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The SW1116 is a centrifuge rotor designed for use with Thermo Fisher Scientific's line of high-speed centrifuges. It is capable of achieving maximum speeds up to 16,000 rpm and can accommodate sample volumes up to 1.5 mL. The rotor is constructed of durable materials and is designed for reliable performance in a variety of laboratory applications.

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18 protocols using sw1116

1

Culturing Colon Cell Lines

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Human colon cancer cell lines HT29, SW1116, SW480 and normal human colon epithelial cell line NCM460 were purchased from Institute of Biochemistry and Cell Biology (Chinese Academy of Sciences, Shanghai, People’s Republic of China) and maintained in a Roswell Park Memorial Institute 1640 medium (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% (v/v) fetal bovine serum (FBS; Sigma-Aldrich Co, St Louis, MO, USA), 100 IU/mL penicillin and 100 mg/mL streptomycin (Shanghai Baoman Biotechnology Co., Ltd., People’s Republic of China), at 37°C in a humidified atmosphere containing 5% CO2.
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Colorectal Cancer Cell Lines Protocol

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Human CRC cell lines SW1116 and SW837 and normal human fibroblast BUD8 (CRL1554) were obtained from the American Type Culture Collection. SW1116 and SW837 cells were grown in Leibowitz-15 (L15; 90%; Gibco; Thermo Fisher Scientific, Inc.) containing 10% FBS in a non-CO2 incubator. CRL1554 cells were grown in DMEM (90%; Gibco; Thermo Fisher Scientific, Inc.) containing 10% FBS in a CO2 incubator. Penicillin/streptomycin (Sigma-Aldrich; Merck KGaA), gentamicin (Gibco; Thermo Fisher Scientific, Inc.), L-glutamine (Fluka; Biochemika™), and sodium hydrogen carbonate (BDH; GPR™) were added to all media during preparation. The PPCs were all obtained from Sigma-Aldrich (Merck KGaA), including betulinic acid (BetA), coumarin (Cmr), Cur, hesperetin (Hsp), homoharringtonine (HHG), indol-3-carbinol (IC3), irinotecan (Irt), Kmf, lycopene (Lyp), Que, Rsv, silibinin (Sil), sinigrin (Snn), and sulanidac (Sul). Sora was purchased from MedChemExpress.
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Colorectal Cancer Cell Line and Tissue Sample Analysis

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Cell lines and culture. Colorectal cancer cell lines SW1116 and HT29 and human umbilical vein endothelial cells (HUVECs) were all purchased from the American Type Culture Collection (ATCC; Manassas, VA, USA). SW1116 and HT29 cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum (FBS; both from Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA). HUVECs were cultured in endothelial cell medium (Invitrogen; Thermo Fisher Scientific, Inc.) supplemented with 5% FBS and 1% endothelial cell growth supplement (Invitrogen; Thermo Fisher Scientific, Inc.). All cells were cultured at 37˚C in 5% CO 2 .
Tissue samples. With the approval from the Review Board and Ethics Committee of the People's Hospital of Xintai City, 80 primary CRC specimens were selected from patients who had undergone surgery between January 2006 and December 2014 in the Xintai People's Hospital (Shandong, China). No patients had received chemotherapy, radiotherapy or immunomodulatory therapy prior to surgery.
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4

Detailed Culturing of Common Cancer Cell Lines

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The DLD1 (ATCC CCL-221), HCT116 (ATCC CCL-247), LoVo (ATCC CCL-229), SW620 (ATCC CCL-227), SW1116 (ATCC CCL-233) and 293T (ATCC CRL-11268) cell lines were purchased from American Type Culture Collection (ATCC). The TC71 patient-derived xenograft cell line was obtained from XENTECH (MRF reference: XTM-233_CXT-399/R5700).
DLD1, HCT116, LoVo, SW620 and SW1116 were cultured in RPMI-1640 medium (Invitrogen, Carlsbad, USA) with 10% fetal bovine serum (HyClone, USA) as routine. 293T was maintained in Dulbecco’s modified Eagle’s medium (Invitrogen, Carlsbad, USA) supplemented with 10% fetal bovine serum. TC71 was propagated in Advanced DMEM/F12 supplemented with 8% FBS, 1% antibiotics and 1% Glutamin. All cells were grown in a humidified incubator at 37 °C with 5% CO2. All the cell lines were authenticated 3 months before the beginning of the study based on viability and morphology by the suppliers. Cells have not been in culture for longer than 2 months.
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5

Culturing Human Colon Cell Lines

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Human colon epithelial FHC cells, and the human CRC cell lines SW1116 and HT29 were all purchased from the American Type Culture Collection (Manassas, VA, USA). SW1116 and HT29 cell lines were cultured in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS; both from Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) (11 (link),12 (link)). The FHC cell line was cultured in mixed medium including DMEM and Ham's F12 nutrient mixture, supplemented with 10% FBS. All cells were cultured at 37°C in 5% CO2.
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6

