Condition: New. pp. 152 1st Edition.
Seller: Bernhard Kiewel Rare Books, Grünberg, Germany
25 cm XIX, 271 Seiten. Mit 95 Figures. OPb. Ordnungsgemäß aus einer Universitäts-Bibliothek ausgesondert (Stempel, Signatur). Guter Zustand. Sprache: Englisch Gewicht in Gramm: 923.
Language: English
Published by Springer-Verlag Telos, 1992
ISBN 10: 0387554408 ISBN 13: 9780387554402
Seller: Romtrade Corp., STERLING HEIGHTS, MI, U.S.A.
Condition: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
Seller: Majestic Books, Hounslow, United Kingdom
Condition: New. pp. 152.
Seller: Biblios, Frankfurt am main, HESSE, Germany
Condition: New. pp. 152.
Language: English
Published by Springer-Verlag Inc, Berlin, 1991
ISBN 10: 3540529349 ISBN 13: 9783540529347
First Edition
Condition: Very Good. First Edition. VG : in very good condition without dust jacket as issued. 230mm x 150mm (9" x 6"). xi, 258pp. Illustrated laminated card cover.
Condition: New. pp. 262.
Condition: New. pp. 262 27 Illus.
Condition: New. pp. xi + 258 Index.
Condition: New. pp. xi + 258 Illus.
Condition: New. pp. 262.
Condition: Used. pp. 370 1st Edition.
Seller: Ria Christie Collections, Uxbridge, United Kingdom
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Paperback. Condition: Very Good. No Jacket. May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less 0.96.
Seller: Revaluation Books, Exeter, United Kingdom
Paperback. Condition: Brand New. 151 pages. 10.00x7.01x0.36 inches. In Stock.
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Add to basketHardcover. Condition: Très bon. Ancien livre de bibliothèque avec équipements. Edition 1994. Ammareal reverse jusqu'à 15% du prix net de cet article à des organisations caritatives. ENGLISH DESCRIPTION Book Condition: Used, Very good. Former library book. Edition 1994. Ammareal gives back up to 15% of this item's net price to charity organizations.
Paperback. Condition: Brand New. 1994 edition. 260 pages. 9.61x6.14x0.60 inches. In Stock.
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Language: English
Published by Springer US, Chapman And Hall/CRC, 2012
ISBN 10: 1461374553 ISBN 13: 9781461374558
Seller: AHA-BUCH GmbH, Einbeck, Germany
Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - In the ten years since the first publication on PCR (Saiki et al. , 1985), this in vitro method of nucleic acid replication and modification has grown to rival in popularity traditional microbiological, genetical und technical procedures for cloning, sequencing, gene detecting and related procedures. To date the PCR literature has emphasized six main areas of application: genetic mapping, detection of mutations, genetic polymorphism, transcriptional splicing and regulation, molecular virology and quantitative procedures. The overwhelming focus of quantification of DNA or RNA by PCR has been on human microbiology and oncological problems. The exquisite sensitivity of PCR gives this method the ability to detect extremely rare DNAs, mRNAs, mRNAs in small numbers of cells or in small amounts of tissue, and mRNAs expressed in mixed-cell populations. However, the exact and accurate quantification of specific nucleic acids in biological samples is in spite of numerous publications in that field still a general problem: during the peR process, an unknown initial number of target sequences are used as a template from which a large quantity of specific product can be obtained. Although the amount of product formed is easy to determine, it is difficult to deduce the initial copy number of the target molecule because the efficiency of the peR is largely unknown.
Taschenbuch. Condition: Neu. Druck auf Anfrage Neuware - Printed after ordering - The polymerase chain reaction (PCR) - an in Vitro techniques for producing large amounts of a specific DNA fragment - has rapidly become established as one of the most important, impressive and fascinating methods of molecular biology as well as clinical diagnostics. In the seven years since'the technique was published, it has had a major impact on medical research. However, as there are still problems in instruments, standardized protocols for diagnostic applications and unsolved difficulties to avoid cross-contaminations on the one hand and on the other hand the even present question of how to interpret the biological value of a PCR result, most clinicians prefer to further wait until these topics are clarified. It is the aim of this book to give the reader lab-proven protocols from experienced scientists as well as a general introduction to alternative DNA-amplification procedures and their possible usage such as the NASBA or LCR. This book is divided into four major parts to provide a theoretical (first and second section) and a practical framework for a better understanding of the new technology. In the first part we provide an up-to-date summary of basic problems in this rapidly evolving field. We demonstrate, for example how to use fixed tissue materials and how to quantify PCR products as well as how to prepare nucleic acids in a safe, convenient and proper way, or even how to sequence directly PCR products for the analysis of the DNA structure.