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early passage normal human female colon fibroblast ccd 18co cell line  (ATCC)


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    ATCC early passage normal human female colon fibroblast ccd 18co cell line
    Early Passage Normal Human Female Colon Fibroblast Ccd 18co Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 976 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/colon+ccd+18co+cells/pm42140904-59-1-13?v=ATCC
    Average 97 stars, based on 976 article reviews
    early passage normal human female colon fibroblast ccd 18co cell line - by Bioz Stars, 2026-07
    97/100 stars

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    Histopathology and immunohistochemistry (IHC) analyses. a Representative H&E-stained section from the control group showing normal intestinal architecture with preserved crypt structures (arrows). b H&E-stained section from the CDX group displaying disrupted tissue architecture, densely packed malignant <t>epithelial</t> cells, and invasive tumor margins (arrow). c Immunohistochemical staining for Bax in tumor tissues from the CDX + SFV group, demonstrating increased pro-apoptotic protein expression (arrows). d Immunohistochemical staining for BcL-2 in tumor tissues from the CDX group, indicating strong anti-apoptotic protein expression (arrows). Scale bars: 100 µm ( a , b ), 10 µm ( c , d )
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    Histopathology and immunohistochemistry (IHC) analyses. a Representative H&E-stained section from the control group showing normal intestinal architecture with preserved crypt structures (arrows). b H&E-stained section from the CDX group displaying disrupted tissue architecture, densely packed malignant <t>epithelial</t> cells, and invasive tumor margins (arrow). c Immunohistochemical staining for Bax in tumor tissues from the CDX + SFV group, demonstrating increased pro-apoptotic protein expression (arrows). d Immunohistochemical staining for BcL-2 in tumor tissues from the CDX group, indicating strong anti-apoptotic protein expression (arrows). Scale bars: 100 µm ( a , b ), 10 µm ( c , d )
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    Impact of PDGFRb perturbation within tumor-associated fibroblasts on CRC cell phenotypes. (A) Western blots of t-PDGFRb and p-PDGFRb in <t>CCD-18Co</t> fibroblasts treated with vehicle (Veh), PDGF-BB, or PDGF-BB plus SUN. b-actin serves as a loading control. (B) Quantification of the p-PDGFRb/t-PDGFRb ratio relative to the Veh group. (C) Representative EdU staining of HCT116 cells cultured with CM from the three <t>fibroblast</t> conditions (Veh-CM, PDGF-BB-CM, SUN-CM). EdU (green), DAPI (blue), merged images as indicated. (D) Relative EdU labeling index in HCT116 cells. (E, F) CCK-8 assays showing relative cell viability of HCT116 (E) and DLD-1 (F) cells after 48 h exposure to Veh-CM, PDGF-BB-CM, or SUN-CM. (G) Representative Transwell images of migrated HCT116 and DLD-1 cells under the indicated CM conditions. (H, I) Quantification of migrated HCT116 (H) and DLD-1 (I) cells per 10× field. (J) Violin plots showing concentrations of CCL5, CXCL12, IL-6, IL-10, and TGF-b1 in fibroblast CM measured by ELISA. *P < 0.05, **P < 0.01, ***P < 0.001 vs Veh group; ns, no significant difference. Abbreviations: Veh, vehicle; SUN, sunitinib; CM, conditioned medium; PDGF-BB, the BB homodimer of platelet-derived growth factor.
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    ATCC ccd 18co human colon fibroblast cells
    Cell counts of HCT-116 <t>and</t> <t>CCD-18Co</t> cell lines following treatment with 2.5 μL of magnesium. Non-treated cells group was used as a control group. The treatment led to a decrease in the number of HCT-116 cells, whereas an increase was observed in CCD-18Co cells.
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    Histopathology and immunohistochemistry (IHC) analyses. a Representative H&E-stained section from the control group showing normal intestinal architecture with preserved crypt structures (arrows). b H&E-stained section from the CDX group displaying disrupted tissue architecture, densely packed malignant epithelial cells, and invasive tumor margins (arrow). c Immunohistochemical staining for Bax in tumor tissues from the CDX + SFV group, demonstrating increased pro-apoptotic protein expression (arrows). d Immunohistochemical staining for BcL-2 in tumor tissues from the CDX group, indicating strong anti-apoptotic protein expression (arrows). Scale bars: 100 µm ( a , b ), 10 µm ( c , d )

