GC cell lines (KATO-III, SGC-7901, BGC-823, HGC-27, AGS, NCI-N87, SNU-1 and SNU-16) and normal gastric epithelial cells (GES cells) were bought from the Shanghai Institute of Biochemistry and Cell Biology (Shanghai, China). All the cells were cultured at 37°C in a humidified atmosphere containing 5% of CO2 in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 10% of fetal bovine serum (FBS),100 U/ml penicillin, and 100 µg/ml streptomycin (all from Gibco, Invitrogen Life Technologies, Carlsbad, CA, USA).
Snu 1
Manufactured by Shanghai Institute of Biochemistry and Cell Biology
Sourced in China
The SNU-1 is a laboratory instrument designed for the analysis of biological samples. It is capable of performing high-throughput screening and data acquisition. The core function of the SNU-1 is to enable efficient and accurate measurement of various biochemical and cellular parameters.
Automatically generated - may contain errors
Lab products found in correlation
Penicillin, by Thermo Fisher Scientific (2 mentions)
Streptomycin, by Thermo Fisher Scientific (2 mentions)
Fetal bovine serum (fbs), by Thermo Fisher Scientific (2 mentions)
Sgc 7901, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Kato 3, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Nci n87, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Snu 16, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Ges cells, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Hgc27, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Bgc 823, by Shanghai Institute of Biochemistry and Cell Biology (2 mentions)
Dulbecco s modified eagle s medium dmem, by Thermo Fisher Scientific (1 mentions)
Dulbecco s modi ed eagle s medium dmem, by Thermo Fisher Scientific (1 mentions)
2 protocols using snu 1
1
Cultivation of Gastric Cell Lines
2
Gastric Cancer Tissue Samples and Cell Lines
Check if the same lab product or an alternative is used in the 5 most similar protocols
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Primary GC tissue samples and adjacent normal tissues were obtained from 40 patients who underwent surgical resection at the Second A liated Hospital of Nanchang University. None of the patients had received preoperative chemotherapy, radiotherapy, or other anticancer modalities. After the resection, the tissue samples were immediately frozen in liquid nitrogen and, then, stored in liquid nitrogen until subsequent treatment and analysis. Eight GC cell lines-KATO-III, SGC-7901, BGC-823, HGC-27, AGS, NCI-N87, SNU-1, and SNU-16-as well as normal gastric cells (GES cells) were bought from the Shanghai Institute of Biochemistry and Cell Biology (Shanghai, China). All the cells were cultured at 37°C in a humidi ed atmosphere containing 5% of CO2 in Dulbecco's Modi ed Eagle's Medium (DMEM) supplemented with 10% of fetal bovine serum (FBS),100 U/ml penicillin, and 100 µg/ml streptomycin (all from Gibco, Invitrogen Life Technologies, Carlsbad, CA, USA).
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