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The BGC803 is a laboratory equipment designed for the cultivation and isolation of anaerobic microorganisms. It provides a controlled environment with reduced oxygen levels to support the growth of anaerobic bacteria and other anaerobic organisms.

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8 protocols using bgc803

1

Gastric Cell Lines Culture Protocol

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We applied the normal human stomach epithelial cell line GES-1 (CBTCCCAS, Shanghai, China) and the human gastric adenocarcinoma cell lines AGS, SGC7901, BGC803, and BGC823 (ATCC, Manassas, VA, USA) in this study, and these cell lines were cultured in DMEM and RPMI-1640 (Invitrogen, Carlsbad, CA, USA), respectively at 37 °C in a humidified atmosphere with 5% CO2, which was supplemented with 10% fetal bovine serum (Hyclone, Logan, UT, USA), penicillin/streptomycin (1:100 dilution; Invitrogen), and 4 mM glutamine (Life Technologies, Gibco BRL).
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2

Culturing Human Gastric Cell Lines

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The normal human gastric mucosa cells (GES-1) and human GC cells (BGC-803, AGS, HGC-27, SGC-7901, and BGC-823) were obtained from ATCC (Shanghai, China) and cultured in McCoy’s 5a Medium (Gibco, Grand Island, NY, USA), supplemented with 10% fetal bovine serum (Gibco, sourced from Australia) and 1% streptomycin/penicillin, at a temperature of 37°C with 5% CO2.
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3

Plasmid Manipulation and Cell Culture Protocol

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Plasmid pAAV-IRES-ZsGreen was purchased from Addgene (Cambridge, MA, USA). DNA and RNA extraction kits, DNA fragment gel extraction kit, restriction enzymes, and E. coli DH5α were purchased from TaKaRa (Dalian, China). Trypsin, fetal bovine serum (FBS), and Dulbecco’s modified Eagle’s medium (DMEM) were obtained from Gibco BRL Co. (Grand Island, NY, USA). All primers were synthesized by Thermo Fisher (Hudson, NH, USA). Cell lines, including HepG2, A549, BGC-803, and human umbilical vein endothelial cells (HUVEC), were purchased from ATCC (Manassas, VA, USA). C57b1/6 mice, age 6–8 weeks, were purchased from Ensiweier Biotech (Chongqing, China). Anti-Adenovirus Type 5 E1A and Anti-BNIP3L/NIX antibodies were purchased from Abcam Biotech (Cambridge, MA, USA).
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4

Culturing Human Gastric Cell Lines

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Five human GC cell lines (AGS, MKN-45, BGC-803, MGC-823, HGC-27) and one human normal gastric mucosal epithelial cell line (GES-1) were purchased from the cell bank of the Chinese Academy of Sciences (Shanghai Cancer Institute, Shanghai, China) or the American Type Culture Collection (Gaithersburg, MD, USA). GC cells and GES-1 cells were grown in RPMI-1640 medium supplemented with 10% fetal bovine serum (both from Thermo Scientific, Shanghai, China) and 1% penicillin-streptomycin (Beijing Solaibo Technology, Beijing, China) in an incubator at 37°C and 5% CO2.
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5

Culturing Diverse Cell Lines

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Human GC cell lines NCI-N87, SGC7901, BGC823, BGC803, and AGS; human normal gastric epithelium cell line GES-1; human kidney epithelial cell line HEK293; human lung fibroblast CCL-153; and human endothelial cell line EC-304 were all purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). Cells were plated in tissue culture dishes and cultured in Dulbecco’s modified Eagle’s medium (DMEM; Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% (v/v) heat-inactivated fetal bovine serum (FBS; Hyclone, Logan, UT, USA) in a humidified 5% CO2 incubator (Thermo Fisher Scientific) at 37°C for 2–4 days until 80% confluence was reached. Before experiment treatment, cells were digested using 0.05% trypsin solution (Ameresco, Framingham, MA, USA) and seeded into 6-well or 96-well tissue culture plates.
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6

Gastric cell lines and normal cells

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GC cell lines (SGC7901, BGC823, BGC803, AGS, and MKN45) and normal human gastric mucosal cells (GES-1) were purchased from the American Type Culture Collection (ATCC, https://www.atcc.org/). All cells were cultured in RPMI-1640 supplemented with 10% fetal bovine serum (FBS), 100 U/mL streptomycin, and 100 μg/mL penicillin (Invitrogen, Carlsbad, CA, USA) under standard conditions (5% CO2 at 37 °C).
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7

Gastric Cancer Cell Line Cultivation

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The GC cell lines SGC7901, BGC803, AGS, MKN45, BGC823, MGC803, HGC27 and the gastric mucosal epithelial cell lines GES-1 were obtained from American Type Culture Collection (ATCC, Manassas, VA, USA). SGC7901, AGS, BGC823, MKN45, BGC803, MGC803, HGC27, and GES-1 cells were cultured in RPMI-1640 medium (Gibco, Grand Island, NY, USA). All media were supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin (Sigma-Aldrich, St Louis, MO, USA), and 100 mg/mL streptomycin (Sigma-Aldrich). Cycloheximide (CHX), proteasome inhibitor MG132, chloroquine diphosphate (CQ), and GSK-3β inhibitor CHIR-99021 were bought from Selleck Chemicals (Houston, TX, USA). Alkaline phosphatase (CIP) was obtained from Roche (Roche Applied Science, Indianapolis, IN, USA). The GSK-3β inhibitor LiCl was obtained from Sigma Aldrich.
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8

Culturing Gastric Cell Lines

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GC cell lines (AGS, NUGC4, MKN74 and BGC-803) and normal human gastric epithelial cell line GES-1 were from American Type Culture Collection (Manassas, VA, USA). These cells were cultured with ' 'Dulbecco's Modified Eagle medium (DMEM) (Gibco, Carlsbad, CA, USA) with 10% fetal bovine serum (FBS, Gibco), 100 U/mL penicillin, and 100 μg/mL streptomycin (Gibco) in 5% CO2 at 37 °C.
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