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 18
DNA synthesis at higher temperatures in vitro may be limited by the stability of the
primer or priming - strand and the template - strand duplex . Although Taq DNA
polymerase has a very limited ability to synthesize DNA above 90°C , the ...
DNA synthesis at higher temperatures in vitro may be limited by the stability of the
primer or priming - strand and the template - strand duplex . Although Taq DNA
polymerase has a very limited ability to synthesize DNA above 90°C , the ...
Page 25
In general , this type of robotic system is usually simple to set up ; the different
components are available right off the shelf . Also , very little software is needed ,
since the options for control are so limited by the physical system . In summary ,
the ...
In general , this type of robotic system is usually simple to set up ; the different
components are available right off the shelf . Also , very little software is needed ,
since the options for control are so limited by the physical system . In summary ,
the ...
Page 53
This procedure has more limited applicability since it involves additional
enzymatic steps following the amplification reaction , and is restricted to using
reverse transcriptase as sequencing enzyme . the pores attaching a phquencing
has ...
This procedure has more limited applicability since it involves additional
enzymatic steps following the amplification reaction , and is restricted to using
reverse transcriptase as sequencing enzyme . the pores attaching a phquencing
has ...
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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