PCR Technology: Principles and Applications for DNA AmplificationThis is an introduction to the methods and applications of polymerase chain reaction (PCR) technology, a technology developed by Erlich's group at Cetus and Cetus, and is expected to be used in all biology laboratories worldwide within the next few years. |
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Page 36
... buffer w / nonionic detergents and Proteinase K " to give about 6x10 cells per ml . Transfer to 1.5 - ml Eppendorf ... buffer , and 2x in triphosphate , primers , and enzyme . Make up any deficiency in volume with water . With RBC ...
... buffer w / nonionic detergents and Proteinase K " to give about 6x10 cells per ml . Transfer to 1.5 - ml Eppendorf ... buffer , and 2x in triphosphate , primers , and enzyme . Make up any deficiency in volume with water . With RBC ...
Page 58
... buffer ( 50 mM KCl , 50 mM Tris.HCl , pH 8.0 , 5 mM MgCl2 , 10 mM dithiothreitol ) . Heat the reaction on ice for 10 min and then transfer the tube to ice . Transfer 2.2 μl of the mixture to each of four tubes with deoxy - dideoxy mixes ...
... buffer ( 50 mM KCl , 50 mM Tris.HCl , pH 8.0 , 5 mM MgCl2 , 10 mM dithiothreitol ) . Heat the reaction on ice for 10 min and then transfer the tube to ice . Transfer 2.2 μl of the mixture to each of four tubes with deoxy - dideoxy mixes ...
Page 166
... buffer : Wash buffer : 1 % Ficoll 1 % PVP ( polyvinyl pyrrolidone ) 1 % BSA 5 X SSPE 0.5 % SDS 5 X Denhardt's 2 X SSPE 0.1 % SDS For end - labeling : Allele - specific oligonucleotide ( ASO ) Kinase buffer recommended by T4 kinase ...
... buffer : Wash buffer : 1 % Ficoll 1 % PVP ( polyvinyl pyrrolidone ) 1 % BSA 5 X SSPE 0.5 % SDS 5 X Denhardt's 2 X SSPE 0.1 % SDS For end - labeling : Allele - specific oligonucleotide ( ASO ) Kinase buffer recommended by T4 kinase ...
Contents
PART ONE BASIC METHODOLOGY | 1 |
The Design and Optimization of the PCR | 7 |
PCR Amplification of Specific Sequences from | 9 |
Copyright | |
17 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 Res agarose alleles amplification amplification products amplified DNA analysis annealing assay automated cDNA cells Cetus chromosome cloned concentration containing cycles deletion denaturant denaturing gradient gel detection DGGE diagnosis direct sequencing disease DNA fragments DNA sequence dNTP dot-blot dystrophin Erlich exon Faloona Figure flanking GC-clamp Gelfand genetic genomic genomic DNA heteroduplexes Higuchi HPRT human hybridization incubation individual inverse PCR lane Lerman loci locus markers melting behavior melting domain method misincorporation mismatch molecular molecules mRNA Mullis mutations Natl Nucl nucleotide oligonucleotide primers PCR amplification PCR buffer PCR fragments PCR primers PCR product PCR reaction pmol polymerase chain reaction polymorphism primers Proc procedure protein Proteinase Proteinase K Protocol recombination region restriction enzyme reverse transcriptase Saiki Scharf sequencing reactions single-stranded specific ssDNA strands synthesis Taq DNA polymerase Taq polymerase target DNA target sequence temperature template Tris.HCl tube