Culturing Colorectal Cancer Cell Lines

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The immortalized human colorectal epithelial cell line (FHC) and CRC cell lines HCT116, DLD-1, SW480, LOVO, HT29, and RKO were purchased from American Type Culture Collection (ATCC). SW1116 and SW620 cells were obtained from the Cell Resource Center, Shanghai Institute of Biochemistry and Cell Biology at the Chinese Academy of Sciences. All cells were cultivated in a humidified environment with 5% CO2 at 37 °C in recommended growth medium added with 10% fetal bovine serum. FHC cells: Dulbecco’s modified Eagle’s medium/F12 Medium (Gibco, USA); SW1116, SW620 and DLD-1 cells: RPMI-1640 Medium (Gibco, USA); HCT116 and HT29 cells: McCoy’s 5a Medium (Gibco, USA); SW480 cells: L-15 medium (Gibco, USA); LoVo cells: F-12K Medium (Gibco, USA).
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7

Colorectal Cancer Tissue Collection and Cell Culture

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Twenty pairs of fresh frozen CRC tissues (tumor and corresponding adjacent) were obtained from the Sun Yat-sen University Cancer Center (SYSUCC), Guangzhou, China, between December 2015 and June 2017. All samples were selected and confirmed histologically based on the following criteria: primary resection of the tumor with detailed follow-up data and no preoperative anticancer treatment. The human CRC cell lines (HCT116, SW480, HT29, LOVO, SW1116, SW640) and controlled cell line (HEK-293T) were obtained from the Chinese Academy of Sciences, Shanghai Institutes for Cell Resource Center. HCT116 and HT29 were maintained in McCoy's 5A with L-glutamine (HyClone, Logan, UT, USA). SW480 was cultured in incomplete Leibovitz's L-15 medium (KeyGEN, Nanjing, Jiangsu, China) media supplemented with 10% heat-inactivated fetal bovine serum (Gibco, Carlsbad, CA, USA). The LOVO, SW1116, SW640, and HEK-293T were supported with DMEM (Gibco, Carlsbad, CA, USA) with 10% heat-inactivated fetal bovine serum (Gibco, Carlsbad, CA, USA). Cells were grown in a humidified incubator at 37 °C with 5% CO2. This present study was approved by the Ethics Committee of Sun Yat-sen University Cancer Center (NO. L102012020000B). All participants were recruited after providing signed informed consent.
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8

Culturing Colorectal and Kidney Cell Lines

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Human colorectal cancer cell lines including LoVo, Caco-2, HT-29, HCT 116, SW480, SW620, SW1116 and Human kidney 293T cell were obtained from ATCC (Manassas, VA, USA). LoVo was maintained with F12K medium (SIGMA, USA); HT-29 and HCT 116 were maintained with McCoy's 5A (SIGMA, USA); SW480, SW620, and SW1116 were cultured in Leibovitz' L-15 (GIBCO, USA) with 10% FBS (GIBCO, USA); Caco-2 was cultured in MEM (GIBCO, USA) with 20% FBS (GIBCO, USA); 293T was maintained in DMEM (GIBCO, USA) with 10% FBS (GIBCO, USA). The SW480, SW620, and SW1116 were incubated at 37°C without CO2; the other cells were cultured in 37°C with 5% CO2.
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9

Cell Culture Conditions for Colorectal Cancer

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All cell lines were obtained from the American Type Culture Collection (ATCC) and grown under established conditions:3 (link), 56 (link) the HT29 human CRC cells cultured in McCoy’s 5A (Gibco, Grand Island, NY, USA) with 10% fetal bovine serum (Gibco); the human CRC cell lines, SW480 and SW1116, cultured in RPMI-1640 (Gibco) with 10% fetal bovine serum (Gibco).
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10

Cultivation of Colorectal Cancer Cell Lines

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The human CRC cell lines HCT 116, LoVo, SW1116, and SW620 were acquired from Shanghai Cell bank of Chinese Academy of Sciences (Shanghai, China), apart from the human colon epithelial cell line FHC which were from Kunming Cell bank of Chinese Academy of Sciences (Kunming, China). The cells were cultured in the respective recommended media and culture conditions: McCOY's 5A (SIGMA, USA) + 10% fetal bovine serum (FBS, GIBCO, USA) and 5% CO2 for HCT 116; Ham's F-12K Medium (Invitrogen, USA) + 10% FBS and 5% CO2 for LoVo; Leibovitz's L-15 Medium (GIBCO, USA) + 10% FBS (GIBCO, USA) and 100% air for SW1116, and SW620; RPMI-1640 (GIBCO, USA) + 10% FBS (GIBCO, USA) for FHC. The culture temperature was 37 ℃.
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