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2 protocols using s8007

1

PrimPol Knockdown Cell Viability Assay

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Cells were seeded in 96-well flat-bottom plates at a density of 2000 cells/well following 24 h of PrimPol siRNA knockdown. Stock solutions of each drug were prepared in sterile water or dimethyl sulfoxide (DMSO) as appropriate and further diluted in growth medium. Cells were allowed to grow for 6 days in drug containing medium (VE-821, SelleckChem S8007, Olaparib, SelleckChem S1060) and cell viability was measured with the CellTiter-Glo Luminescent Cell Viability Assay (Promega G7572) following manufacturer’s instructions. Luminescence was then measured with a PerkinElmer Envision 2103 multilabel plate reader. Viability was calculated as the luminescence signal ratio of treated versus untreated samples. Analysis and statistical test were performed using Microsoft Excel and GraphPad Prism v9.
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2

DNA Damage and Replication Stress Compounds

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Unless stated otherwise the following compounds were used in this manuscript at the indicated final concentrations: ATRi Az-20 (1 μM, 5198, Tocris), ATRi VE-821 (10 μM, S8007, Selleckchem), Camptothecin (50 nM, S1288, Selleckchem), Roscovitine (20 μM, S1153, Selleckchem), Olaparib (10 μl, S1060, Selleckchem), DRB (100 μM, D1916, Sigma), Flavopiridol (1.25 μM, S1230, Selleckchem), AZD5438 (1 μM, S2621, Selleckchem), Hydroxyurea (HU, 2 mM, H8627, Sigma), Doxycycline (1-1000 ng/mL, D9891, Sigma), CDC7i (25 μM, S2742, Selleckchem), Aphidicolin (0.2 μM, A0781, Sigma), Diospyrin D (10 μM, gift of Dr. Pavel Janscak).
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