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In den WarenkorbHardcover. Zustand: Très bon. Edition 1997. Tome 74. Ammareal reverse jusqu'à 15% du prix net de cet article à des organisations caritatives. ENGLISH DESCRIPTION Book Condition: Used, Very good. Edition 1997. Volume 74. Ammareal gives back up to 15% of this item's net price to charity organizations.
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In den WarenkorbHardcover. Zustand: Très bon. Edition 1997. Tome 74. Ammareal reverse jusqu'à 15% du prix net de cet article à des organisations caritatives. ENGLISH DESCRIPTION Book Condition: Used, Very good. Edition 1997. Volume 74. Ammareal gives back up to 15% of this item's net price to charity organizations.
Sprache: Englisch
Verlag: Totowa, New Jersey: Humana Press (Methods in Molecular Biology) 1st edn, 1997
ISBN 10: 0896033899 ISBN 13: 9780896033894
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Zustand: New. This text presents techniques for the determination of ribozyme structure; for delivery systems for ribozymes; and for their applications. Each is presented with background support in the form of troubleshooting advice, as well as hints and tips geared to the completion of an experiment. Editor(s): Turner, Philip C. Series: Methods in Molecular Biology. Num Pages: 492 pages, 54 black & white illustrations, biography. BIC Classification: PDN; PSD; PSF. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 28. Weight in Grams: 1960. . 1997. Hardback. . . . . Books ship from the US and Ireland.
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Buch. Zustand: Neu. Neuware - The purpose of Ribozyme Protocols is to provide a helpful compilation of protocols that will be of use-^not only to those with some experience of ribozymes-^but also to those wishing to use ribozymes for the first time. Although it is usually impossible to cover every aspect of a scientific field, I believe this book approaches that ideal and should help all readers perform meaningful experiments using ribozymes. To design ribozymes, one must consider whether the target site will be accessible; this task can be facilitated by using computer programs that pre dict the folding of the target RNA. Such programs are detailed in Chapters 2 and 3. If the chosen target is an RNA virus that can mutate rapidly, it makes sense to consider those parts of the genome that are least likely to change during viral replication. An example of how this can be done is described in Chapter 4. Although computer analysis may be a useful starting point to select tar get sites, there seems, at the moment, to be no guarantee that any particular chosen site will be efficiently cleaved. Some workers have deliberately bypassed this problem by using libraries of ribozyme sequences and by select ing those that actually hybridize to and/or cleave the target; these methods are described in Chapters 5 and 6.