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 55
P CTP ( 10 uCi / ul , 1000 mCi / mmol ) , in addition to the cold nucleotides
already present . After amplification the unincorporated nucleotides were
removed using a Centricon 10 ( Amicon ) , and 1 % of the probe electrophoresed
on a 4 ...
P CTP ( 10 uCi / ul , 1000 mCi / mmol ) , in addition to the cold nucleotides
already present . After amplification the unincorporated nucleotides were
removed using a Centricon 10 ( Amicon ) , and 1 % of the probe electrophoresed
on a 4 ...
Page 131
In addition to the sequence information that would be required for primer
synthesis , RFLPs have usually not been analyzed extensively enough so as to
reveal the nature of the nucleotide substitution . In some cases , the PCR product
can be ...
In addition to the sequence information that would be required for primer
synthesis , RFLPs have usually not been analyzed extensively enough so as to
reveal the nature of the nucleotide substitution . In some cases , the PCR product
can be ...
Page 161
2 In addition , our laboratory is able to carry out B - globin cluster haplotyping by
PCR analysis of five restriction site polymorphisms ( unpublished data ) . If we
ever encounter difficulty in direct detection of sickle cell anemia or B -
thalassemia ...
2 In addition , our laboratory is able to carry out B - globin cluster haplotyping by
PCR analysis of five restriction site polymorphisms ( unpublished data ) . If we
ever encounter difficulty in direct detection of sickle cell anemia or B -
thalassemia ...
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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