Assessment of γH2AX expression for studying DNA double-strand break formation is often performed by manual counting of foci using immunofluorescence microscopy, an approach that is laborious and subject to significant foci selection bias. Here we present a novel high-throughput method for detecting DNA double-strand breaks using automated image cytometry assessment of cell average γH2AX immunofluorescence. Our technique provides an expedient, high-throughput, objective, and cost-effective method for γH2AX analysis.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331074 | PMC |
http://dx.doi.org/10.2144/000114248 | DOI Listing |
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