human ovarian cancer cell line es Search Results


human granulosa cells (kgn  (Procell Inc)
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Procell Inc human granulosa cells (kgn
Human Granulosa Cells (Kgn, supplied by Procell Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ovarian surface epithelial cell line (hose, known hosepic  (ScienCell)
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ScienCell human ovarian surface epithelial cell line (hose, known hosepic
Human Ovarian Surface Epithelial Cell Line (Hose, Known Hosepic, supplied by ScienCell, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ovarian surface epithelial cell line (hose, known hosepic - by Bioz Stars, 2026-03
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human ovarian surface epithelial cells (hosepic)  (iCell Bioscience Inc)
90
iCell Bioscience Inc human ovarian surface epithelial cells (hosepic)
Human Ovarian Surface Epithelial Cells (Hosepic), supplied by iCell Bioscience Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human ovarian surface epithelial cells (hosepic)/product/iCell Bioscience Inc
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human ovarian cancer adenocarcinoma cell line skov3  (Tsang MD Inc)
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Tsang MD Inc human ovarian cancer adenocarcinoma cell line skov3
Human Ovarian Cancer Adenocarcinoma Cell Line Skov3, supplied by Tsang MD Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ovarian cancer adenocarcinoma cell line skov3 - by Bioz Stars, 2026-03
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human ovarian immortalized cell line hose11‑12  (Procell Inc)
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Procell Inc human ovarian immortalized cell line hose11‑12
Human Ovarian Immortalized Cell Line Hose11‑12, supplied by Procell Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ovarian immortalized cell line hose11‑12 - by Bioz Stars, 2026-03
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human ovarian epithelial cell line (t80 cells)  (China Center for Type Culture Collection)
90
China Center for Type Culture Collection human ovarian epithelial cell line (t80 cells)
Human Ovarian Epithelial Cell Line (T80 Cells), supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human ovarian epithelial cell line (t80 cells)/product/China Center for Type Culture Collection
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human ovarian epithelial cell line (t80 cells) - by Bioz Stars, 2026-03
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human ovarian cancer cell lines  (Korean Cell Line Bank)
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Korean Cell Line Bank human ovarian cancer cell lines
Human Ovarian Cancer Cell Lines, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ovarian cancer cell lines - by Bioz Stars, 2026-03
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skov3  (National Centre for Cell Science)
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National Centre for Cell Science skov3
Annexin-V FITC/PI staining of apoptosis at 24 h of incubation. (A) <t>SKOV3-CisR</t> control, (B) A2780-CisR cells, (C) A2780-CisR control, (D) MELS treated SKOV3-CisR cells.
Skov3, supplied by National Centre for Cell Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/skov3/product/National Centre for Cell Science
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skov3 - by Bioz Stars, 2026-03
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immortalized human ovarian surface epithelial cell line hose #t1074  (Applied Biological Materials Inc)
90
Applied Biological Materials Inc immortalized human ovarian surface epithelial cell line hose #t1074
MEG3 modulation affected proliferation and clonogenic capability of high-grade serous ovarian cancer (HGSOC) cells. ( A ) Relative MEG3 expression and ( B ) relative MEG3 subcellular localization assessed by RT-qPCR analysis in a panel of HGSOC cell lines as well as in HOSE (Human ovarian surface <t>epithelial</t> cells) and FT194 (Fallopian Tube epithelial cells). Data from total RNA are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using FT194 as a reference sample. Relative MEG3 expression in nucleus vs. cytoplasm is expressed as Log2FC values calculated with the ΔCt method and compared to FT194 cells; positive values represent nuclear enrichment. ( C ) Relative MEG3 expression assessed by RT-qPCR analysis in HEY and PEO1 cells (HGSOC cell lines) transiently transfected with pMEG3 (MEG3 expression plasmid) and with pcDNA (empty vector). Data are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using pcDNA as reference sample. ( D ) Bar chart representing proliferation assay for HEY-pMEG3 and PEO1-pMEG3 cells compared to respective control cells. Viable cells were counted at 24, 48, and 72 h from transfection. The mean cell proliferation at time x (Tx) was expressed as average percentage increase relative to T = 0 h (T0). ( E ) Clonogenic assay. Bar charts represent differences of clonogenic capability in MEG3 overexpressing cells with respect to control cells and representative pictures of clonogenic assays. For all experiments, bars and error bars refer to mean and SEM (standard error of the mean) of three experiments. To establish statistically significant differences, unpaired t -test was carried out: * p < 0.05; ** p < 0.01.
Immortalized Human Ovarian Surface Epithelial Cell Line Hose #T1074, supplied by Applied Biological Materials Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/immortalized human ovarian surface epithelial cell line hose #t1074/product/Applied Biological Materials Inc
Average 90 stars, based on 1 article reviews
immortalized human ovarian surface epithelial cell line hose #t1074 - by Bioz Stars, 2026-03
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human ovarian cancer cell lines ov56 and cov362  (DS Pharma Biomedical)
90
DS Pharma Biomedical human ovarian cancer cell lines ov56 and cov362