    Journal: Investigational New Drugs

    Article Title: Scorpio fuscus venom as a promising anticancer agent against colorectal cancer

    doi: 10.1007/s10637-026-01598-z

    Figure Lengend Snippet: Histopathology and immunohistochemistry (IHC) analyses. a Representative H&E-stained section from the control group showing normal intestinal architecture with preserved crypt structures (arrows). b H&E-stained section from the CDX group displaying disrupted tissue architecture, densely packed malignant epithelial cells, and invasive tumor margins (arrow). c Immunohistochemical staining for Bax in tumor tissues from the CDX + SFV group, demonstrating increased pro-apoptotic protein expression (arrows). d Immunohistochemical staining for BcL-2 in tumor tissues from the CDX group, indicating strong anti-apoptotic protein expression (arrows). Scale bars: 100 µm ( a , b ), 10 µm ( c , d )

    Article Snippet: Human CRC cell lines (DLD-1, HT-29, Caco-2) and human healthy colon epithelial cell line (CCD-18Co) were purchased from the American Type Culture Collection (ATCC, Rockville, MD).

    Techniques: Histopathology, Immunohistochemistry, Staining, Control, Immunohistochemical staining, Expressing

    Impact of PDGFRb perturbation within tumor-associated fibroblasts on CRC cell phenotypes. (A) Western blots of t-PDGFRb and p-PDGFRb in CCD-18Co fibroblasts treated with vehicle (Veh), PDGF-BB, or PDGF-BB plus SUN. b-actin serves as a loading control. (B) Quantification of the p-PDGFRb/t-PDGFRb ratio relative to the Veh group. (C) Representative EdU staining of HCT116 cells cultured with CM from the three fibroblast conditions (Veh-CM, PDGF-BB-CM, SUN-CM). EdU (green), DAPI (blue), merged images as indicated. (D) Relative EdU labeling index in HCT116 cells. (E, F) CCK-8 assays showing relative cell viability of HCT116 (E) and DLD-1 (F) cells after 48 h exposure to Veh-CM, PDGF-BB-CM, or SUN-CM. (G) Representative Transwell images of migrated HCT116 and DLD-1 cells under the indicated CM conditions. (H, I) Quantification of migrated HCT116 (H) and DLD-1 (I) cells per 10× field. (J) Violin plots showing concentrations of CCL5, CXCL12, IL-6, IL-10, and TGF-b1 in fibroblast CM measured by ELISA. *P < 0.05, **P < 0.01, ***P < 0.001 vs Veh group; ns, no significant difference. Abbreviations: Veh, vehicle; SUN, sunitinib; CM, conditioned medium; PDGF-BB, the BB homodimer of platelet-derived growth factor.

    Journal: Frontiers in Immunology

    Article Title: From multi-omics to functional validation: the PTMRS stratifies TME and positions PDGFRB in CRC biology

