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human ovarian cancer cell lines es 2  (ATCC)


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    ATCC human ovarian cancer cell lines es 2
    Human Ovarian Cancer Cell Lines Es 2, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1244 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ovarian+cancer+cell+line+es/ES-2/pm42150269-120-0-14
    Average 97 stars, based on 1244 article reviews
    human ovarian cancer cell lines es 2 - by Bioz Stars, 2026-10
    97/100 stars

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    other:

    Article Title: Quantification of Unencapsulated Drug in Target Tissues Demonstrates Pharmacological Properties and Therapeutic Effects of Liposomal Topotecan (FF-10850)
    Article Snippet: The human ovarian cancer cell line ES-2 was obtained from ATCC (Manassas, VA).

    Article Title: Quantification of Unencapsulated Drug in Target Tissues Demonstrates Pharmacological Properties and Therapeutic Effects of Liposomal Topotecan (FF-10850).
    Article Snippet: The human ovarian cancer cell line ES-2 was obtained from ATCC (Manassas, VA).



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    Fig. 6 PVRbbz CAR-T cells effectively killed multiple tumor cell lines even at low effector:target ratios and corroborated by cytokines release. A-L Cytotoxicity of PVRbbz CAR-T cells on PC3 (A and G), PANC1 (B and H), U20S (C and I), <t>ES2</t> (D and J), Huh7 (E and K) and MM.1S (F and L) cells at the indicated effector:target (E:T) ratios after 12 h of co-culturing. Cell Lysis was determined by luciferase and relative IVIS picture was shown. Two independent experiments were performed. M and N The concentrations of TNF-α (M) and IFN-γ (N) in supernatants from cytotoxicity assays at 1:1 effector:target after co-culture with tumor cells for 12 h were measured by ELISA kits. Three independent experiments were performed. Significance was calculated by two-way ANOVA. All error bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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    Fig. 6 PVRbbz CAR-T cells effectively killed multiple tumor cell lines even at low effector:target ratios and corroborated by cytokines release. A-L Cytotoxicity of PVRbbz CAR-T cells on PC3 (A and G), PANC1 (B and H), U20S (C and I), <t>ES2</t> (D and J), Huh7 (E and K) and MM.1S (F and L) cells at the indicated effector:target (E:T) ratios after 12 h of co-culturing. Cell Lysis was determined by luciferase and relative IVIS picture was shown. Two independent experiments were performed. M and N The concentrations of TNF-α (M) and IFN-γ (N) in supernatants from cytotoxicity assays at 1:1 effector:target after co-culture with tumor cells for 12 h were measured by ELISA kits. Three independent experiments were performed. Significance was calculated by two-way ANOVA. All error bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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    Fig. 6 PVRbbz CAR-T cells effectively killed multiple tumor cell lines even at low effector:target ratios and corroborated by cytokines release. A-L Cytotoxicity of PVRbbz CAR-T cells on PC3 (A and G), PANC1 (B and H), U20S (C and I), <t>ES2</t> (D and J), Huh7 (E and K) and MM.1S (F and L) cells at the indicated effector:target (E:T) ratios after 12 h of co-culturing. Cell Lysis was determined by luciferase and relative IVIS picture was shown. Two independent experiments were performed. M and N The concentrations of TNF-α (M) and IFN-γ (N) in supernatants from cytotoxicity assays at 1:1 effector:target after co-culture with tumor cells for 12 h were measured by ELISA kits. Three independent experiments were performed. Significance was calculated by two-way ANOVA. All error bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
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    Fig. 6 PVRbbz CAR-T cells effectively killed multiple tumor cell lines even at low effector:target ratios and corroborated by cytokines release. A-L Cytotoxicity of PVRbbz CAR-T cells on PC3 (A and G), PANC1 (B and H), U20S (C and I), <t>ES2</t> (D and J), Huh7 (E and K) and MM.1S (F and L) cells at the indicated effector:target (E:T) ratios after 12 h of co-culturing. Cell Lysis was determined by luciferase and relative IVIS picture was shown. Two independent experiments were performed. M and N The concentrations of TNF-α (M) and IFN-γ (N) in supernatants from cytotoxicity assays at 1:1 effector:target after co-culture with tumor cells for 12 h were measured by ELISA kits. Three independent experiments were performed. Significance was calculated by two-way ANOVA. All error bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001
    Human Ovarian Cancer Cell Line Es, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Fig. 6 PVRbbz CAR-T cells effectively killed multiple tumor cell lines even at low effector:target ratios and corroborated by cytokines release. A-L Cytotoxicity of PVRbbz CAR-T cells on PC3 (A and G), PANC1 (B and H), U20S (C and I), ES2 (D and J), Huh7 (E and K) and MM.1S (F and L) cells at the indicated effector:target (E:T) ratios after 12 h of co-culturing. Cell Lysis was determined by luciferase and relative IVIS picture was shown. Two independent experiments were performed. M and N The concentrations of TNF-α (M) and IFN-γ (N) in supernatants from cytotoxicity assays at 1:1 effector:target after co-culture with tumor cells for 12 h were measured by ELISA kits. Three independent experiments were performed. Significance was calculated by two-way ANOVA. All error bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001

    Journal: Genome medicine

    Article Title: Pan-cancer analysis identifies CD155 as a promising target for CAR-T cell therapy.

    doi: 10.1186/s13073-025-01490-0

    Figure Lengend Snippet: Fig. 6 PVRbbz CAR-T cells effectively killed multiple tumor cell lines even at low effector:target ratios and corroborated by cytokines release. A-L Cytotoxicity of PVRbbz CAR-T cells on PC3 (A and G), PANC1 (B and H), U20S (C and I), ES2 (D and J), Huh7 (E and K) and MM.1S (F and L) cells at the indicated effector:target (E:T) ratios after 12 h of co-culturing. Cell Lysis was determined by luciferase and relative IVIS picture was shown. Two independent experiments were performed. M and N The concentrations of TNF-α (M) and IFN-γ (N) in supernatants from cytotoxicity assays at 1:1 effector:target after co-culture with tumor cells for 12 h were measured by ELISA kits. Three independent experiments were performed. Significance was calculated by two-way ANOVA. All error bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001

    Article Snippet: Prostate cancer cell lines PC3, C4-2, DU145, multiple myeloma MM.1S cell line, chronic myeloid leukemia K562 cell line, osteosarcoma cell lines U20S and 143B, ovarian cancer cell line ES2 and OVCAR8, pancreatic cancer cell line PANC1 and CAPAN-2, lung cancer cell line H292, colorectal carcinoma cell line HT29 and murine melanoma cell line B16 F10 were obtained from the American Type Culture Collection (ATCC).

    Techniques: Lysis, Luciferase, Co-Culture Assay, Enzyme-linked Immunosorbent Assay