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human colon epithelial cell line caco  (ATCC)


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    ATCC human colon epithelial cell line caco
    Human Colon Epithelial Cell Line Caco, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 15122 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+colon+epithelial+caco+2+cells/Caco-2/pm41653758-129-1-29
    Average 99 stars, based on 15122 article reviews
    human colon epithelial cell line caco - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    In Vitro:

    Article Title: Influences of a standardized food matrix and gastrointestinal fluids on the physicochemical properties of titanium dioxide nanoparticles
    Article Snippet: .. Then, a nanotoxicology case study was carried out to assess the toxicity of the digested e-TiO2-NPs using an in vitro cellularmodel of human colon epithelial Caco-2 cells (ATCC; SCSP5027). ..

    Article Title: Influences of a standardized food matrix and gastrointestinal fluids on the physicochemical properties of titanium dioxide nanoparticles
    Article Snippet: .. Then, a nanotoxicology case study was carried out to assess the toxicity of the digested e-TiO 2 -NPs using an in vitro cellular model of human colon epithelial Caco-2 cells (ATCC; SCSP-5027). ..

    Modification:

    Article Title: Influences of a standardized food matrix and gastrointestinal fluids on the physicochemical properties of titanium dioxide nanoparticles
    Article Snippet: The solubility of the e-TiO 2 -NPs suspensions was measured using an ICP-AES730 (Agilent Technologies, Santa Clara, CA, USA); the supernatants were collected by ultracentrifugation (10 000 × g ) for 1 h as described for the ICP-AES analysis. .. Human colon epithelial Caco-2 cells (ATCC; SCSP-5027) were grown in Dulbecco's modified Eagle's medium/high glucose medium (Hyclone, Shanghai, China) supplemented with 10% heat-inactivated fetal bovine serum (Gibco, Shanghai, China), 1% penicillin–streptomycin solution (Hyclone, Shanghai, China) and non-essential amino acids (1/100 dilution of 100× solution, Gibco, Shanghai, China). ..

    Cell Culture:

    Article Title: Methylated tirilazad alleviates DSS-induced colitis in mice through reciprocal microbiome-metabolome.
    Article Snippet: .. Human colon epithelial Caco-2 cells (ATCC HTB-37) were cultured in complete medium containing 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin at 37 ◦C in a 5% CO2 incubator. ..



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    Measurement of pro-inflammatory cytokine secretion levels in the co-culture system. Analyses were conducted evaluating ( A ) IL-8 levels in the apical medium <t>(differentiated</t> <t>Caco-2</t> cells) and ( B ) IL-6 and ( C ) TNF-α levels in the basolateral medium (RAW264.7 cells). Caco-2 cells were pre-treated for 90 min with BD, BFM (1/20, v / v ), and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. Data are expressed as mean ± SD of three experiments conducted in triplicate. Different letters (a–e) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).
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    ATCC human colonic epithelial caco 2 cells
    Shown are 3D renderings of confocal images <t>of</t> <t>Caco-2</t> cells stained with 300 nM of DAPI (blue) for nuclei, 3 μg/mL of FM 4-64 (red) for membranes, and 1.5 µM FITC-labeled peptides (green). The total size of each image is 220 × 220 × 28 µm.
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    ATCC staining human colonic epithelial caco 2 cells
    Shown are 3D renderings of confocal images <t>of</t> <t>Caco-2</t> cells stained with 300 nM of DAPI (blue) for nuclei, 3 μg/mL of FM 4-64 (red) for membranes, and 1.5 µM FITC-labeled peptides (green). The total size of each image is 220 × 220 × 28 µm.
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    Image Search Results


    Measurement of pro-inflammatory cytokine secretion levels in the co-culture system. Analyses were conducted evaluating ( A ) IL-8 levels in the apical medium (differentiated Caco-2 cells) and ( B ) IL-6 and ( C ) TNF-α levels in the basolateral medium (RAW264.7 cells). Caco-2 cells were pre-treated for 90 min with BD, BFM (1/20, v / v ), and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. Data are expressed as mean ± SD of three experiments conducted in triplicate. Different letters (a–e) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Measurement of pro-inflammatory cytokine secretion levels in the co-culture system. Analyses were conducted evaluating ( A ) IL-8 levels in the apical medium (differentiated Caco-2 cells) and ( B ) IL-6 and ( C ) TNF-α levels in the basolateral medium (RAW264.7 cells). Caco-2 cells were pre-treated for 90 min with BD, BFM (1/20, v / v ), and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. Data are expressed as mean ± SD of three experiments conducted in triplicate. Different letters (a–e) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Co-Culture Assay, Positive Control, Concentration Assay

    Evaluation of iNOS protein levels in differentiated Caco-2 cells and NOx release into the apical medium. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative immunoblot (IB) images and ( B ) densitometric analysis of iNOS levels normalized to β-Actin. ( C ) NOx concentration. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Evaluation of iNOS protein levels in differentiated Caco-2 cells and NOx release into the apical medium. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative immunoblot (IB) images and ( B ) densitometric analysis of iNOS levels normalized to β-Actin. ( C ) NOx concentration. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Positive Control, Concentration Assay, Western Blot

