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Full Description
Advances in bioscience research usually arise as a result of the continu- ing refinement of existing technologies. However, there are a number of occa- sions v^rhere newly developed methodologies have a profound effect on nearly all areas of research. Frequently these are techniques that are elegantly simple in concept and require minimal technical manipulation. Two of these revolu- tionary techniques are the focus ofPCR Sequencing Protocols. The first such technique is enzymatic chain termination sequencing developed by Sanger and his co-workers in Cambridge and reported in 1977. This essentially brought the possibility of deriving nucleotide sequence information in a very short time scale and has been widely accepted in many laboratories as a routine molecular biological research tool. Furthermore, it has not only led to the sequencing of many genes and gene fragments, but has also allowed the tech- nical means of sequencing the human genome. The second technique that has found widespread acceptance in basic applied research and many routine applications is the polymerase chain reac- tion. This technique, first reported in 1985 by MuUis and his colleagues, pro- vides the means to amplify nucleic acid sequence, which immediately proved invaluable in nearly all fields of biological laboratory research. Here, as with enzymatic DNA sequencing, is a very simple concept that relies on minimal information to prepare short oligonucleotide primers that direct the synthesis of a specified fi-agment o f DNA in the presence of a thermostable DNA polymerase.
Contents
Preparation and Analysis of DNA Sequencing GelsPurification of PCR Products from Agarose Gels for Direct SequencingEnzymatic Fluorescence and Biotin Labeling of Primers for PCR SequencingDirect Sequencing of Double-Stranded PCR Products with the Sequencase Kit and [a-35S] dATPDirect Sequencing by Thermal Asymmetric PCRRapid Sequencing of cDNA Clones: Direct Sequencing Using Sequential Linear/Asymmetric PCRDirect Sequencing of PCR Products Using Chemiluminescent DetectionDirect DNA Sequencing of PCR Products Using Magnetic BeadsAffinity Capture and Solid-Phase Sequencing Biotinylated PCR ProductsAnalysis of Nucleotide Sequence Variations by Solid-Phase Minisequencing.Nonradioactive PCR Sequencing Using DigoxygeninSilver SequencingTM: Nonradioactive Cycle Sequencing of dsDNADirect Sequencing of PCR Products with DNA-Binding ProteinsPCR Sequencing with the Aid of DetergentsDirect Sequencing with Highly Degenerate and Inosine-Containing PrimersDetermination of Unknown Genomic Sequences Without CloningDNA Sequencing by the Chemical MethodDirect PCR Sequencing with Denaturants (Formamide)Efficient PCR Production of Single-Stranded DNA Sequencing TemplatesPreparation and Direct Automated Cycle Sequencing of PCR ProductsSolid-Phase Automated Sequencing of PCR-Amplified Genomic DNACloning PCR Products for Sequencing in M13 VectorsSequencing PCR Products Cloned into M13 VectorsGenome Amplification with Transcript Sequencing (GAWTS)DNA Rescue by Vectorette MethodSequencing (dAidT) of Cloned Mixed PCR Products from Microbial PopulationsIndex
