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human normal breast epithelial cell line mcf 10a  (Procell Inc)

 
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    Procell Inc human normal breast epithelial cell line mcf 10a
    Human Normal Breast Epithelial Cell Line Mcf 10a, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+normal+breast+epithelial+cell+line+mcf+10a/cells+h9c2/pm41605797-69-0-28
    Average 86 stars, based on 1 article reviews
    human normal breast epithelial cell line mcf 10a - by Bioz Stars, 2026-10
    86/100 stars

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    Multiple Displacement Amplification:

    Article Title: Astragalus Polysaccharide Attenuates Breast Cancer Progression by Regulating METTL3-Mediated MAL2 m 6 A Modification
    Article Snippet: .. Human normal breast epithelial cell line MCF-10A (cat. no. CL-0525), and two BC cell lines including MCF-7 (cat. no. CL-0149) and MDA-MB-231 (cat. no. CL-0150) were purchased from Procell, China. .. The MCF-10A cells were cultured in CM-0525 medium (Procell), and the BC cell lines were cultured in DMEM medium (Procell) containing 10% FBS (Procell) and were incubated under the condition of 5% CO 2 and 37°C.

    Article Title: Astragalus Polysaccharide Attenuates Breast Cancer Progression by Regulating METTL3-Mediated MAL2 m 6 A Modification.
    Article Snippet: Introduction Breast cancer (BC) is the most widespread malignancy that affects females globally, with more than 2.3 million cases and nearly 665,000 deaths reported alone in the year 2022 [1].. BC is a complex disease driven by both genetic and environmental factors, with current treatment options including surgery, chemoradiotherapy, endocrine therapy, and targeted therapy widely used in clinical practice [2].. Nonetheless, while various chemo preventive drugs are effectively used to treat BC, challenges such as chemoresistance and metastasis persist in certain patients, particularly in triple-negative BC, often resulting in a poor prognosis [3].



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    human normal breast epithelial cell line mcf 10a  (Procell Inc)
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    Figure 6. STAT3 phosphorylation had an inverse effect on CREB3L1 protein expression in TNBC. (a) Western blot analysis comparing the expression of STAT3, pSTAT3, and CREB3L1 in TNBC cells treated with scRNA to the same cell lines with ROR1 expression knocked down (siROR1). (b) Quantification of Western blot analysis (n = 3). Statistical significance was determined through paired Student’s t-test (* p < 0.05, ** p < 0.01). (c) Western blot analysis comparing the protein expression of ROR1, STAT3, pSTAT3, DNMT3A, DNMT3B, and CREB3L1 in naive <t>MCF10A</t> cells compared to the same cell line that has been transfected with IL-6 recombinant protein (* p < 0.05, ** p < 0.01, n = 3).
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    Fig. 1 AIM2 expression is decreased in breast cancer tissues and cells. (A) RT-qPCR analysis and (B) Western blot analysis of AIM2 expression in breast cancer tissues and adjacent non-cancerous tissues (representative results from a total of 60 cases). β-actin served as a loading control. (C) RT-qPCR analysis and (D) Western blot analysis of AIM2 expression in normal breast epithelial cells <t>(MCF10A)</t> and breast cancer cell lines (MCF7, T47D, BT474, MDA-MB-231, BT549). Statistical significance was determined using one-way ANOVA followed by Tukey’s post-hoc test for multiple comparisons. *P < 0.05, **P < 0.01
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    Fig. 1 AIM2 expression is decreased in breast cancer tissues and cells. (A) RT-qPCR analysis and (B) Western blot analysis of AIM2 expression in breast cancer tissues and adjacent non-cancerous tissues (representative results from a total of 60 cases). β-actin served as a loading control. (C) RT-qPCR analysis and (D) Western blot analysis of AIM2 expression in normal breast epithelial cells <t>(MCF10A)</t> and breast cancer cell lines (MCF7, T47D, BT474, MDA-MB-231, BT549). Statistical significance was determined using one-way ANOVA followed by Tukey’s post-hoc test for multiple comparisons. *P < 0.05, **P < 0.01
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    Figure 6. STAT3 phosphorylation had an inverse effect on CREB3L1 protein expression in TNBC. (a) Western blot analysis comparing the expression of STAT3, pSTAT3, and CREB3L1 in TNBC cells treated with scRNA to the same cell lines with ROR1 expression knocked down (siROR1). (b) Quantification of Western blot analysis (n = 3). Statistical significance was determined through paired Student’s t-test (* p < 0.05, ** p < 0.01). (c) Western blot analysis comparing the protein expression of ROR1, STAT3, pSTAT3, DNMT3A, DNMT3B, and CREB3L1 in naive MCF10A cells compared to the same cell line that has been transfected with IL-6 recombinant protein (* p < 0.05, ** p < 0.01, n = 3).

