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    Antibodies for assessing circadian clock proteins in the rodent suprachiasmatic nucleus

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    Authors
    Lesauter, Joseph
    Lambert, Christopher M.
    Robotham, Margaret R.
    Model, Zina
    Silver, Rae
    Weaver, David R.
    UMass Chan Affiliations
    Weaver Lab
    Neurobiology
    Document Type
    Journal Article
    Publication Date
    2012-04-27
    Keywords
    Antibodies
    CLOCK Proteins
    Circadian Clocks
    Suprachiasmatic Nucleus
    Neuroscience and Neurobiology
    
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    Abstract
    Research on the mechanisms underlying circadian rhythmicity and the response of brain and body clocks to environmental and physiological challenges requires assessing levels of circadian clock proteins. Too often, however, it is difficult to acquire antibodies that specifically and reliably label these proteins. Many of these antibodies also lack appropriate validation. The goal of this project was to generate and characterize antibodies against several circadian clock proteins. We examined mice and hamsters at peak and trough times of clock protein expression in the suprachiasmatic nucleus (SCN). In addition, we confirmed specificity by testing the antibodies on mice with targeted disruption of the relevant genes. Our results identify antibodies against PER1, PER2, BMAL1 and CLOCK that are useful for assessing circadian clock proteins in the SCN by immunocytochemistry.
    Source
    LeSauter J, Lambert CM, Robotham MR, Model Z, Silver R, et al. (2012) Antibodies for Assessing Circadian Clock Proteins in the Rodent Suprachiasmatic Nucleus. PLoS ONE 7(4): e35938. doi:10.1371/journal.pone.0035938. Link to article on publisher's site
    DOI
    10.1371/journal.pone.0035938
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/37846
    PubMed ID
    22558277
    Related Resources
    Link to Article in PubMed
    Rights
    Copyright: © 2012 LeSauter et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
    ae974a485f413a2113503eed53cd6c53
    10.1371/journal.pone.0035938
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