PCR Technology: Principles and Applications for DNA AmplificationPolymerase chain reaction (PCR) technology is a revolutionary innovation which enables scientists to rapidly generate large amounts of genetic material from a slight trace which would otherwise be too small to analyze. With applications in both research and diagnostics, PCR is becoming a standard procedure in biotechnology and medical diagnostic laboratories. This book is an introduction and guide to the new technology, covering the basic methodologies and their applications in research and medicine, emphasizing practical aspects. Each chapter is written by pioneers in the field and most include detailed protocols and favorite PCR "recipes". Students and researchers in all areas of biotechnology and molecular biology will find this book the introduction to PCR they've been looking for. |
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Page 149
The detection of infectious disease pathogens and the identification of genetic
variation associated with disease has been ... enough of the target sequence so
that simple , rapid , and robust methods for identifying it could be employed .
The detection of infectious disease pathogens and the identification of genetic
variation associated with disease has been ... enough of the target sequence so
that simple , rapid , and robust methods for identifying it could be employed .
Page 184
21 , 28 , 29 To our knowledge , there are no reports of heterozygous new
mutations identified for the first time by the method , nor of the application of direct
automated DNA sequencing to the problem . Reconstruction experiments are ...
21 , 28 , 29 To our knowledge , there are no reports of heterozygous new
mutations identified for the first time by the method , nor of the application of direct
automated DNA sequencing to the problem . Reconstruction experiments are ...
Page 226
In the years following the initial discovery , many reports appeared identifying
transforming ras genes in a variety of tumor cell ... In one of the procedures , the
transforming mutation is identified by specific hybridization to
oligodeoxynucleotide ...
In the years following the initial discovery , many reports appeared identifying
transforming ras genes in a variety of tumor cell ... In one of the procedures , the
transforming mutation is identified by specific hybridization to
oligodeoxynucleotide ...
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Contents
PART ONE BASIC METHODOLOGY | 1 |
The Design and Optimization of the PCR | 7 |
Taq DNA Polymerase | 17 |
Copyright | |
14 other sections not shown
Other editions - View all
PCR Technology: Principles and Applications for DNA Amplification Henry Erlich No preview available - 1989 |
Common terms and phrases
Acad Acids activity addition alleles allow Alu repeats amount amplification analysis annealing applications approach assay base blood buffer carried cDNA cell changes Chapter clones concentration containing cycles deletion denaturation described detection determined diagnosis digestion direct discussed disease DNA fragments DNA polymerase DNA sequence dNTP domain effect efficient electrophoresis enzyme Erlich example exon extension Figure gene genetic genomic human hybridization identified increase individual initial isolation known lane limited loci locus markers melting method molecular Mullis mutations Nature observed obtained oligonucleotide PCR product performed polymorphic positive possible preparation present primers probes problem Proc procedure Protocol reaction recombination region restriction Saiki samples Science separate shown single specific sperm step strand studies Taq polymerase techniques temperature template tube usually yield