    Measurement of intracellular ROS production in differentiated Caco-2 cells. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative fluorescence histograms and ( B ) quantitative analysis of ROS generation. Data are expressed as mean ± SD of three experiments conducted in triplicate. Different letters (a–e) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Measurement of intracellular ROS production in differentiated Caco-2 cells. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative fluorescence histograms and ( B ) quantitative analysis of ROS generation. Data are expressed as mean ± SD of three experiments conducted in triplicate. Different letters (a–e) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Positive Control, Concentration Assay, Fluorescence

    Assessment of occludin protein levels in differentiated Caco-2 cells. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative immunoblot (IB) images and ( B ) densitometric analysis of occludin levels normalized to β-Actin. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Assessment of occludin protein levels in differentiated Caco-2 cells. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative immunoblot (IB) images and ( B ) densitometric analysis of occludin levels normalized to β-Actin. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Positive Control, Concentration Assay, Western Blot

    Evaluation of NF-κB p65 nuclear translocation levels in RAW264.7 cells. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative immunoblot (IB) images and ( B , C ) densitometric analysis of NF-κB p65 levels in cytosolic and nuclear fractions, normalized to β-Actin and Lamin B1, respectively. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Evaluation of NF-κB p65 nuclear translocation levels in RAW264.7 cells. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representative immunoblot (IB) images and ( B , C ) densitometric analysis of NF-κB p65 levels in cytosolic and nuclear fractions, normalized to β-Actin and Lamin B1, respectively. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Translocation Assay, Positive Control, Concentration Assay, Western Blot

    Assessment of COX-2 protein levels in RAW264.7 cells and PGE 2 secretion into the basolateral medium. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representatives immunoblot (IB) images and ( B ) densitometric analysis of COX-2 levels normalized to β-Actin. ( C ) PGE 2 concentration. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Assessment of COX-2 protein levels in RAW264.7 cells and PGE 2 secretion into the basolateral medium. Caco-2 cells were pre-treated for 90 min with BFM (1/20, v / v ) and budesonide (1 µM, positive control), as indicated by (+), while absence of treatment is indicated by (−). Subsequently, RAW264.7 macrophages were stimulated with LPS at a concentration of 1 µg/mL for 24 h. ( A ) Representatives immunoblot (IB) images and ( B ) densitometric analysis of COX-2 levels normalized to β-Actin. ( C ) PGE 2 concentration. Data are expressed as mean ± SD ( n = 3). Different letters (a–d) indicate statistically significant differences among all groups within each panel ( p < 0.05) (one-way ANOVA followed by Tukey’s test).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Positive Control, Concentration Assay, Western Blot

    Evaluation of pharmacological interactions between budesonide and BFM using CI analysis on different inflammatory markers. Measurements were performed in the apical medium (differentiated Caco-2 cells: IL-8, NOx; RAW264.7 macrophages: IL-6, TNF-α, PGE 2 ) and intracellularly (differentiated Caco-2 cells: iNOS, ROS, occludin; RAW264.7 macrophages: NF-κB p65, COX-2). A CI ratio less than 1 indicates antagonism (–), equal to 1 represents additivity (+), and greater than 1 demonstrates synergy (++). Data are expressed as mean ± SD ( n = 3).

    Journal: Antioxidants

    Article Title: Anti-Inflammatory Activity of In Vitro Digested Manna in a Caco-2 and RAW264.7 Cells Co-Culture Model of Inflammatory Bowel Disease

    doi: 10.3390/antiox15050601

    Figure Lengend Snippet: Evaluation of pharmacological interactions between budesonide and BFM using CI analysis on different inflammatory markers. Measurements were performed in the apical medium (differentiated Caco-2 cells: IL-8, NOx; RAW264.7 macrophages: IL-6, TNF-α, PGE 2 ) and intracellularly (differentiated Caco-2 cells: iNOS, ROS, occludin; RAW264.7 macrophages: NF-κB p65, COX-2). A CI ratio less than 1 indicates antagonism (–), equal to 1 represents additivity (+), and greater than 1 demonstrates synergy (++). Data are expressed as mean ± SD ( n = 3).

    Article Snippet: Human colonic epithelial adenocarcinoma (Caco-2) cells and murine macrophage/monocyte (RAW264.7) cell lines were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques:

    Shown are 3D renderings of confocal images of Caco-2 cells stained with 300 nM of DAPI (blue) for nuclei, 3 μg/mL of FM 4-64 (red) for membranes, and 1.5 µM FITC-labeled peptides (green). The total size of each image is 220 × 220 × 28 µm.

    Journal: PLOS Pathogens

    Article Title: Conformations and sequence determinants in the lipid binding of an adhesive peptide derived from Vibrio cholerae biofilms

    doi: 10.1371/journal.ppat.1013990

    Figure Lengend Snippet: Shown are 3D renderings of confocal images of Caco-2 cells stained with 300 nM of DAPI (blue) for nuclei, 3 μg/mL of FM 4-64 (red) for membranes, and 1.5 µM FITC-labeled peptides (green). The total size of each image is 220 × 220 × 28 µm.

    Article Snippet: Human colonic epithelial Caco-2 cells (ATCC HTB-37) were obtained from ATCC and authenticated by ATCC based on morphology, doubling time, and STR profiling.

    Techniques: Staining, Labeling