MEG3 modulation affected proliferation and clonogenic capability of high-grade serous ovarian cancer (HGSOC) cells. ( A ) Relative MEG3 expression and ( B ) relative MEG3 subcellular localization assessed by RT-qPCR analysis in a panel of HGSOC cell lines as well as in HOSE (Human ovarian surface <t>epithelial</t> cells) and FT194 (Fallopian Tube epithelial cells). Data from total RNA are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using FT194 as a reference sample. Relative MEG3 expression in nucleus vs. cytoplasm is expressed as Log2FC values calculated with the ΔCt method and compared to FT194 cells; positive values represent nuclear enrichment. ( C ) Relative MEG3 expression assessed by RT-qPCR analysis in HEY and PEO1 cells (HGSOC cell lines) transiently transfected with pMEG3 (MEG3 expression plasmid) and with pcDNA (empty vector). Data are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using pcDNA as reference sample. ( D ) Bar chart representing proliferation assay for HEY-pMEG3 and PEO1-pMEG3 cells compared to respective control cells. Viable cells were counted at 24, 48, and 72 h from transfection. The mean cell proliferation at time x (Tx) was expressed as average percentage increase relative to T = 0 h (T0). ( E ) Clonogenic assay. Bar charts represent differences of clonogenic capability in MEG3 overexpressing cells with respect to control cells and representative pictures of clonogenic assays. For all experiments, bars and error bars refer to mean and SEM (standard error of the mean) of three experiments. To establish statistically significant differences, unpaired t -test was carried out: * p < 0.05; ** p < 0.01.
Human Ovarian Cancer Cell Lines Ov56 And Cov362, supplied by DS Pharma Biomedical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human ovarian cancer cell lines ov56 and cov362/product/DS Pharma Biomedical
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human ovarian cancer cell lines ov56 and cov362 - by Bioz Stars, 2026-03
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human cancer cell line ovcar-3  (China Center for Type Culture Collection)
90
China Center for Type Culture Collection human cancer cell line ovcar-3
MEG3 modulation affected proliferation and clonogenic capability of high-grade serous ovarian cancer (HGSOC) cells. ( A ) Relative MEG3 expression and ( B ) relative MEG3 subcellular localization assessed by RT-qPCR analysis in a panel of HGSOC cell lines as well as in HOSE (Human ovarian surface <t>epithelial</t> cells) and FT194 (Fallopian Tube epithelial cells). Data from total RNA are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using FT194 as a reference sample. Relative MEG3 expression in nucleus vs. cytoplasm is expressed as Log2FC values calculated with the ΔCt method and compared to FT194 cells; positive values represent nuclear enrichment. ( C ) Relative MEG3 expression assessed by RT-qPCR analysis in HEY and PEO1 cells (HGSOC cell lines) transiently transfected with pMEG3 (MEG3 expression plasmid) and with pcDNA (empty vector). Data are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using pcDNA as reference sample. ( D ) Bar chart representing proliferation assay for HEY-pMEG3 and PEO1-pMEG3 cells compared to respective control cells. Viable cells were counted at 24, 48, and 72 h from transfection. The mean cell proliferation at time x (Tx) was expressed as average percentage increase relative to T = 0 h (T0). ( E ) Clonogenic assay. Bar charts represent differences of clonogenic capability in MEG3 overexpressing cells with respect to control cells and representative pictures of clonogenic assays. For all experiments, bars and error bars refer to mean and SEM (standard error of the mean) of three experiments. To establish statistically significant differences, unpaired t -test was carried out: * p < 0.05; ** p < 0.01.
Human Cancer Cell Line Ovcar 3, supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human cancer cell line ovcar-3/product/China Center for Type Culture Collection
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human cancer cell line ovcar-3 - by Bioz Stars, 2026-03
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human ovarian cancer cell lines a2780 cat#csc-c9491j  (Creative Bioarray Inc)
90
Creative Bioarray Inc human ovarian cancer cell lines a2780 cat#csc-c9491j
MEG3 modulation affected proliferation and clonogenic capability of high-grade serous ovarian cancer (HGSOC) cells. ( A ) Relative MEG3 expression and ( B ) relative MEG3 subcellular localization assessed by RT-qPCR analysis in a panel of HGSOC cell lines as well as in HOSE (Human ovarian surface <t>epithelial</t> cells) and FT194 (Fallopian Tube epithelial cells). Data from total RNA are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using FT194 as a reference sample. Relative MEG3 expression in nucleus vs. cytoplasm is expressed as Log2FC values calculated with the ΔCt method and compared to FT194 cells; positive values represent nuclear enrichment. ( C ) Relative MEG3 expression assessed by RT-qPCR analysis in HEY and PEO1 cells (HGSOC cell lines) transiently transfected with pMEG3 (MEG3 expression plasmid) and with pcDNA (empty vector). Data are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using pcDNA as reference sample. ( D ) Bar chart representing proliferation assay for HEY-pMEG3 and PEO1-pMEG3 cells compared to respective control cells. Viable cells were counted at 24, 48, and 72 h from transfection. The mean cell proliferation at time x (Tx) was expressed as average percentage increase relative to T = 0 h (T0). ( E ) Clonogenic assay. Bar charts represent differences of clonogenic capability in MEG3 overexpressing cells with respect to control cells and representative pictures of clonogenic assays. For all experiments, bars and error bars refer to mean and SEM (standard error of the mean) of three experiments. To establish statistically significant differences, unpaired t -test was carried out: * p < 0.05; ** p < 0.01.
Human Ovarian Cancer Cell Lines A2780 Cat#Csc C9491j, supplied by Creative Bioarray Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human ovarian cancer cell lines a2780 cat#csc-c9491j/product/Creative Bioarray Inc
Average 90 stars, based on 1 article reviews
human ovarian cancer cell lines a2780 cat#csc-c9491j - by Bioz Stars, 2026-03
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Image Search Results


