Proceedings of the Second International PCR Symposium on Usage of PCR and Alternative Amplification Methods in Infectious and Genetic Diseases held in Berlin, Germany, February 26-27, 1993

Springer Book Archives

General Aspects of PCR: The Polymerase Chain Reaction and Fixed Tissues; J.J. O'Leary. Impact of PCR on the Pathologist's World; D. Myerson. Sensitive and Rapid Detection and Quantification of Nucleic Acids; L. Cross, et al. Alternative DNA-amplification Methods: Ligase-mediated Detection Methods; M. Wiedmann, et al. Qualitative and Quantitative Detection of Nucleic Acids of Infectious Agents by NASBA; B. van Gemen, et al. Application of NASBA to the Detection of Listeria Monocytogenes; J. Kleiber, et al. PCR and Virological Problems: Confirmation of Hepatitis C Virus Carrier State by Polymerase Chain Reaction in Cases with Nondiagnostic Serologies; C.H. Wang, B. Flehmig. Confirmation of Hepatitis C Virus Positive Seras by Polymerase Chain Reaction; G. Lucotte, et al. PCR in the Field of Bacterial and Fungal Problems: Identification of Toxoplasma-DNA by Polymerase Chain Reaction in Peripheral Blood Leukocytes of Patients with Suspected Toxoplasmosis; G. Koch, et al. Detection of Mycobacterium Tuberculosis in Clinical Samples by Polymerase Chain Reaction; G.M. Lucchini, M. Altwegg. 17 additional articles. Index.

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.