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The SNU-5 is a compact and versatile lab equipment designed for a range of scientific applications. It functions as a dedicated incubator, providing a controlled environment for cell culture, microbiological studies, and other temperature-sensitive experiments. The SNU-5 maintains precise temperature and atmospheric conditions to support the growth and development of various cell lines and microorganisms.

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51 protocols using snu 5

1

Curcumin Treatment of Cell Lines

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MCF-10A, HL60, SNU-5, LS180, BV2, CHME, and THP1 was purchased from ATCC (American Type Culture Collection) (Manassas, VA) was grown in RPMI media completed with 10% FBS, including penicillin G (70 mg/L), streptomycin (100 mg/L), and NaHCO3 (3.7 g/L) in an incubator at 37°C, 98% humidity, and 5% CO2. Treatment of cells with curcumin was dose- and time-dependent and curcumin was dissolved in DMSO (<0.1% DMSO).
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2

Establishment and Characterization of Gastric Cancer Cell Lines

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Establishment of tissue culture line SB.msgc-1 at our institution was previously reported [14 (link)]. Gastric cancer lines SNU-1, SNU-5, SNU-16, KATO III, AGS, NCI-N87, and BxPC-3 and HeLa cells were purchased from ATCC (American Type Culture Collection (ATCC), Manassas, VA). Antibodies for immunofluorescence studies included mouse anti-E-cadherin primary antibody (BD Transduction Laboratories, San Jose, CA), CEA/CD66e antibody (Cell Signaling, Danvers, MA), mouse IgG2a, κ (BD Biosciences, San Jose, CA), mouse (G3A1) mAb IgG1 isotype control (Cell Signaling, Danvers, MA), and Alexa Fluor ® 488 goat anti-mouse IgG (H + L) antibody (Life Technologies, Frederick, MD). Etoposide, mitoxantrone, and PI-103 were purchased from SelleckChem (Houston, TX).
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3

Cell Culture Protocol for Common Cell Lines

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Cell lines K‐562, SK‐BR‐3, MCF7, A‐431, and SNU‐5 were obtained from ATCC (Manassas, VA, USA) and cultured according to instructions provided.
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4

Gastric Cancer Cell Line Culture

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GC cell lines SNU‐5, HGC‐27, N87 and SGC‐7901 and the normal gastric mucosal cell line GES1 were purchased from ATCC (Manassas VA). RPMI1640 culture media (GIBCO‐BRL; Thermo Fisher Scientific, Waltham, MA) containing 100 U/ml streptomycin/penicillin and 10% fetal bovine serum (FBS) (Hyclone, USA) were placed in a thermostatic incubator containing 5% CO2 at saturated humidity at 37°C.
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5

Cell Culture Conditions Across Cell Lines

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All cell lines (HaCAT, LO2, CaES-17, EC109, MKN45, SNU-5, SW60, HepG2, and Hep3B) were purchased from ATCC cell bank. LO2 cells were cultured in Minimum Essential Medium (MEM) Eagles with Earle's Balanced Salts (MEM-EBSS). Other cells were cultured in DMEM medium (Gibco). Penicillin (100 U/mL), streptomycin (100 mg/mL), and 10% fetal bovine serum were added to the media. All cell lines grew in a humidified air containing 5% CO2 at 37 °C. Passage 10 cells were used in the experiments.
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6

Gastric Cancer Cell Line Cultivation

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The human GC cell lines AGS and NCI-N87 and the human normal gastric mucosal cell line GES-1 were obtained from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). The human GC cell lines Hs-746T and SNU-719 were purchased from Procell (Wuhan, China). The human GC cell line SNU-5 was obtained from ATCC. Cells were cultured in RPMI-1640 medium (Gibco, Grand Island, NY, United States) supplemented with 10% fetal bovine serum (FBS) (NBCS) (PAA Laboratories, Inc., Pasching, Austria) at 37°C in an atmosphere of 5% CO2.
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7

Gastric Cancer Cell Line Protocol

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GC samples were collected from patients who underwent surgery at Fudan University Shanghai Cancer Center between 2012 and 2013. The protocol was approved by the Clinical Research Ethics Committee of Fudan University, and the research was carried out according to the provisions of the Helsinki Declaration of 1975. All samples were obtained with the informed consent of the patients. The human GC cell line AGS (ATCC® CRL-1739™), SNU-1 (ATCC® CRL-5971™), SNU-5 (ATCC® CRL-5973™), SNU-16 (ATCC® CRL- 5974™), NCI-N87 (ATCC® CRL-5822™), and KATO III (ATCC® HTB-103™) were maintained in DMEM containing 10% fetal bovine serum. All cell lines were maintained in media containing penicillin (100 IU/ml) and streptomycin (100 mg/ml) at 37°C with 5% CO2. The miRNA mimics and inhibitors were purchased from Ambion (Austin, TX, USA).
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8

Gastric Cancer Cell Line Cultivation

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Gastric cancer cell lines-SNU-1, SNU-5, SNU-16, KATO-III and AGS, were procured from ATCC (Manassas, VA). All cell lines were grown in RPMI-1640 medium (Invitrogen; Carlsbad, CA) supplemented with 10% fetal bovine serum (FBS) and maintained in a humidified CO 2 incubator at 37 °C.
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9

Cultivation of Gastric Epithelial Cell Lines

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The human gastric epithelial cell line GES-1 was purchased from Beyotime Institute of Biotechnology (Suzhou, China). The GC cell lines AGS and SNU5 were obtained from ATCC. The GC cell line MKN45 was provided by Procell Life Science & Technology Co., Ltd. (Wuhan, China). GES-1, AGS, MKN45, and SNU5 cells were cultured in DMEM supplemented with 100 U/mL penicillin/streptomycin and 10% FBS at 37°C in the presence of 5% CO2.
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10

Gastric and Lung Cancer Cell Lines

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The human gastric cancer cell lines, HSC-39, HSC-43, HSC-59, HSC-60, HSC-64, HSC-44PE, 58As9, 58As1, and 44As3, have been described previously [40 (link),41 (link),42 (link),43 (link),44 (link)]. The human gastric cancer cell lines, MKN1, MKN7, MKN74, NUGC-4, KATO-III, MKN45, IM95, and human lung cancer cell line EBC-1 were obtained from the JCRB Cell Bank (Osaka, Japan). The human gastric cancer cell lines, NCI-N87 and SNU-5, human lung cancer cell line A549, and human mesothelial cell line Met5A were obtained from ATCC (Rockville, MD, USA). The human gastric cancer cell lines, GCIY, ECC12, H-111-TC, GSU, and KE-97, were provided by the RIKEN BRC through the National Bio-Resource Project of the MEXT, Japan (Ibaraki, Japan). These cells were maintained in RPMI 1640 medium (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% fetal bovine serum, 10 U/mL of penicillin, and 10 µg/mL of streptomycin at 37 °C in a humidified atmosphere containing 5% CO2. Mycoplasma contamination was tested using a MycoAlert Mycoplasma Detection Kit (Lonza, Basel, Switzerland).
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