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Dulbecco s modified eagle s culture medium

Manufactured by Merck Group
Sourced in United States

Dulbecco's modified Eagle's culture medium is a widely used cell culture medium formulation. It is designed to support the growth and maintenance of a variety of cell types in vitro. The medium provides essential nutrients, growth factors, and other components necessary for cell proliferation and survival.

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4 protocols using dulbecco s modified eagle s culture medium

1

Preparation of Graphene Oxide Hydrocolloids

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GO colloid (GO) (purity 99.99%) was purchased from Nanopoz (Poznan, Poland) and rGO was purchased from Graphene Laboratories Inc. (Ronkonkoma, NY, USA) and dispersed in ultrapure water to prepare a 1.0 mg/mL solution.
After 30 min of sonification, the hydrocolloids of GO and rGO were diluted to different concentrations with 1× Dulbecco’s modified Eagle’s culture medium (Sigma-Aldrich, St Louis, MO, USA) immediately before exposure to cells.
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2

Culturing SW620 Colorectal Cancer Cells

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Human SW620 colorectal adenocarcinoma cells derived from lymph node metastasis were obtained from American Type Culture Collection and maintained in Dulbecco's Modified Eagle's culture medium (Sigma-Aldrich, Dorset, UK) supplemented with 2 mM L-glutamine, 100 U ml−1 penicillin, 0.2 mg ml−1 streptomycin and 10% (v/v) fetal bovine serum in a humidified atmosphere with 5% CO2 at 37 °C.
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3

Synthesis and Characterization of Platinum Nanoparticles

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The colloid of platinum nanoparticles was purchased from Nano-koloid (Warsaw, Poland). This material is produced by a patented electric non-explosive method (Polish patent 380649) from high-purity metal (99.9999%) and high-purity demineralized Milli-Q water. Graphene oxide powder (GO) (purity 99.99%) was purchased from CEZEMAT (Warsaw, Poland) and dispersed in ultrapure water to prepare a 1.0 mg/mL solution.
After 30 minutes of sonification, the hydrocolloids of GO-NP-Pt, NP-Pt, and GO were diluted to different concentrations with 1× Dulbecco’s modified Eagle’s culture medium (Sigma-Aldrich, St. Louis, MO, USA) immediately prior to exposure to cells.
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4

Preparation of CaP_Si Powder Suspensions

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Following the sterilization under ultraviolet light (15 min), CaP_Si powders were soaked in high-glucose Dulbecco’s modified Eagle’s culture medium (DMEM, Sigma-Aldrich), supplemented with 10% fetal bovine serum (FBS, Capricorn Scientific, Ebsdorfergrund, Germany) and 1% penicillin–streptomycin (Capricorn Scientific), at a concentration of 10 mg/mL. After incubation at 4 °C for 24 h, CaP_Si powders suspensions were centrifuged at 300× g for 5 min in order to spin down the powders.
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