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es2 ovarian cancer cell line atcc crl 1978 human  (ATCC)


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    ATCC es2 ovarian cancer cell line atcc crl 1978 human
    Es2 Ovarian Cancer Cell Line Atcc Crl 1978 Human, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1241 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/es2+ovarian+cancer+cell+line+atcc+crl+1978+human/ES-2/pmc10920785__41467_2024_46358_MOESM1_ESM-52-39-44
    Average 97 stars, based on 1241 article reviews
    es2 ovarian cancer cell line atcc crl 1978 human - by Bioz Stars, 2026-09
    97/100 stars

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    Article Title: Comprehensive multi-omics analysis reveals WEE1 as a synergistic lethal target with hyperthermia through CDK1 super-activation
    Article Snippet: Cell lines Catalog Identifier Human: HOC7 ovarian cancer cell line MDACC 's characterized Cell Line Core N/A Human: OVCAR8 ovarian cancer cell line MDACC 's characterized Cell Line Core N/A Human: A2780 ovarian cancer cell line Procell HYC3417 Human: ES2 ovarian cancer cell line ATCC CRL-1978 Human: SKOV3 ovarian cancer cell line ATCC HTB-77 Human: OVCAR3 ovarian cancer cell line ATCC HTB-161 Human: Caov3 ovarian cancer cell line ATCC HTB-75 Human: OV90 ovarian cancer cell line ATCC CRL-11732 Human: TOV-112D ovarian cancer cell line ATCC CRL-3593 Human: TOV-21G ovarian cancer cell line ATCC CRL-3577 Human: HacaT epidermal keratinocyte ATCC PCS-200-011 Human: HUVEC umbilical vein endothelial cells ATCC PCS-100-010 Human: IOSE80 ovarian surface epithelium cell line Cellosaurus CVCL_5546 Mouse: ID8 ovarian cancer cell line K. Roby’ lab N/A Mouse: CT26 colon carcinoma cell line ATCC CRL-2638 Mouse: MC38 colon adenocarcinoma cell line MDACC 's characterized Cell Line Core N/A Supplementary Table 3: The inhibitors used in this study.



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    ATCC es2 ovarian cancer cell line atcc crl 1978 human
    Es2 Ovarian Cancer Cell Line Atcc Crl 1978 Human, 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
    https://www.bioz.com/product/es2+ovarian+cancer+cell+line+atcc+crl+1978+human/ES-2/pmc10920785__41467_2024_46358_MOESM1_ESM-52-39-44
    Average 97 stars, based on 1 article reviews
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    ATCC human epithelial ovarian cancer cell lines es2
    Figure 2. miR‑28‑5p promotes the progression of cell cycle and proliferation and inhibits apoptosis in ovarian cancer cells. (A) The ability of cell proliferation was detected by clonal colony forming experiment in <t>ES2</t> and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or negative control (NC) respectively (**P<0.01). (B) MTT assay was performed to determine cell proliferation ability in ES2 and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or NC respectively. The values of expression level are represented by the mean percent of means ± SD (n=3, **P<0.01). (C) The cell cycle distribution was detected by flow cytometry. (D) Ovarian cancer cells were transfected with miR‑28‑5p mimic, inhibitor or NC and cell apoptosis was detected by Annexin Ⅴ-FITC/PI staining (***P<0.001).
    Human Epithelial Ovarian Cancer Cell Lines Es2, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/es2+ovarian+cancer+cell+line+atcc+crl+1978+human/ES-2%3B+Ovarian+Carcinoma%3B+Human/pm28350078-51-0-10
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    ATCC human ovarian cancer cell line es2
    Figure 2. miR‑28‑5p promotes the progression of cell cycle and proliferation and inhibits apoptosis in ovarian cancer cells. (A) The ability of cell proliferation was detected by clonal colony forming experiment in <t>ES2</t> and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or negative control (NC) respectively (**P<0.01). (B) MTT assay was performed to determine cell proliferation ability in ES2 and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or NC respectively. The values of expression level are represented by the mean percent of means ± SD (n=3, **P<0.01). (C) The cell cycle distribution was detected by flow cytometry. (D) Ovarian cancer cells were transfected with miR‑28‑5p mimic, inhibitor or NC and cell apoptosis was detected by Annexin Ⅴ-FITC/PI staining (***P<0.001).
    Human Ovarian Cancer Cell Line Es2, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/es2+ovarian+cancer+cell+line+atcc+crl+1978+human/ES-2%3B+Ovarian+Carcinoma%3B+Human/pmc03991758-144-0-9
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    Figure 2. miR‑28‑5p promotes the progression of cell cycle and proliferation and inhibits apoptosis in ovarian cancer cells. (A) The ability of cell proliferation was detected by clonal colony forming experiment in ES2 and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or negative control (NC) respectively (**P<0.01). (B) MTT assay was performed to determine cell proliferation ability in ES2 and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or NC respectively. The values of expression level are represented by the mean percent of means ± SD (n=3, **P<0.01). (C) The cell cycle distribution was detected by flow cytometry. (D) Ovarian cancer cells were transfected with miR‑28‑5p mimic, inhibitor or NC and cell apoptosis was detected by Annexin Ⅴ-FITC/PI staining (***P<0.001).

