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
... 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 % NuSieve agarose gel , dried down , and ...
... 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 % NuSieve agarose gel , dried down , and ...
Page 131
... 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 ...
... 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 ...
Page 161
... addition to the two smaller fragments derived from cleavage of the polymorphic Xbal site ( Figure 4 ) . Females who are +/- for the polymorphic site cannot be differentiated from those who are + / + . This complication does not exist ...
... addition to the two smaller fragments derived from cleavage of the polymorphic Xbal site ( Figure 4 ) . Females who are +/- for the polymorphic site cannot be differentiated from those who are + / + . This complication does not exist ...
Contents
PART ONE BASIC METHODOLOGY | 1 |
The Design and Optimization of the PCR | 7 |
Taq DNA Polymerase | 17 |
Copyright | |
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Other editions - View all
PCR Technology: Principles and Applications for DNA Amplification Henry Erlich No preview available - 1989 |
Common terms and phrases
Acad Acids Res aliquot alleles amplification amplification products amplified DNA annealing Arnheim assay automated B-globin gene base cDNA cells Cetus chromosome clones concentration containing cycles deletion denaturation denaturing gradient gel detection DGGE diagnosis digestion direct sequencing disease DNA fragments DNA sequence dNTP dot-blot dystrophin Erlich exon Faloona Figure flanking GC-clamp gel electrophoresis genetic genomic genomic DNA heteroduplex Higuchi HPRT human hybridization identified incubation individual inverse PCR lane loci locus markers melting method mismatch molecular molecules mRNA Mullis Natl Nucl nucleotide oligonucleotide primers oligonucleotide probes PCR amplification PCR analysis PCR primers PCR product PCR reaction pmol polymerase chain reaction polymorphic primers Proc procedure protein Protocol ras gene recombination region restriction enzyme reverse transcriptase Saiki Scharf single sperm Sninsky Southern blot specific sperm ssDNA strand synthesis Taq DNA polymerase Taq polymerase target sequence temperature template Tris.HCl tube tumors