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In vivo imaging of DNA double-strand break induced telomere mobility during alternative lengthening of telomeres
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文摘
mCherry-ER-DD-TRF1-FokI is used to visualize DSB-induced telomere mobility. DSB generation and tracking are performed using a single protein. Transfection and imaging can be accomplished in as little as 48 h. Telomere mobility can be analyzed quantitatively using a semi-automated workflow.

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