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ELISA Method for Measurement of Amyloid-ß Levels
Abstract
The neuritic plaque in the brain of Alzheimer's disease (AD) patients consists of an amyloid composed primarily of Aß, an approx 4-kDa peptide derived from the amyloid precursor protein. Multiple lines of evidence suggest that Aß plays a key role in the pathogenesis of the disease, and potential treatments that target Aß production and/or Aß accumulation in the brain as ß-amyloid are being aggressively pursued. Methods to quantitate the Aß peptide are, therefore, invaluable to most studies aimed at a better understanding of the molecular etiology of the disease and in assessing potential therapeutics. Although other techniques have been used to measure Aß in the brains of AD patients and ß-amyloid-depositing transgenic mice, the enzyme-linked immunosorbent assay (ELISA) is one of the most commonly used, reliable, and sensitive methods for quantitating the Aß peptide. Here we describe methods for the recovery of both soluble and deposited Aß from brain tissue and the subsequent quantitation of the peptide by sandwich ELISA.
Affiliation(s): (2) Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY
(3) Departments of Psychiatry and Cell Biology, New York University School of Medicine, New York, NY
(4) Department of Psychiatry, New York University School of Medicine, New York, NY
Series: Methods in Molecular Biology  |  Volume: 299  |  Pub. Date: Dec-28-2004  |  Page Range: 279-297  |  DOI: 10.1385/1-59259-874-9:279
Subject:  Protein Science
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