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Language: English
Published by Birkhauser Verlag AG, 2004
ISBN 10: 3764322241 ISBN 13: 9783764322243
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Condition: New. There is an acceleration in prion disease research because of the spread of mad cow disease. This book covers in vitro, cellular, and animal models adapted for the study of TSEs. It includes bio-saftey procedures. Editor(s): Lehmann, Sylvain; Grassi, Jacques. Series: Methods and Tools in Biosciences and Medicine. Num Pages: 221 pages, 8 black & white tables, biography. BIC Classification: MJN. Category: (P) Professional & Vocational. Dimension: 254 x 178 x 12. Weight in Grams: 448. . 2004. Softcover reprint of the original 1st ed. 2004. Paperback. . . . .
Language: English
Published by Birkhauser Verlag AG, 2004
ISBN 10: 3764322241 ISBN 13: 9783764322243
Seller: Kennys Bookstore, Olney, MD, U.S.A.
Condition: New. There is an acceleration in prion disease research because of the spread of mad cow disease. This book covers in vitro, cellular, and animal models adapted for the study of TSEs. It includes bio-saftey procedures. Editor(s): Lehmann, Sylvain; Grassi, Jacques. Series: Methods and Tools in Biosciences and Medicine. Num Pages: 221 pages, 8 black & white tables, biography. BIC Classification: MJN. Category: (P) Professional & Vocational. Dimension: 254 x 178 x 12. Weight in Grams: 448. . 2004. Softcover reprint of the original 1st ed. 2004. Paperback. . . . . Books ship from the US and Ireland.
Language: English
Published by Birkhäuser Basel, Birkhäuser Basel, 2004
ISBN 10: 3764322241 ISBN 13: 9783764322243
Seller: AHA-BUCH GmbH, Einbeck, Germany
Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - Prion diseases, also known as Transmissible Spongiform Encephalopathies (TSEs), exist in both humans (Creutzfeldt-Jakob disease (CJD)) and animals (scrapie, bovine spongiform encephalopathy (BSE), chronic wasting disease) and have the unique property of being infectious, sporadic or genetic in origin.Although the precise nature of the infectious agent responsible for TSEs is not definitely identified, it is now clearly demonstrated that a protein named PrP (for Prion Protein) plays a critical role in the transmission and pathogenesis of TSEs.This book provides the general description as well as the details of the techniques currently used for the study of prion diseases. Taking into account the pivotal role played by PrP it is not surprising that many Chapters of this book deal with the purification, the detection and the characterization of the different forms of this protein. In addition, in vitro, cellular and animal models specifically adapted to the study of TSEs, as well as bio-safety procedures are described. Each Chapter is written by scientists involved for many years in their respective domain of prion biology who give the best of their knowledge in this technical document. This volume is a very useful tool for any laboratory which recently decided to contribute to the study of TSEs as well as for teams already engaged in this field for many years but interested in extending their technical capacity toward new methods.Features:Purification of PrPC and the Pathological Isoform of Prion Protein (PrPsc or PrP-res)Animal Models of TSEsCell Culture Models of TSEsPrPsc ImmunohistochemistryWestern Immunoblotting TechniquesAntibody Production and ELISATSE Strain Typing in MiceBiosafety and Decontamination ProceduresCell-free Conversion of Prion ProteinsCytotoxicity of PrP PeptidesCyclic Amplification of Prion Protein MisfoldingOf interest to:Researchers and clinicians in the fields of cell biology, biomedicine, neuroscience/neuropathology, veterinary medicine and biochemistry.
Taschenbuch. Condition: Neu. Techniques in Prion Research | Jacques Grassi (u. a.) | Taschenbuch | x | Englisch | 2004 | Birkhäuser Basel | EAN 9783764322243 | Verantwortliche Person für die EU: Springer Basel AG in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
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Condition: New. pp. x + 219 2004th edition.
