A proven collection of readily reproducible techniques for studying amyloid proteins and their involvement in the etiology, pathogenesis, diagnosis, and therapy of amyloid diseases. The contributors provide methods for the preparation of amyloid and its precursors (oligomers and protofibrils), in v
Amyloid Proteins: Methods and Protocols
β Scribed by Gal Bitan, David B. Teplow (auth.), Einar M. Sigurdsson (eds.)
- Publisher
- Humana Press
- Year
- 2005
- Tongue
- English
- Leaves
- 407
- Series
- Methods in Molecular Biology 299
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Subjects
Biochemistry, general
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Amyloid diseases are characterized by the deposition of insoluble fibrous amyloid proteins. The word βamyloidβ indicates a starch-like compound, and though a misnomer, continues to be the accepted term for this group of protein conformational disorders. The second editionΒ of Amyloid Proteins expand
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<p>This detailed volume focuses on methods for the characterization of aggregation processes that lead to the formation of amyloid fibrils and amyloid oligomers which feature in the etiology of a variety of human disorders collectively known as amyloidoses. The scope of the collection includes techn
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