    Journal: International journal of oncology

    Article Title: miR-28-5p promotes the development and progression of ovarian cancer through inhibition of N4BP1.

    doi: 10.3892/ijo.2017.3915

    Figure Lengend Snippet: Figure 2. miR‑28‑5p promotes the progression of cell cycle and proliferation and inhibits apoptosis in ovarian cancer cells. (A) The ability of cell proliferation was detected by clonal colony forming experiment in ES2 and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or negative control (NC) respectively (**P<0.01). (B) MTT assay was performed to determine cell proliferation ability in ES2 and SKOV3 transfected with miR‑28‑5p mimic, inhibitor or NC respectively. The values of expression level are represented by the mean percent of means ± SD (n=3, **P<0.01). (C) The cell cycle distribution was detected by flow cytometry. (D) Ovarian cancer cells were transfected with miR‑28‑5p mimic, inhibitor or NC and cell apoptosis was detected by Annexin Ⅴ-FITC/PI staining (***P<0.001).

    Article Snippet: Human epithelial ovarian cancer cell lines ES2 were obtained from American Type Culture Collection (ATCC, Manassas, VA, USA) and SKOV3 cells were purchased from College of Life Science, Hunan Normal University, China.

    Techniques: Transfection, Negative Control, MTT Assay, Expressing, Flow Cytometry, Staining

    Figure 3. miR‑28‑5p expression accelerates migration and invasion ability of ovarian cancer cells. (A) The migration ability of ES2 and SKOV3 cells trans- fected with miR‑28‑5p mimic, inhibitor or NC were measured by wound healing assay at 0, 24 and 48 h respectively. (B) The migration assays of ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC respectively were performed. Magnification, x200; scale bars, 10 µm (**P<0.01). (C) The invasion assays of ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC respectively were performed. Magnification, x200; scale bars, 10 µm (**P<0.01).

    Journal: International journal of oncology

    Article Title: miR-28-5p promotes the development and progression of ovarian cancer through inhibition of N4BP1.

    doi: 10.3892/ijo.2017.3915

    Figure Lengend Snippet: Figure 3. miR‑28‑5p expression accelerates migration and invasion ability of ovarian cancer cells. (A) The migration ability of ES2 and SKOV3 cells trans- fected with miR‑28‑5p mimic, inhibitor or NC were measured by wound healing assay at 0, 24 and 48 h respectively. (B) The migration assays of ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC respectively were performed. Magnification, x200; scale bars, 10 µm (**P<0.01). (C) The invasion assays of ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC respectively were performed. Magnification, x200; scale bars, 10 µm (**P<0.01).

    Article Snippet: Human epithelial ovarian cancer cell lines ES2 were obtained from American Type Culture Collection (ATCC, Manassas, VA, USA) and SKOV3 cells were purchased from College of Life Science, Hunan Normal University, China.

    Techniques: Expressing, Migration, Wound Healing Assay, Transfection

    Figure 4. miR‑28‑5p regulates F-actin, E-cadherin, and vimentin expression. (A) Western blot analysis detected the expression level of F-actin in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC. GAPDH was used as a protein-loading control. (B) The expression levels of E-cadherin and vimentin were measured by western blot analysis in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC.

    Journal: International journal of oncology

    Article Title: miR-28-5p promotes the development and progression of ovarian cancer through inhibition of N4BP1.

    doi: 10.3892/ijo.2017.3915

    Figure Lengend Snippet: Figure 4. miR‑28‑5p regulates F-actin, E-cadherin, and vimentin expression. (A) Western blot analysis detected the expression level of F-actin in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC. GAPDH was used as a protein-loading control. (B) The expression levels of E-cadherin and vimentin were measured by western blot analysis in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC.

    Article Snippet: Human epithelial ovarian cancer cell lines ES2 were obtained from American Type Culture Collection (ATCC, Manassas, VA, USA) and SKOV3 cells were purchased from College of Life Science, Hunan Normal University, China.

    Techniques: Expressing, Western Blot, Transfection, Control

    Figure 5. miR‑28‑5p downregulates N4BP1 expression in human ovarian cancer. (A) Representative images of N4BP1 immunohistochemical staining in ovarian cancer tissues and adjacent ovarian tissues, original magnification, x400. (B) miR‑28‑5p inhibited the mRNA expression level of N4BP1 in ES2 cells. The mRNA expression level of N4BP1 was detected by qRT-PCR in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC. (C) The expression level of N4BP1 was detected by western blot analysis in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC.

    Journal: International journal of oncology

    Article Title: miR-28-5p promotes the development and progression of ovarian cancer through inhibition of N4BP1.

    doi: 10.3892/ijo.2017.3915

    Figure Lengend Snippet: Figure 5. miR‑28‑5p downregulates N4BP1 expression in human ovarian cancer. (A) Representative images of N4BP1 immunohistochemical staining in ovarian cancer tissues and adjacent ovarian tissues, original magnification, x400. (B) miR‑28‑5p inhibited the mRNA expression level of N4BP1 in ES2 cells. The mRNA expression level of N4BP1 was detected by qRT-PCR in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC. (C) The expression level of N4BP1 was detected by western blot analysis in ES2 and SKOV3 cells transfected with miR‑28‑5p mimic, inhibitor or NC.

    Article Snippet: Human epithelial ovarian cancer cell lines ES2 were obtained from American Type Culture Collection (ATCC, Manassas, VA, USA) and SKOV3 cells were purchased from College of Life Science, Hunan Normal University, China.

    Techniques: Expressing, Immunohistochemical staining, Staining, Quantitative RT-PCR, Transfection, Western Blot