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Dulbecco s modified eagle high glucose medium

Manufactured by Biowest
Sourced in France

Dulbecco's modified eagle high-glucose medium is a cell culture medium that provides nutrients and supports the growth of various cell types. It is a commonly used medium in biological research and laboratory applications.

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2 protocols using dulbecco s modified eagle high glucose medium

1

HaCaT Cell Culture and Treatments

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HaCaT cells [27 (link)], obtained from ATCC, were cultured in full medium (FM) comprising Dulbecco’s modified eagle high-glucose medium (Biowest, Nuaillé, France), completed with 10% FBS (Thermo Fisher Scientific, Waltham, MA USA), 1000 units/mL penicillin, 1000 μg/mL streptomycin (Sigma-Aldrich, St Louis, MO, USA) and 1% l-glutamine (Biowest, Nuaillé, France), at 37 °C in a 7.5% CO2 controlled atmosphere. Where indicated, cells were changed to serum deprived medium (SS). TGF-β1 (PeproTech, Rocky Hill, NJ, USA) was inoculated at 2 ng/mL. For samples maintained continuously in the absence or presence of TGF-β, culture medium was refreshed every 24 h and new TGF-β1, if indicated, was inoculated. Epidermal Growth Factor (EGF; Sigma-Aldrich, St Louis, MO, USA) was supplemented at 10 ng/mL. Supplementation with FBS was achieved by introducing fresh FBS into SS samples up to a final 10% concentration, or 10% extra supplementation making up to 20% final when introduced to cells already in FM.
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2

HaCaT Cell Culture and Chronification

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HaCaT cells [47 (link)], obtained from ATCC, were cultured in full medium (FM) comprising Dulbecco’s modified eagle high-glucose medium (Biowest, Nuaillé, France), completed with 10% FBS (Thermo Fisher Scientific, Waltham, MA, USA), 1000 units/mL penicillin, 1000 μg/mL streptomycin (Sigma-Aldrich, St. Louis, MO, USA), and 1% l-glutamine (Biowest, Nuaillé, France), at 37 °C in a 7.5% CO2 controlled atmosphere. Chronification was as indicated in Liarte et al., 2020 [18 (link)]. Briefly, HaCaT cells at 50% subconfluency were changed to a serum-deprived medium (SS). While some of them were kept in this condition, others were stimulated with 2 ng/mL of TGF-β1 (PeproTech, Rocky Hill, NJ, USA). For samples maintained continuously in the absence or presence of TGF-β, a culture medium supplemented with 2 ng/mL of TGF-β1 was refreshed every 24 h. After 48 h of treatment, cells were denominated SS (serum-starved) or SSTC (serum-starved TGF-β chronic) cells [18 (link)], respectively. Then, cells were treated for the conditions stated in each experiment.
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