Annexin-V FITC/PI staining of apoptosis at 24 h of incubation. (A) SKOV3-CisR control, (B) A2780-CisR cells, (C) A2780-CisR control, (D) MELS treated SKOV3-CisR cells.

Journal: Frontiers in Chemistry

Article Title: Lotus seed (Nelumbinis semen) extract: anticancer potential and chemoprofiling by in vitro , in silico and GC-MS studies

doi: 10.3389/fchem.2024.1505272

Figure Lengend Snippet: Annexin-V FITC/PI staining of apoptosis at 24 h of incubation. (A) SKOV3-CisR control, (B) A2780-CisR cells, (C) A2780-CisR control, (D) MELS treated SKOV3-CisR cells.

Article Snippet: Two human ovarian cancer cell lines, namely, SKOV3 and A2780, were obtained from the National Centre for Cell Sciences (NCCS), Pune, India.

Techniques: Staining, Incubation, Control

Flow cytometric cell cycle distribution analysis. (A) SKOV3-CisR control cells, (B) MELS treated SKOV3-CisR, (C) Control cells of A2780-CisR, (D) MELS treated A2780-CisR cells.

Journal: Frontiers in Chemistry

Article Title: Lotus seed (Nelumbinis semen) extract: anticancer potential and chemoprofiling by in vitro , in silico and GC-MS studies

doi: 10.3389/fchem.2024.1505272

Figure Lengend Snippet: Flow cytometric cell cycle distribution analysis. (A) SKOV3-CisR control cells, (B) MELS treated SKOV3-CisR, (C) Control cells of A2780-CisR, (D) MELS treated A2780-CisR cells.

