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2: BrdU assay

  • Page ID
    135768
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    Summary

    BrdU is a synthetic nucleoside analog, like the nucleoside thymidine, except the methyl group is replaced with a bromine atom. BrdU can be incorporated into DNA whenever thymidine normally would be, including during DNA replication and repair. Therefore, BrdU is often used to label cells that are undergoing or have recently undergone DNA replication.

    Also known as:

    Bromodeoxyuridine assay, 5-bromo-2′-deoxyuridine assay

    Samples needed

    Live cells are treated with BrdU, which incorporates into DNA being replicated. Subsequent steps depend on how sample will be visualized, for instance by immunofluorescence microscopy or immunohistochemistry.

    Method

    Cells are treated with BrdU for a defined length of time. Any cells undergoing S-phase within the window when BrdU was present will have BrdU incorporated into their DNA. BrdU can be recognized by an anti-BrdU antibody, then visualized by the desired method. In order for BrdU to be accessible for the antibody to bind, the DNA has to be denatured.

    Interpretation

    If a cell is positive for BrdU, it was going through S phase when BrdU was present.

    Special cases

    To assess formation of single-strand DNA (ssDNA)

    Normally, DNA has to be denatured for the BrdU antibody to detect any BrdU incorporated into the DNA. However, if a) BrdU labeling occurs over a long period so that all DNA is labeled and b) BrdU staining is performed under non-denaturing conditions, the only BrdU that will be accessible to the antibody will be in areas where DNA is single-stranded for some other reason (besides denaturing), like replication fork collapse. So, in this case, staining correlates with the amount of ssDNA in a sample.


    Thumbnail

    "BrdU staining (green).jpg" by Jason Snyder is licensed under CC BY 2.0.

    Description: BrdU (green) and arc (red) staining of neurons.

    Author

    Katherine Mattaini, Tufts University


    This page titled 2: BrdU assay is shared under a CC BY-SA 4.0 license and was authored, remixed, and/or curated by Katherine Mattaini.

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