: Fluorescence imaging of probe 1 in MCF-7 tumor-bearing mice at various intervals pre- and post-injection.

    Article Snippet: The human breast carcinoma cells MCF-7 (ATCC, USA), and normal breast epithelial cells MCF-10A (CCTCC, China), were cultured under controlled conditions.

    Techniques: Fluorescence, Imaging, Injection

    Dose–response curves (A,C) and median-effect plots (B,D) generated by CompuSyn software to estimate the IC 50 values of the carotenoid extract against HCT-116 and MDA-MB-231 cell lines.

    Journal: Frontiers in Microbiology

    Article Title: Circular bioeconomy-driven carotenoid production by Agrococcus sp. NP24 using cheese whey byproduct: process optimization and bioactivity assessment

    doi: 10.3389/fmicb.2025.1747717

    Figure Lengend Snippet: Dose–response curves (A,C) and median-effect plots (B,D) generated by CompuSyn software to estimate the IC 50 values of the carotenoid extract against HCT-116 and MDA-MB-231 cell lines.

    Article Snippet: Colorectal carcinoma HCT-116 cell line (RRID: CVCL_0291, ATCC ® CCL-247TM), human hepatoblastoma HepG-2 cell line (RRID: CVCL_0027, ATCC ® Cat. No. HB-8065TM), and human triple negative breast carcinoma (TNBC) MDA-MB-231 cell line (RRID: CVCL0062, ATCC HTB-26TM).

    Techniques: Generated, Software

    A) Schematic diagram of the experimental design for assessing the motility of Raw264.7 cells after metabolic intervention or hypoxia induction in vitro using living cell imaging technology. B) Representative images and migration tracks of Raw264.7 cells under different treatments. C) Average intracellular ATP content ( n = 3), and D) cell migration velocity under different treatment conditions ( n = 5). E) CLSM images of hypoxia levels in 4T1 and MCF‐7 cells marked with hypoxia probes. F) CLSM images of HIF‐1α expression in 4T1 and MCF‐7 cells labeled by immunofluorescence staining. G,H) Semi‐quantitative analysis of hypoxia levels and HIF‐1α expression by fluorescence intensity ( n = 3). Data are presented as mean ± SD. Statistical significance was calculated via one‐way ANOVA with Tukey’ post hoc test. (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Journal: Advanced Science

    Article Title: Photo‐Empowered Macrophage‐Based Drug Delivery System Overcomes Motility Suppression and Significantly Enhances Deep Tumor Drug Delivery

    doi: 10.1002/advs.202515349

    Figure Lengend Snippet: A) Schematic diagram of the experimental design for assessing the motility of Raw264.7 cells after metabolic intervention or hypoxia induction in vitro using living cell imaging technology. B) Representative images and migration tracks of Raw264.7 cells under different treatments. C) Average intracellular ATP content ( n = 3), and D) cell migration velocity under different treatment conditions ( n = 5). E) CLSM images of hypoxia levels in 4T1 and MCF‐7 cells marked with hypoxia probes. F) CLSM images of HIF‐1α expression in 4T1 and MCF‐7 cells labeled by immunofluorescence staining. G,H) Semi‐quantitative analysis of hypoxia levels and HIF‐1α expression by fluorescence intensity ( n = 3). Data are presented as mean ± SD. Statistical significance was calculated via one‐way ANOVA with Tukey’ post hoc test. (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Article Snippet: Mouse breast carcinoma cells 4T1 (RRID: CVCL_0125), human breast carcinoma cells MCF‐7 (RRID: CVCL_0031), and mouse monocyte‐macrophage cells RAW264.7 (RRID: CVCL_0493) were purchased from Procell Life Science & Technology Co., Ltd. (Wuhan, China) in February 2023.

    Techniques: In Vitro, Imaging, Migration, Expressing, Labeling, Immunofluorescence, Staining, Fluorescence