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mouse fibroblast cell lines  (ATCC)


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    Structured Review

    ATCC mouse fibroblast cell lines
    Mouse Fibroblast Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 956 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mice+fibroblast+colon+carcinoma+cells/HCT+116%3B+Colon+Carcinoma%3B+Human/pmc12962158-273-27-32
    Average 97 stars, based on 956 article reviews
    mouse fibroblast cell lines - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    Fluorescence:

    Article Title: Dynamic Excimer (DYNEX) Imaging of Lipid Droplets.
    Article Snippet: .. S5 Cell cultures for fluorescence imaging Human fibroblast normal colon (CCD-18Co; ATCC CRL-1459) and mice fibroblast colon carcinoma cells (CT26.WT; ATCC CRL-2638) were provided by the Cell Culture Facility of the University of Granada. ..

    Imaging:

    Article Title: Dynamic Excimer (DYNEX) Imaging of Lipid Droplets.
    Article Snippet: .. S5 Cell cultures for fluorescence imaging Human fibroblast normal colon (CCD-18Co; ATCC CRL-1459) and mice fibroblast colon carcinoma cells (CT26.WT; ATCC CRL-2638) were provided by the Cell Culture Facility of the University of Granada. ..

    Cell Culture:

    Article Title: Dynamic Excimer (DYNEX) Imaging of Lipid Droplets.
    Article Snippet: .. S5 Cell cultures for fluorescence imaging Human fibroblast normal colon (CCD-18Co; ATCC CRL-1459) and mice fibroblast colon carcinoma cells (CT26.WT; ATCC CRL-2638) were provided by the Cell Culture Facility of the University of Granada. ..



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    ATCC healthy mouse fibroblast cell line l929
    Determination of the IC 50 values of 4-AP in <t>L929</t> and MCF-7 cell lines. Concentrations of 25 mM, 12.5 mM, and 6.25 mM were used as the highest doses. Since the expected IC 50 range was between 1 and 5 mM, finer dose increments of 1 mM were applied within this range. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Following viability measurements, inhibitor vs. response curves were plotted to calculate IC 50 values. The IC 50 value of 4-AP was determined to be 5 mM in L929 cells ( a ) and 4 mM in MCF-7 cells ( b ). Data represent mean ± SEM from more than three independent experiments ( n ≥ 3).
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    Determination of the IC 50 values of 4-AP in <t>L929</t> and MCF-7 cell lines. Concentrations of 25 mM, 12.5 mM, and 6.25 mM were used as the highest doses. Since the expected IC 50 range was between 1 and 5 mM, finer dose increments of 1 mM were applied within this range. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Following viability measurements, inhibitor vs. response curves were plotted to calculate IC 50 values. The IC 50 value of 4-AP was determined to be 5 mM in L929 cells ( a ) and 4 mM in MCF-7 cells ( b ). Data represent mean ± SEM from more than three independent experiments ( n ≥ 3).
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    Determination of the IC 50 values of 4-AP in L929 and MCF-7 cell lines. Concentrations of 25 mM, 12.5 mM, and 6.25 mM were used as the highest doses. Since the expected IC 50 range was between 1 and 5 mM, finer dose increments of 1 mM were applied within this range. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Following viability measurements, inhibitor vs. response curves were plotted to calculate IC 50 values. The IC 50 value of 4-AP was determined to be 5 mM in L929 cells ( a ) and 4 mM in MCF-7 cells ( b ). Data represent mean ± SEM from more than three independent experiments ( n ≥ 3).

    Journal: International Journal of Molecular Sciences

    Article Title: Targeting Voltage-Gated Potassium Channels in Breast Cancer: Mechanistic Insights into 4-Aminopyridine-Induced Cell Death

    doi: 10.3390/ijms26167768

    Figure Lengend Snippet: Determination of the IC 50 values of 4-AP in L929 and MCF-7 cell lines. Concentrations of 25 mM, 12.5 mM, and 6.25 mM were used as the highest doses. Since the expected IC 50 range was between 1 and 5 mM, finer dose increments of 1 mM were applied within this range. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Following viability measurements, inhibitor vs. response curves were plotted to calculate IC 50 values. The IC 50 value of 4-AP was determined to be 5 mM in L929 cells ( a ) and 4 mM in MCF-7 cells ( b ). Data represent mean ± SEM from more than three independent experiments ( n ≥ 3).

