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2 protocols using hoescht 33342 dye

1

Zinc Oxide Nanoparticle Assays

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Suspensions of n-ZnO (mean particle size 35 nm), reduced glutathione (GSH), bovine serum albumin, phenylmethylsulfonyl fluoride (PMSF), 5,5′-dithio-bis(2-nitrobenzoic acid) (DTNB), nicotinamide adenine dinucleotides (NADH, NAD, NADPH), EDTA, dihydrorhodamine, Hoescht 33342 dye, 2,4-Dinitrophenylhydrazine, tyrosin, hemoglobin, chymotrypsinogen, cytohrome c, myoglobin, ubiquitin, Sephadex G-50, β-mercaptoethanol, ethoxyresorufin, certified reference material ERM-BB422 and Lactobacillus leichmannii D-Lactate dehydrogenase were purchased from Sigma Chem. Co. (St. Louis, USA). All other chemicals were obtained from the Synbias (Kyiv, Ukraine), Bayer (Kyiv, Ukraine) and Balkanpharma-Dupnitsa (Dupnitsa, Bulgaria) commercial suppliers. All reagents were of the analytical grade or higher.
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2

Viability Assessment of hMSCs and MOSJ Cells

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A Live/Dead Cell Imaging Kit (Life Technologies) was employed to assess the viability of both the hMSCs and MOSJ cells on the beads. The assay was carried out according to the manufacturer’s instructions with the exception of the use of Hoescht 33342 dye (Sigma) to visualize dead MOSJ cells as it was not possible to distinguish between the propidium iodide stain and the dsRed2 already expressed by the cells. Live staining was carried out on hMSCs not expressing GFP to allow visualization of the calcein AM dye that indicates live cells.
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