    doi: 10.3389/fimmu.2025.1728291

    Figure Lengend Snippet: Impact of PDGFRb perturbation within tumor-associated fibroblasts on CRC cell phenotypes. (A) Western blots of t-PDGFRb and p-PDGFRb in CCD-18Co fibroblasts treated with vehicle (Veh), PDGF-BB, or PDGF-BB plus SUN. b-actin serves as a loading control. (B) Quantification of the p-PDGFRb/t-PDGFRb ratio relative to the Veh group. (C) Representative EdU staining of HCT116 cells cultured with CM from the three fibroblast conditions (Veh-CM, PDGF-BB-CM, SUN-CM). EdU (green), DAPI (blue), merged images as indicated. (D) Relative EdU labeling index in HCT116 cells. (E, F) CCK-8 assays showing relative cell viability of HCT116 (E) and DLD-1 (F) cells after 48 h exposure to Veh-CM, PDGF-BB-CM, or SUN-CM. (G) Representative Transwell images of migrated HCT116 and DLD-1 cells under the indicated CM conditions. (H, I) Quantification of migrated HCT116 (H) and DLD-1 (I) cells per 10× field. (J) Violin plots showing concentrations of CCL5, CXCL12, IL-6, IL-10, and TGF-b1 in fibroblast CM measured by ELISA. *P < 0.05, **P < 0.01, ***P < 0.001 vs Veh group; ns, no significant difference. Abbreviations: Veh, vehicle; SUN, sunitinib; CM, conditioned medium; PDGF-BB, the BB homodimer of platelet-derived growth factor.

    Article Snippet: Human CRC cell line HCT116 and colonic fibroblast cell line (CCD-18Co) were obtained from the American Type Culture Collection (ATCC) and cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin at 37 °C in a 5% CO 2 humidified incubator.

    Techniques: Western Blot, Control, Staining, Cell Culture, Labeling, CCK-8 Assay, Enzyme-linked Immunosorbent Assay, Derivative Assay

    Cell counts of HCT-116 and CCD-18Co cell lines following treatment with 2.5 μL of magnesium. Non-treated cells group was used as a control group. The treatment led to a decrease in the number of HCT-116 cells, whereas an increase was observed in CCD-18Co cells.

    Journal: Scientific Reports

    Article Title: Investigating the potential selective effects of a Kiperin multi-component magnesium supplement on colon cancer and normal cells

    doi: 10.1038/s41598-025-32854-6

    Figure Lengend Snippet: Cell counts of HCT-116 and CCD-18Co cell lines following treatment with 2.5 μL of magnesium. Non-treated cells group was used as a control group. The treatment led to a decrease in the number of HCT-116 cells, whereas an increase was observed in CCD-18Co cells.

    Article Snippet: Two cell lines were used: CCD-18Co human colon fibroblast cells (CRL-1459) and HCT-116 human colon cancer cells (CCL-247), both obtained from the American Type Culture Collection (ATCC).

    Techniques: Control

    Scratch wound assay for evaluating the cell migration of CCD-18Co and HCT116 cell lines at 0, 6, 18 and 24 h after 2.5 μL of magnesium treatment. Non-treated cells group was used as a control group.

    Journal: Scientific Reports

    Article Title: Investigating the potential selective effects of a Kiperin multi-component magnesium supplement on colon cancer and normal cells

    doi: 10.1038/s41598-025-32854-6

    Figure Lengend Snippet: Scratch wound assay for evaluating the cell migration of CCD-18Co and HCT116 cell lines at 0, 6, 18 and 24 h after 2.5 μL of magnesium treatment. Non-treated cells group was used as a control group.

    Article Snippet: Two cell lines were used: CCD-18Co human colon fibroblast cells (CRL-1459) and HCT-116 human colon cancer cells (CCL-247), both obtained from the American Type Culture Collection (ATCC).

    Techniques: Scratch Wound Assay Assay, Migration, Control

    Gene expression in CCD-18Co cells with and without 2.5 μL magnesium supplement. VDR and TNFα gene expression levels were significantly altered. Non-treated cells group was used as a control group.

    Journal: Scientific Reports

    Article Title: Investigating the potential selective effects of a Kiperin multi-component magnesium supplement on colon cancer and normal cells

    doi: 10.1038/s41598-025-32854-6

    Figure Lengend Snippet: Gene expression in CCD-18Co cells with and without 2.5 μL magnesium supplement. VDR and TNFα gene expression levels were significantly altered. Non-treated cells group was used as a control group.

    Article Snippet: Two cell lines were used: CCD-18Co human colon fibroblast cells (CRL-1459) and HCT-116 human colon cancer cells (CCL-247), both obtained from the American Type Culture Collection (ATCC).

    Techniques: Gene Expression, Control