    Article Snippet: The breast cancer cell line MCF-7 (ATCC HTB 22) and healthy mouse fibroblast cell line L929 (ATCC CCL-1) were used in this study.

    Techniques:

    Assessment of cell viability following CHX and 4-AP treatments. Cells were treated with the IC 50 concentration of 4-AP, and cell viability was assessed using the trypan blue exclusion method with a hemocytometer. For CHX treatment, a 20 µM dose was selected. Cells were pre-incubated with CHX for 1 h prior to 4-AP exposure. CHX pre-treatment resulted in increased cell viability in both the L929 ( A ) and MCF-7 ( B ) cell lines. *** p < 0.001, and **** p < 0.0001, n ≥ 3.

    Journal: International Journal of Molecular Sciences

    Article Title: Targeting Voltage-Gated Potassium Channels in Breast Cancer: Mechanistic Insights into 4-Aminopyridine-Induced Cell Death

    doi: 10.3390/ijms26167768

    Figure Lengend Snippet: Assessment of cell viability following CHX and 4-AP treatments. Cells were treated with the IC 50 concentration of 4-AP, and cell viability was assessed using the trypan blue exclusion method with a hemocytometer. For CHX treatment, a 20 µM dose was selected. Cells were pre-incubated with CHX for 1 h prior to 4-AP exposure. CHX pre-treatment resulted in increased cell viability in both the L929 ( A ) and MCF-7 ( B ) cell lines. *** p < 0.001, and **** p < 0.0001, n ≥ 3.

    Article Snippet: The breast cancer cell line MCF-7 (ATCC HTB 22) and healthy mouse fibroblast cell line L929 (ATCC CCL-1) were used in this study.

    Techniques: Concentration Assay, Incubation

    Assessment of cell viability following Z-VAD-FMK and 4-AP treatments. Cells were treated with 50 µM Z-VAD-FMK, either alone or in combination with 4-AP. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Treatment with Z-VAD-FMK alone resulted in a slight decrease in cell viability compared to the control group. However, pre-treatment with Z-VAD-FMK for 1 h prior to 4-AP exposure significantly reduced cell viability in both L929 ( A ) and MCF-7 ( B ) cell lines. ** p < 0.01, **** p < 0.0001, n ≥ 3.

    Journal: International Journal of Molecular Sciences

    Article Title: Targeting Voltage-Gated Potassium Channels in Breast Cancer: Mechanistic Insights into 4-Aminopyridine-Induced Cell Death

    doi: 10.3390/ijms26167768

    Figure Lengend Snippet: Assessment of cell viability following Z-VAD-FMK and 4-AP treatments. Cells were treated with 50 µM Z-VAD-FMK, either alone or in combination with 4-AP. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Treatment with Z-VAD-FMK alone resulted in a slight decrease in cell viability compared to the control group. However, pre-treatment with Z-VAD-FMK for 1 h prior to 4-AP exposure significantly reduced cell viability in both L929 ( A ) and MCF-7 ( B ) cell lines. ** p < 0.01, **** p < 0.0001, n ≥ 3.

    Article Snippet: The breast cancer cell line MCF-7 (ATCC HTB 22) and healthy mouse fibroblast cell line L929 (ATCC CCL-1) were used in this study.

    Techniques: Control

    Assessment of cell viability following 2-APB and 4-AP treatments. Cells were treated with 10 µM 2-APB, either alone or in combination with 4-AP. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Pre-treatment with 2-APB for 1 h increased cell viability in both L929 ( A ) and MCF-7 ( B ) cell lines. *** p < 0.001, and **** p < 0.0001, n ≥ 3.

