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    CLS Cell Lines Service GmbH g 0 50 100 150 200 250 300 350
    G 0 50 100 150 200 250 300 350, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 90/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sw-403+cells/SW-403+Cells/10__1007_slash_jhep05_ascii40_2019_ascii41_142-760-27-65
    Average 90 stars, based on 8 article reviews
    g 0 50 100 150 200 250 300 350 - by Bioz Stars, 2026-11
    90/100 stars

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    Cloning:

    Article Title: Zona Pellucida Protein 2 (ZP2) Is Expressed in Colon Cancer and Promotes Cell Proliferation
    Article Snippet: . Human tumor cell lines were cultured in DMEM/10% FCS under a humidified 5% CO 2 atmosphere at 37 °C. The following cell lines were used: A-172, A549, A64-CLS, Hela, HL-60, LNCaP, MCF-7, MG-63, PC-3, SaOs, and SW-480 from Cell Lines Service (Eppelheim, Germany); B-CPAP, BHY, CAL-62, COLO320HSR, H1184, H146, HT29, LoVo, SKN-MC, SW-403, and THP-1 from DSMZ (Braunschweig, Germany); FTC-133, U251-MG, and U373-MG from Sigma-Aldrich (Taufkirchen, Ge

    Plasmid Preparation:

    Article Title: Zona Pellucida Protein 2 (ZP2) Is Expressed in Colon Cancer and Promotes Cell Proliferation
    Article Snippet: . Human tumor cell lines were cultured in DMEM/10% FCS under a humidified 5% CO 2 atmosphere at 37 °C. The following cell lines were used: A-172, A549, A64-CLS, Hela, HL-60, LNCaP, MCF-7, MG-63, PC-3, SaOs, and SW-480 from Cell Lines Service (Eppelheim, Germany); B-CPAP, BHY, CAL-62, COLO320HSR, H1184, H146, HT29, LoVo, SKN-MC, SW-403, and THP-1 from DSMZ (Braunschweig, Germany); FTC-133, U251-MG, and U373-MG from Sigma-Aldrich (Taufkirchen, Ge



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    Expression level of PPARG downstream target CK20 in colorectal cancer cell lines. Colorectal cancer cell lines HT29 and SW403 were treated with the PPARG agonists pioglitazone, rosiglitazone and siPPARG. After incubation for 48 hours, the protein expression level of the PPARG downstream target CK20 was measured using immunoblotting

    Journal: BMC Cancer

    Article Title: PPARG activation promotes the proliferation of colorectal cancer cell lines and enhances the antiproliferative effect of 5-fluorouracil

    doi: 10.1186/s12885-024-11985-5

    Figure Lengend Snippet: Expression level of PPARG downstream target CK20 in colorectal cancer cell lines. Colorectal cancer cell lines HT29 and SW403 were treated with the PPARG agonists pioglitazone, rosiglitazone and siPPARG. After incubation for 48 hours, the protein expression level of the PPARG downstream target CK20 was measured using immunoblotting

    Article Snippet: Human CRC cell lines SW403 and HT29 were purchased from the German Collection of Microorganisms and Cell Culture (DSMZ, Braunschweig, Germany).

    Techniques: Expressing, Incubation, Western Blot

    Cell viability assays. Activation of PPARG promotes proliferation in CRC cell lines ( A ). Inhibition of PPARG reduces viability in CRC cell lines ( B ). siRNA-mediated gene suppression of PPARG reduces cell viability in SW403 ( C ) (Data is presented as average ± standard deviation; statistical significance is indicated as **** p < 0.0001, *** p < 0.001, ** p < 0.01, * p < 0.05, ns non-significant; for statistical testing the t-test and Wilcoxon-Rank test were performed, both showing equal significance levels for all comparisons)

    Journal: BMC Cancer

    Article Title: PPARG activation promotes the proliferation of colorectal cancer cell lines and enhances the antiproliferative effect of 5-fluorouracil

    doi: 10.1186/s12885-024-11985-5

    Figure Lengend Snippet: Cell viability assays. Activation of PPARG promotes proliferation in CRC cell lines ( A ). Inhibition of PPARG reduces viability in CRC cell lines ( B ). siRNA-mediated gene suppression of PPARG reduces cell viability in SW403 ( C ) (Data is presented as average ± standard deviation; statistical significance is indicated as **** p < 0.0001, *** p < 0.001, ** p < 0.01, * p < 0.05, ns non-significant; for statistical testing the t-test and Wilcoxon-Rank test were performed, both showing equal significance levels for all comparisons)

    Article Snippet: Human CRC cell lines SW403 and HT29 were purchased from the German Collection of Microorganisms and Cell Culture (DSMZ, Braunschweig, Germany).

    Techniques: Activation Assay, Inhibition, Standard Deviation

    PPARG activation increases chemotherapy sensitivity of 5-Fluorouracil. Dose-response-curves for 5-Fluorouracil in cell lines HT29 and SW403 after treatment with the PPARG agonists pioglitazone and rosiglitazone, as well as the PPARG inhibitor GW9662 (statistical test results are shown in Table )

    Journal: BMC Cancer

    Article Title: PPARG activation promotes the proliferation of colorectal cancer cell lines and enhances the antiproliferative effect of 5-fluorouracil

    doi: 10.1186/s12885-024-11985-5

    Figure Lengend Snippet: PPARG activation increases chemotherapy sensitivity of 5-Fluorouracil. Dose-response-curves for 5-Fluorouracil in cell lines HT29 and SW403 after treatment with the PPARG agonists pioglitazone and rosiglitazone, as well as the PPARG inhibitor GW9662 (statistical test results are shown in Table )

    Article Snippet: Human CRC cell lines SW403 and HT29 were purchased from the German Collection of Microorganisms and Cell Culture (DSMZ, Braunschweig, Germany).

    Techniques: Activation Assay

    IC50 value for 5-FU after treatment with the PPARG agonists pioglitazone, rosiglitazone and the PPARG inhibitor GW9662

    Journal: BMC Cancer

    Article Title: PPARG activation promotes the proliferation of colorectal cancer cell lines and enhances the antiproliferative effect of 5-fluorouracil

    doi: 10.1186/s12885-024-11985-5

    Figure Lengend Snippet: IC50 value for 5-FU after treatment with the PPARG agonists pioglitazone, rosiglitazone and the PPARG inhibitor GW9662

    Article Snippet: Human CRC cell lines SW403 and HT29 were purchased from the German Collection of Microorganisms and Cell Culture (DSMZ, Braunschweig, Germany).

    Techniques: Standard Deviation, Control