human stomach cancer cell line Search Results


90
clea japan inc nci-n87 cells (human stomach cancer cell strain)
Nci N87 Cells (Human Stomach Cancer Cell Strain), supplied by clea japan 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/product/human+stomach+cancer+cell+line/us08202879-651-0-21?v=clea+japan+inc
Average 90 stars, based on 1 article reviews
nci-n87 cells (human stomach cancer cell strain) - by Bioz Stars, 2026-07
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90
China Center for Type Culture Collection human stomach adenocarcinoma (ags) cell line
Viability of Chinese hamster ovary <t>(CHO)</t> cells in response to serum deprivation and oxidative stress. <t>CHO</t> <t>cells</t> were seeded in 12‐well plates at a density of 1.5 × 105 cells per well and grown for 24 h. Then cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium, serum free medium with or without 200 μM H2O2. In order to ensure that other nutrient limitations were not experienced, cells were fed fresh medium every 48 h. Cells were taken every 2 days and analyzed for cell viability using Annexin V/PI double staining. Error bars represent SD for each measurement.
Human Stomach Adenocarcinoma (Ags) Cell Line, 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/product/human+stomach+cancer+cell+line/pmc06999486-116-1-18?v=China+Center+for+Type+Culture+Collection
Average 90 stars, based on 1 article reviews
human stomach adenocarcinoma (ags) cell line - by Bioz Stars, 2026-07
90/100 stars
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Naomoto Corporation human stomach cancer cell line
Viability of Chinese hamster ovary <t>(CHO)</t> cells in response to serum deprivation and oxidative stress. <t>CHO</t> <t>cells</t> were seeded in 12‐well plates at a density of 1.5 × 105 cells per well and grown for 24 h. Then cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium, serum free medium with or without 200 μM H2O2. In order to ensure that other nutrient limitations were not experienced, cells were fed fresh medium every 48 h. Cells were taken every 2 days and analyzed for cell viability using Annexin V/PI double staining. Error bars represent SD for each measurement.
Human Stomach Cancer Cell Line, supplied by Naomoto Corporation, 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/product/human+stomach+cancer+cell+line/pm15905616-195-38-25?v=Naomoto+Corporation
Average 90 stars, based on 1 article reviews
human stomach cancer cell line - by Bioz Stars, 2026-07
90/100 stars
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Human Stomach Cancer Parental Stem Cell Expansion Media with Serum This product is also available without Serum Cat# M36127-54PES This product would require pre-coated flasks with Human Stomach (parental) Cancer Stem Cell Extra-cellular Matrix Cat#
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Human (Parental) Stomach Cancer Stem Cell Extracellular Matrix Human (Parental) Stomach Cancer Stem Cell Extra-cellular Matrix is essential for the growth and proliferation of Human (Parental) Stomach Cancer Stem Cells. This product requires Human (Parental)
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Human Stomach Cancer Stem Cell Serum Free Colony Forming Unit Media This Product is also available with Serum Cat# M36127-54CFS This product would require pre-coated flasks with Human Stomach Cancer Stem Cell Extra-cellular Matrix Cat#
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Human Stomach Cancer Stem Cell Complete Media with Serum. This product is also available without Serum Cat# M36127-54 This product would require pre-coated flasks with Human Stomach Cancer Stem Cell Extra-cellular Matrix Cat# E36127-54 and
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This product is a dual‐labeled stable pool in the designated cell type. This stable cell line expresses firefly luciferase and eGFP simultaneously. This cell line can be used in vitro for cancer cell line research
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Human Stomach Cancer Stem Cell Patient-Derived Xenografts [PDX] Celprogen defines patient-derived tumor grafts as explants established as models at low passage numbers (average mean of 6 passes removed from patient). They have not been grown
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Human (Parental) Stomach Cancer Stem Cell; Frozen Vial and Plated cells are available. Cells are only guaranteed with purchase of AcceGen Media and AcceGen Extra Cellular Matrix for appropriate cell culture, for 30 days from
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Human (Parental) Stomach Cancer Stem Cell Colony Forming Unit Complete Media with Serum This product is also available without Serum Cat# M36127-54PCF This product would require pre-coated flasks with Human (Parental) Stomach Cancer Stem Cell
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Human Stomach Cancer Stem Cell Serum Free Media. This Product is also available with Serum Cat# M36127-54S This product would require pre-coated flasks with Human Stomach Cancer Stem Cell Extra-cellular Matrix Cat# E36127-54 and Human
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Viability of Chinese hamster ovary (CHO) cells in response to serum deprivation and oxidative stress. CHO cells were seeded in 12‐well plates at a density of 1.5 × 105 cells per well and grown for 24 h. Then cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium, serum free medium with or without 200 μM H2O2. In order to ensure that other nutrient limitations were not experienced, cells were fed fresh medium every 48 h. Cells were taken every 2 days and analyzed for cell viability using Annexin V/PI double staining. Error bars represent SD for each measurement.

Journal: Engineering in Life Sciences

Article Title: Overexpression of GRP78 enhances survival of CHO cells in response to serum deprivation and oxidative stress

doi: 10.1002/elsc.201500152

Figure Lengend Snippet: Viability of Chinese hamster ovary (CHO) cells in response to serum deprivation and oxidative stress. CHO cells were seeded in 12‐well plates at a density of 1.5 × 105 cells per well and grown for 24 h. Then cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium, serum free medium with or without 200 μM H2O2. In order to ensure that other nutrient limitations were not experienced, cells were fed fresh medium every 48 h. Cells were taken every 2 days and analyzed for cell viability using Annexin V/PI double staining. Error bars represent SD for each measurement.

