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Sodium bicarbonate

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Sodium Bicarbonate is a versatile laboratory chemical used as a pH adjuster and buffer. It is a white, crystalline powder that dissolves in water to produce a slightly alkaline solution. Sodium Bicarbonate is commonly used to maintain specific pH levels in various laboratory applications and experiments.

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2 protocols using sodium bicarbonate

1

Culturing and Maintaining Human Cancer Cell Lines

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HCT116 (CCL-247™) and HT29 (HTB-38™) human colorectal and HepG2 (HB-8065™) human hepatocellular carcinoma cell lines were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). The HCT116 and HT29 cells were maintained in McCoy’s 5A medium +2.2 g/L Sodium Bicarbonate (HyClone Laboratories, Logan, UT, USA). HepG2 cells were maintained in Eagle’s minimum essential medium (EMEM). Both cell culture media were supplemented with 2 mM L-Glutamine (Lonza, Walkersville, MD, USA), 10% fetal calf serum (FCS) (HyClone Laboratories, Logan, UT, USA) and Penicillin/Streptomycin; 100 μg/ml each (Gibco, Grand Island, NY, USA). All cells were kept in a humidified atmosphere at 5% CO2 and 37°C.
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2

Cultivating Cancer Cell Lines for Assays

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The hepatocellular carcinoma cell lines Hep G2 and Hep 3B, the colorectal carcinoma cell line HT-29, and the pancreatic adenocarcinoma cell line Panc-1 were obtained from the American Type Culture Collection (ATCC®, Manassas, VA, USA). Catalog number and passage number are provided in the supplementary material. Hep G2 and Hep 3B cell lines were cultured in Eagle's Minimal Essential Medium (EMEM) +2 mM L-Glutamine (Lonza, Walkersville, MD, USA), HT-29 in Mc Coy's 5A + 1.5 mM L-Glutamine, +2.2 g/L Sodium Bicarbonate and Panc-1 in Dulbecco's Modified Essential Medium (DMEM) + 4.5 g/L D-Glucose, +2 mM L-Glutamine, +110 mg/L Sodium Pyruvate (HyClone Laboratories, Logan, UT, USA). All medias were supplemented with 10% fetal calf serum (FCS) (HyClone Laboratories, Logan, UT, USA) and Penicillin/Streptomycin; 100 μg/ml each (Gibco, Grand Island, NY, USA). Cells were cultured in a humidified atmosphere of 5% CO2 at 37 °C. For testing, cells were seeded in black walled, clear bottom 96 well plates (1 × 104 cells per well; cytotoxicity, caspase 3/7 activity, reactive oxygen species & TUNEL assay) or in 24 well plates for radioactive experiments (7.5 × 104 cells per well) one day prior to treatment and testing.
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