Abstract
Amyloid-containing tissue, whether from human patients or an animal model of a disease, is typically characterized by various biochemical and immunohistochemical techniques, many of which are described in detail in this volume. In this chapter, we describe a straightforward technique for the homogenization of tissue prior to these analyses. The technique is particularly well suited for performing a large number of different biochemical analyses on a single mouse brain hemisphere. Starting with this homogenate multiple characterizations can be done, including western blot analysis and isolation of membrane-associated proteins, both of which are described here. Additional analyses can readily be performed on the tissue homogenate, including the ELISA quantitation of Aβ in the brain of a transgenic mouse model of β-amyloid deposition. The ELISA technique is described in detail in Chapter 34.
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Acknowledgments
This work has been supported by the Alzheimer’s Association (IIRG-07-60047 to P.M.M.) and the National Institute on Aging (AG017617 to P.M.M., R.A.N.). We thank Dr. Karen Duff (Columbia University) for the transgenic mouse brains used in the sample data.
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Schmidt, S.D., Nixon, R.A., Mathews, P.M. (2012). Tissue Processing Prior to Analysis of Alzheimer’s Disease Associated Proteins and Metabolites, Including Aβ. In: Sigurdsson, E., Calero, M., Gasset, M. (eds) Amyloid Proteins. Methods in Molecular Biology, vol 849. Humana Press. https://doi.org/10.1007/978-1-61779-551-0_33
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DOI: https://doi.org/10.1007/978-1-61779-551-0_33
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