Article Snippet: The Chinese hamster ovary (CHO) cells, human stomach adenocarcinoma (AGS) cell line, and human hepatoma cell line HepG2 (China Center for Type Culture Collection, Wuhan, P. R. China) were cultured in Roswell Park Memorial Institute (RPMI) 1640 and DMEM medium (Gbico BRL, NY, USA) supplemented with 10% FBS (Sijiqing, Hangzhou, China) and 100 U/mL ampicillin, 100 mg/mL streptomycin in an incubator containing 5% CO 2 at 37°C (standard conditions).

Techniques: Cell Culture, Double Staining

Glucose‐regulated protein 78 (GRP78) engineering protected Chinese hamster ovary (CHO) cells against injury induced by H2O2. (A) Cells synchronized in serum‐free medium were treated with H2O2 at increasing concentration for 4 h and then cultured with 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT; 5 mg/mL) for 4 h. Bar graph represented the percentage of viable cells assayed by MTT. (B) The level of cleaved caspase‐3 in H2O2‐treated cells was detected by western blot (upper). The lower left bar graph represented densitometric analysis of GRP78 levels of the western blots and the lower right of cleaved caspase‐3. Data were mean values ± SD, n > 3.*p < 0.05,**p < 0.01,***p < 0.001, NS, nonsignificant difference versus negative control.

Journal: Engineering in Life Sciences

Article Title: Overexpression of GRP78 enhances survival of CHO cells in response to serum deprivation and oxidative stress

doi: 10.1002/elsc.201500152

Figure Lengend Snippet: Glucose‐regulated protein 78 (GRP78) engineering protected Chinese hamster ovary (CHO) cells against injury induced by H2O2. (A) Cells synchronized in serum‐free medium were treated with H2O2 at increasing concentration for 4 h and then cultured with 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT; 5 mg/mL) for 4 h. Bar graph represented the percentage of viable cells assayed by MTT. (B) The level of cleaved caspase‐3 in H2O2‐treated cells was detected by western blot (upper). The lower left bar graph represented densitometric analysis of GRP78 levels of the western blots and the lower right of cleaved caspase‐3. Data were mean values ± SD, n > 3.*p < 0.05,**p < 0.01,***p < 0.001, NS, nonsignificant difference versus negative control.

Article Snippet: The Chinese hamster ovary (CHO) cells, human stomach adenocarcinoma (AGS) cell line, and human hepatoma cell line HepG2 (China Center for Type Culture Collection, Wuhan, P. R. China) were cultured in Roswell Park Memorial Institute (RPMI) 1640 and DMEM medium (Gbico BRL, NY, USA) supplemented with 10% FBS (Sijiqing, Hangzhou, China) and 100 U/mL ampicillin, 100 mg/mL streptomycin in an incubator containing 5% CO 2 at 37°C (standard conditions).

Techniques: Concentration Assay, Cell Culture, Western Blot, Negative Control

Glucose‐regulated protein 78 (GRP78) engineering enhanced yields of TfR‐Ab and improved cell viability. Chinese hamster ovary (CHO) and CHO modified by GRP78 (CHO‐GRP78) cells were seeded in 12‐well plates at a density of 2 × 105 cells per well and transiently transfected with pOptiVEC™‐TOPO®/TfR‐Ab, followed by culturing with SFM4CHO™ medium. (A) The concentration of TfR‐Ab in the supernatant was detected by ELISA assay. (B) The quality of TfR‐Ab in the supernatant was evaluated by its binding ability with TfR+ HepG2 cells using flow cytometry (FCM). The bar graphs represented FCM analysis of mean fluorescence index (MFI). (C) Bar graph represented FCM analysis of the percentage viability of CHO and CHO‐GRP78 cells. (D) The viable cell numbers of CHO and CHO‐GRP78 cells were counted after Trypan blue staining. Data were mean values ± SD, n > 3.*p < 0.05,**p < 0.01,***p < 0.001 versus negative control.

Journal: Engineering in Life Sciences

Article Title: Overexpression of GRP78 enhances survival of CHO cells in response to serum deprivation and oxidative stress

doi: 10.1002/elsc.201500152

Figure Lengend Snippet: Glucose‐regulated protein 78 (GRP78) engineering enhanced yields of TfR‐Ab and improved cell viability. Chinese hamster ovary (CHO) and CHO modified by GRP78 (CHO‐GRP78) cells were seeded in 12‐well plates at a density of 2 × 105 cells per well and transiently transfected with pOptiVEC™‐TOPO®/TfR‐Ab, followed by culturing with SFM4CHO™ medium. (A) The concentration of TfR‐Ab in the supernatant was detected by ELISA assay. (B) The quality of TfR‐Ab in the supernatant was evaluated by its binding ability with TfR+ HepG2 cells using flow cytometry (FCM). The bar graphs represented FCM analysis of mean fluorescence index (MFI). (C) Bar graph represented FCM analysis of the percentage viability of CHO and CHO‐GRP78 cells. (D) The viable cell numbers of CHO and CHO‐GRP78 cells were counted after Trypan blue staining. Data were mean values ± SD, n > 3.*p < 0.05,**p < 0.01,***p < 0.001 versus negative control.

Article Snippet: The Chinese hamster ovary (CHO) cells, human stomach adenocarcinoma (AGS) cell line, and human hepatoma cell line HepG2 (China Center for Type Culture Collection, Wuhan, P. R. China) were cultured in Roswell Park Memorial Institute (RPMI) 1640 and DMEM medium (Gbico BRL, NY, USA) supplemented with 10% FBS (Sijiqing, Hangzhou, China) and 100 U/mL ampicillin, 100 mg/mL streptomycin in an incubator containing 5% CO 2 at 37°C (standard conditions).

Techniques: Modification, Transfection, Concentration Assay, Enzyme-linked Immunosorbent Assay, Binding Assay, Flow Cytometry, Fluorescence, Staining, Negative Control