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Methods in DNA Amplification

Book's cover
The cover of “Methods in DNA Amplification” - Open Library.
Methods in DNA Amplification - cover - The Open Library
Book's cover - The Open Library
Methods in DNA Amplification - cover - Google Books
Book's cover - Google Books

"Methods in DNA Amplification" is published by Springer in Nov 07, 2012, the book is classified in Medical genre, it has 260 pages and the language of the book is English.


“Methods in DNA Amplification” Metadata:

  • Title: Methods in DNA Amplification
  • Authors:
  • Language: English
  • Number of Pages: 260
  • Is Family Friendly: Yes - No Mature Content
  • Publisher: Springer
  • Publish Date:
  • Genres: Medical

“Methods in DNA Amplification” Subjects and Themes:

Edition Specifications:

  • Format: paperback

Edition Identifiers:

AI-generated Review of “Methods in DNA Amplification”:


Snippets and Summary:

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.

"Methods in DNA Amplification" Description:

Google Books:

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.

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