    Journal: Biomolecules

    Article Title: Uncovering a Novel Role of ROR1 in the Epigenetic Regulation of Tumor Suppressor Gene CREB3L1 in Triple-Negative Breast Cancer Cells.

    doi: 10.3390/biom15050734

    Figure Lengend Snippet: Figure 6. STAT3 phosphorylation had an inverse effect on CREB3L1 protein expression in TNBC. (a) Western blot analysis comparing the expression of STAT3, pSTAT3, and CREB3L1 in TNBC cells treated with scRNA to the same cell lines with ROR1 expression knocked down (siROR1). (b) Quantification of Western blot analysis (n = 3). Statistical significance was determined through paired Student’s t-test (* p < 0.05, ** p < 0.01). (c) Western blot analysis comparing the protein expression of ROR1, STAT3, pSTAT3, DNMT3A, DNMT3B, and CREB3L1 in naive MCF10A cells compared to the same cell line that has been transfected with IL-6 recombinant protein (* p < 0.05, ** p < 0.01, n = 3).

    Article Snippet: Cell Culture TNBC cell lines MDA-MB-231 (HTB 26, ATCC, Manassas, VA, USA), HCC1806 (CRL2335, ATCC, Manassas, VA, USA), and normal human epithelial breast cell line MCF10A (CRL-10317, ATCC, Manassas, VA, USA) are cultured as recommended by ATCC.

    Techniques: Phospho-proteomics, Expressing, Western Blot, Transfection, Recombinant

    Fig. 1 AIM2 expression is decreased in breast cancer tissues and cells. (A) RT-qPCR analysis and (B) Western blot analysis of AIM2 expression in breast cancer tissues and adjacent non-cancerous tissues (representative results from a total of 60 cases). β-actin served as a loading control. (C) RT-qPCR analysis and (D) Western blot analysis of AIM2 expression in normal breast epithelial cells (MCF10A) and breast cancer cell lines (MCF7, T47D, BT474, MDA-MB-231, BT549). Statistical significance was determined using one-way ANOVA followed by Tukey’s post-hoc test for multiple comparisons. *P < 0.05, **P < 0.01

    Journal: Epigenetics & chromatin

    Article Title: Acetylation modification of AIM2 by KAT2B suppresses the AKT/Wnt/β-catenin signaling pathway activation and inhibits breast cancer progression.

    doi: 10.1186/s13072-025-00591-9

    Figure Lengend Snippet: Fig. 1 AIM2 expression is decreased in breast cancer tissues and cells. (A) RT-qPCR analysis and (B) Western blot analysis of AIM2 expression in breast cancer tissues and adjacent non-cancerous tissues (representative results from a total of 60 cases). β-actin served as a loading control. (C) RT-qPCR analysis and (D) Western blot analysis of AIM2 expression in normal breast epithelial cells (MCF10A) and breast cancer cell lines (MCF7, T47D, BT474, MDA-MB-231, BT549). Statistical significance was determined using one-way ANOVA followed by Tukey’s post-hoc test for multiple comparisons. *P < 0.05, **P < 0.01

    Article Snippet: Human normal breast epithelial cell line MCF10A and breast cancer cell lines (MCF7, T47D, BT474, MDAMB-231, and BT549) were obtained from ATCC and grown in grown in Ham’s F12 medium/DMEM (Gibco, Grand Island, NY, USA) with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin.

    Techniques: Expressing, Quantitative RT-PCR, Western Blot, Control