Article Snippet: Two human ovarian cancer cell lines, namely, SKOV3 and A2780, were obtained from the National Centre for Cell Sciences (NCCS), Pune, India.

Techniques: Control

MEG3 modulation affected proliferation and clonogenic capability of high-grade serous ovarian cancer (HGSOC) cells. ( A ) Relative MEG3 expression and ( B ) relative MEG3 subcellular localization assessed by RT-qPCR analysis in a panel of HGSOC cell lines as well as in HOSE (Human ovarian surface epithelial cells) and FT194 (Fallopian Tube epithelial cells). Data from total RNA are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using FT194 as a reference sample. Relative MEG3 expression in nucleus vs. cytoplasm is expressed as Log2FC values calculated with the ΔCt method and compared to FT194 cells; positive values represent nuclear enrichment. ( C ) Relative MEG3 expression assessed by RT-qPCR analysis in HEY and PEO1 cells (HGSOC cell lines) transiently transfected with pMEG3 (MEG3 expression plasmid) and with pcDNA (empty vector). Data are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using pcDNA as reference sample. ( D ) Bar chart representing proliferation assay for HEY-pMEG3 and PEO1-pMEG3 cells compared to respective control cells. Viable cells were counted at 24, 48, and 72 h from transfection. The mean cell proliferation at time x (Tx) was expressed as average percentage increase relative to T = 0 h (T0). ( E ) Clonogenic assay. Bar charts represent differences of clonogenic capability in MEG3 overexpressing cells with respect to control cells and representative pictures of clonogenic assays. For all experiments, bars and error bars refer to mean and SEM (standard error of the mean) of three experiments. To establish statistically significant differences, unpaired t -test was carried out: * p < 0.05; ** p < 0.01.

Journal: Cancers

Article Title: Clinical Value of lncRNA MEG3 in High-Grade Serous Ovarian Cancer

doi: 10.3390/cancers12040966

Figure Lengend Snippet: MEG3 modulation affected proliferation and clonogenic capability of high-grade serous ovarian cancer (HGSOC) cells. ( A ) Relative MEG3 expression and ( B ) relative MEG3 subcellular localization assessed by RT-qPCR analysis in a panel of HGSOC cell lines as well as in HOSE (Human ovarian surface epithelial cells) and FT194 (Fallopian Tube epithelial cells). Data from total RNA are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using FT194 as a reference sample. Relative MEG3 expression in nucleus vs. cytoplasm is expressed as Log2FC values calculated with the ΔCt method and compared to FT194 cells; positive values represent nuclear enrichment. ( C ) Relative MEG3 expression assessed by RT-qPCR analysis in HEY and PEO1 cells (HGSOC cell lines) transiently transfected with pMEG3 (MEG3 expression plasmid) and with pcDNA (empty vector). Data are presented as Log2 fold change (Log2FC) values calculated with the ΔΔCt method, using pcDNA as reference sample. ( D ) Bar chart representing proliferation assay for HEY-pMEG3 and PEO1-pMEG3 cells compared to respective control cells. Viable cells were counted at 24, 48, and 72 h from transfection. The mean cell proliferation at time x (Tx) was expressed as average percentage increase relative to T = 0 h (T0). ( E ) Clonogenic assay. Bar charts represent differences of clonogenic capability in MEG3 overexpressing cells with respect to control cells and representative pictures of clonogenic assays. For all experiments, bars and error bars refer to mean and SEM (standard error of the mean) of three experiments. To establish statistically significant differences, unpaired t -test was carried out: * p < 0.05; ** p < 0.01.

Article Snippet: The immortalized human ovarian surface epithelial cell line (HOSE, #T1074) was purchased from Applied Biological Materials Inc. (ABM, Richmond, BC, Canada), whereas the immortalized Fallopian tube secretory epithelial cell line FT194 was kindly provided by Dr. MS Zannini, with the authorization of Dr. R Drapkin (Boston, MA, USA).

Techniques: Expressing, Quantitative RT-PCR, Transfection, Plasmid Preparation, Proliferation Assay, Control, Clonogenic Assay