Buch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - Prion diseases, also known as Transmissible Spongiform Encephalopathies (TSEs), exist in both humans (Creutzfeldt-Jakob disease (CJD)) and animals (scrapie, bovine spongiform encephalopathy (BSE), chronic wasting disease) and have the unique property of being infectious, sporadic or genetic in origin.Although the precise nature of the infectious agent responsible for TSEs is not definitely identified, it is now clearly demonstrated that a protein named PrP (for Prion Protein) plays a critical role in the transmission and pathogenesis of TSEs.This book provides the general description as well as the details of the techniques currently used for the study of prion diseases. Taking into account the pivotal role played by PrP it is not surprising that many Chapters of this book deal with the purification, the detection and the characterization of the different forms of this protein. In addition, in vitro, cellular and animal models specifically adapted to the study of TSEs, as well as bio-safety procedures are described. Each Chapter is written by scientists involved for many years in their respective domain of prion biology who give the best of their knowledge in this technical document. This volume is a very useful tool for any laboratory which recently decided to contribute to the study of TSEs as well as for teams already engaged in this field for many years but interested in extending their technical capacity toward new methods.Features:Purification of PrPC and the Pathological Isoform of Prion Protein (PrPsc or PrP-res)Animal Models of TSEsCell Culture Models of TSEsPrPsc ImmunohistochemistryWestern Immunoblotting TechniquesAntibody Production and ELISATSE Strain Typing in MiceBiosafety and Decontamination ProceduresCell-free Conversion of Prion ProteinsCytotoxicity of PrP PeptidesCyclic Amplification of Prion Protein MisfoldingOf interest to:Researchers and clinicians in the fields of cell biology, biomedicine, neuroscience/neuropathology, veterinary medicine and biochemistry.
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Seller: Mispah books, Redhill, SURRE, United Kingdom
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Hardcover. Condition: Brand New. 1st edition. 219 pages. German language. 9.50x6.75x0.50 inches. In Stock.
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Published by Roma, Academia Nazionale dei Lincei, 1974, grand in-8 broché, 179 pp., 1974
Seller: LE SERPENT QUI PENSE, PRECHAC, France
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Publication Date: 1969
Seller: Desván del Libro / Desvan del Libro, SL, MADRID, M, Spain
TAPA DURA. CASTELLANO ACERVO: ANTOLOGIA DE NOVELAS DE ANTICIPACION-IX SIN SOBRECUBIERTA-MARCAS DE USO EN LAS CUBIERTAS-RESTO BUEN ESTADO.
Language: French
Published by Palazzo Grassi, Venise, 2008
ISBN 10: 8861304907 ISBN 13: 9788861304901
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Condition: Bon. Dust Jacket Condition: Bon. 694 pages : illustrations, cartes ; 24,8 x 29,2 x 4,6 cm || Texte français.
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Language: English
Published by Springer, Basel, Birkhäuser Basel, Birkhäuser Nov 2004, 2004
ISBN 10: 3764322241 ISBN 13: 9783764322243
Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Prion diseases, also known as Transmissible Spongiform Encephalopathies (TSEs), exist in both humans (Creutzfeldt-Jakob disease (CJD)) and animals (scrapie, bovine spongiform encephalopathy (BSE), chronic wasting disease) and have the unique property of being infectious, sporadic or genetic in origin.Although the precise nature of the infectious agent responsible for TSEs is not definitely identified, it is now clearly demonstrated that a protein named PrP (for Prion Protein) plays a critical role in the transmission and pathogenesis of TSEs.This book provides the general description as well as the details of the techniques currently used for the study of prion diseases. Taking into account the pivotal role played by PrP it is not surprising that many Chapters of this book deal with the purification, the detection and the characterization of the different forms of this protein. In addition, in vitro, cellular and animal models specifically adapted to the study of TSEs, as well as bio-safety procedures are described. Each Chapter is written by scientists involved for many years in their respective domain of prion biology who give the best of their knowledge in this technical document. This volume is a very useful tool for any laboratory which recently decided to contribute to the study of TSEs as well as for teams already engaged in this field for many years but interested in extending their technical capacity toward new methods.Features:Purification of PrPC and the Pathological Isoform of Prion Protein (PrPsc or PrP-res)Animal Models of TSEsCell Culture Models of TSEsPrPsc ImmunohistochemistryWestern Immunoblotting TechniquesAntibody Production and ELISATSE Strain Typing in MiceBiosafety and Decontamination ProceduresCell-free Conversion of Prion ProteinsCytotoxicity of PrP PeptidesCyclic Amplification of Prion Protein MisfoldingOf interest to:Researchers and clinicians in the fields of cell biology, biomedicine, neuroscience/neuropathology, veterinary medicine and biochemistry. 221 pp. Englisch.
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Kartoniert / Broschiert. Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Topical methodology volumeDetailed description of techniques currently used for the study of prion diseasesWritten by experienced scientists involved in prion research since many years-There is an acceleration in prion disease re.