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Dulbecco s modified eagle medium low glucose dmem lg

Manufactured by Merck Group
Sourced in United States

Dulbecco's Modified Eagle Medium Low Glucose (DMEM-LG) is a cell culture medium formulation developed by Merck Group. It is a basal medium that provides essential nutrients and supplements required for the in vitro cultivation of various cell types. The low glucose concentration in DMEM-LG is a key feature that differentiates it from other DMEM formulations.

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2 protocols using dulbecco s modified eagle medium low glucose dmem lg

1

Culturing NIH 3T3 Mouse Fibroblasts

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Copper acetate monohydrate (molecular weight: 199.65 g mol−1) was purchased from Sigma Aldrich. Ethanol was purchased from Anal R NORMAPUR (UK). Trypsin-EDTA solution and Dulbecco's Modified Eagle Medium Low Glucose (DMEM-LG) was purchased from Sigma Aldrich USA. Fetal bovine serum (FBS) was acquired from Gibco. NIH 3T3 mouse embryonic fibroblast cell line was a gift from Interdisciplinary Research center in Biomedical materials (IRCBM), COMSATS University Islamabad, Lahore, Pakistan.
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2

Isolation of Wharton's Jelly Mesenchymal Stem Cells

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The present study was approved by the Biosafety Board at The University of Lahore, Lahore, Pakistan. Samples were collected after obtaining written informed consent from mothers and all samples were screened for the absence of hepatitis B virus, hepatitis C virus, and human immunodeficiency virus. Samples were collected in sterile tubes and transported to the tissue culture laboratory immediately after collection. WJMSCs were isolated from umbilical cords by an explant culturing method as we previously described.8 (link) Briefly, cord pieces were incubated in 3 mg/ml collagenase solution (Invitrogen, Carlsbad, CA, USA). After 3 h, Dulbecco's modified eagle medium-low glucose (DMEM LG) (Sigma Aldrich, St. Louis, MO, USA) containing 10% human serum, 100 U/ml penicillin, and 100 μg/ml streptomycin (Sigma–Aldrich) was added to the same flasks (Corning Inc., Corning, NY, USA) containing collagenase solution and placed at 37 °C in an incubator at 95% humidity and 5% CO2. The medium was renewed after three days. Cells were used at passage 3 for all further experiments.
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