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Abstract

<jats:p>&lt;p&gt;Figure S19. SETD2 WT and SETD2-deficient A498 cells were treated with ethidium bromide to deplete mitochondrial DNA (mtDNA). Cells were subsequently treated with DMSO or 100nM A-1331852 for 72 hours, and total DNA was isolated. mtDNA levels were quantified by qPCR. GAPDH was used as an endogenous reference.&lt;/p&gt;</jats:p>

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cells treated mtdna pfigure setd2

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