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Poly hema coated

Manufactured by Corning

Poly-HEMA-coated is a laboratory equipment product. It serves as a coating material. The core function of Poly-HEMA-coated is to provide a surface modification for various laboratory applications.

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2 protocols using poly hema coated

1

Antiproliferative Screening Assay in 2D and 3D

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For assays in 2D culture, cells were seeded at predetermined optimal densities in 96-flat-well plates (Corning). For assays in 3D cultures, 1000 cells per well were seeded in Poly-HEMA-coated (0.6 mg per well) 96 round-well plates (Corning). In addition, cells were pelleted at 300 g for 3 min to facilitate more homogenous spheroid growth. Twenty-four hours post seed, compounds for treatments were added and incubated for another 96 h. XTT assay reagent (neoFroxx) was added, and after development, absorbance was read at 463 vs. 670 nm on a TECAN Infinite M1000 Pro reader. Data shown are expressed as percentage of metabolic activity compared to untreated or vehicle-treated cells, corrected by subtraction of blank values. Titration curves were fitted with a “log(inhibitor) vs. response—variable slope (four parameters)” fit (GraphPad Prism). Data were weighted by 1/Y2 and the Hill slopes were constrained to >“−3”. Antiproliferative effects were compared by calculating the area under the curve with a 95% confidence interval. Nonoverlapping areas were considered different. Single concentration points were compared by the two-sided Student’s t test or two-sided ANOVA where applicable and corrected for multiple testing where due; see individual figure captions for detailed description of applied statistical tests.
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2

Evaluating Cell Responses to PF-271

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Cells were plated in 6-well plates under non-adherent (25 × 104 cells, poly-HEMA coated, Corning) or adherent (5 × 104 cells, tissue culture-treated plastic, Corning) conditions. PF-271, dissolved in dimethyl sulfoxide (DMSO), was added at the indicated concentration. After three days, all cells were collected by limited trypsin treatment, a single cell suspension was prepared, and the viable total cell number determined by ViCell XR (Beckman). All experimental points were performed in triplicate and repeated at least two times.
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