    Journal: International Journal of Molecular Sciences

    Article Title: Targeting Voltage-Gated Potassium Channels in Breast Cancer: Mechanistic Insights into 4-Aminopyridine-Induced Cell Death

    doi: 10.3390/ijms26167768

    Figure Lengend Snippet: Assessment of cell viability following 2-APB and 4-AP treatments. Cells were treated with 10 µM 2-APB, either alone or in combination with 4-AP. Cell viability was assessed using the trypan blue exclusion method with a hemocytometer. Pre-treatment with 2-APB for 1 h increased cell viability in both L929 ( A ) and MCF-7 ( B ) cell lines. *** p < 0.001, and **** p < 0.0001, n ≥ 3.

    Article Snippet: The breast cancer cell line MCF-7 (ATCC HTB 22) and healthy mouse fibroblast cell line L929 (ATCC CCL-1) were used in this study.

    Techniques:

    Percentage changes in intracellular Ca 2+ levels following treatments. Intracellular calcium concentrations were measured using the Fura-2 fluorescent dye. Percentage changes in Ca 2+ levels were calculated relative to the untreated control group. Treatment with 4-AP and its combinations increased intracellular Ca 2+ levels. CHX and Z-VAD-FMK alone did not induce significant increases, whereas 2-APB alone elevated intracellular Ca 2+ concentrations in both L929 ( A ) and MCF-7 ( B ) cell lines. * p < 0.05, *** p < 0.001, and **** p < 0.0001, n ≥ 3. Non-significant results are not indicated in the figure.

    Journal: International Journal of Molecular Sciences

    Article Title: Targeting Voltage-Gated Potassium Channels in Breast Cancer: Mechanistic Insights into 4-Aminopyridine-Induced Cell Death

    doi: 10.3390/ijms26167768

    Figure Lengend Snippet: Percentage changes in intracellular Ca 2+ levels following treatments. Intracellular calcium concentrations were measured using the Fura-2 fluorescent dye. Percentage changes in Ca 2+ levels were calculated relative to the untreated control group. Treatment with 4-AP and its combinations increased intracellular Ca 2+ levels. CHX and Z-VAD-FMK alone did not induce significant increases, whereas 2-APB alone elevated intracellular Ca 2+ concentrations in both L929 ( A ) and MCF-7 ( B ) cell lines. * p < 0.05, *** p < 0.001, and **** p < 0.0001, n ≥ 3. Non-significant results are not indicated in the figure.

    Article Snippet: The breast cancer cell line MCF-7 (ATCC HTB 22) and healthy mouse fibroblast cell line L929 (ATCC CCL-1) were used in this study.

    Techniques: Control

    Effect of drug treatments on membrane polarization. To assess the effects of elevated intracellular Ca 2+ levels on membrane potential, DiBAC 4 (3) fluorescent dye was used. Since CHX and Z-VAD-FMK did not induce significant increases in intracellular Ca 2+ levels, they were excluded from DiBAC 4 (3) measurements. Treatment with 4-AP and its combinations increased membrane depolarization, with the most pronounced effect observed following co-treatment with 2-APB. In contrast, 2-APB alone did not cause substantial depolarization in either L929 ( A ) or MCF-7 ( B ) cell lines. **** p < 0.0001, n ≥ 3. Non-significant results are not indicated in the figure.

    Journal: International Journal of Molecular Sciences

    Article Title: Targeting Voltage-Gated Potassium Channels in Breast Cancer: Mechanistic Insights into 4-Aminopyridine-Induced Cell Death

    doi: 10.3390/ijms26167768

    Figure Lengend Snippet: Effect of drug treatments on membrane polarization. To assess the effects of elevated intracellular Ca 2+ levels on membrane potential, DiBAC 4 (3) fluorescent dye was used. Since CHX and Z-VAD-FMK did not induce significant increases in intracellular Ca 2+ levels, they were excluded from DiBAC 4 (3) measurements. Treatment with 4-AP and its combinations increased membrane depolarization, with the most pronounced effect observed following co-treatment with 2-APB. In contrast, 2-APB alone did not cause substantial depolarization in either L929 ( A ) or MCF-7 ( B ) cell lines. **** p < 0.0001, n ≥ 3. Non-significant results are not indicated in the figure.

    Article Snippet: The breast cancer cell line MCF-7 (ATCC HTB 22) and healthy mouse fibroblast cell line L929 (ATCC CCL-1) were used in this study.

    Techniques: Membrane