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 139
Medlin and coworkers ' describe other rDNA primers that amplify the entire 18 $
gene from lower eukaryotes ; these primers will be more useful than NS1 and
NS2 for phylogenetic studies of these organisms . Primers for Mitochondrial DNA
...
Medlin and coworkers ' describe other rDNA primers that amplify the entire 18 $
gene from lower eukaryotes ; these primers will be more useful than NS1 and
NS2 for phylogenetic studies of these organisms . Primers for Mitochondrial DNA
...
Page 146
in behavioral and ecological studies where disturbance of the subjects must be
minimized . The ability to amplify sequences from forensic samples such as
single hairs ? offers new opportunities for behavioral scientists and conservation
...
in behavioral and ecological studies where disturbance of the subjects must be
minimized . The ability to amplify sequences from forensic samples such as
single hairs ? offers new opportunities for behavioral scientists and conservation
...
Page 154
This type of detection required family studies to determine in each parent the
allele type of the polymorphism that is tracking with the normal B - globin gene
and the allele type that is tracking with the sickle B - globin gene . Family studies
may ...
This type of detection required family studies to determine in each parent the
allele type of the polymorphism that is tracking with the normal B - globin gene
and the allele type that is tracking with the sickle B - globin gene . Family studies
may ...
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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