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090727 ||| eng |
020 |
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|a 9781592592739
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050 |
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|a QH573-671
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100 |
1 |
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|a Theophilus, Bimal D. M.
|e [editor]
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245 |
0 |
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|a PCR Mutation Detection Protocols
|h Elektronische Ressource
|c edited by Bimal D. M. Theophilus, Ralph Rapley
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250 |
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|a 1st ed. 2002
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260 |
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|a Totowa, NJ
|b Humana Press
|c 2002, 2002
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300 |
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|a X, 214 p
|b online resource
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505 |
0 |
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|a Agarose and Polyacrylamide Gel Electrophoresis -- Internal Labeling of DNA Probes -- End-Labeling of DNA Probes -- Southern Blotting of Agarose Gels by Capillary Transfer -- Restriction Fragment Length Polymorphism -- PCR -- Allele-Specific Oligonucleotide PCR -- Long-Range PCR -- Analysis of Nucleotide Sequence Variations by Solid-Phase Minisequencing -- Cycle Sequencing of PCR Products -- Fluorescent In Situ Hybridization -- The Protein Truncation Test -- Mutation Detection in Factor VIII cDNA from Lymphocytes of Hemophilia A Patients by Solid Phase Fluorescent Chemical Cleavage of Mismatch -- Denaturing Gradient Gel Electrophoresis -- Conformation-Sensitive Gel Electrophoresis -- SSCP/Heteroduplex Analysis -- Cleavase® Fragment Length Polymorphism Analysis for Genotyping and Mutation Detection -- Automated Genotyping Using the DNA MassArray™ Technology -- An Introduction to Bioinformatics
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653 |
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|a Cell Biology
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653 |
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|a Cytology
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700 |
1 |
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|a Rapley, Ralph
|e [editor]
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041 |
0 |
7 |
|a eng
|2 ISO 639-2
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989 |
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|b SPRPROT
|a Springer Protocols Archive 1981-2004
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490 |
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|a Methods in Molecular Biology
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028 |
5 |
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|a 10.1385/1592592732
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856 |
4 |
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|u https://doi.org/10.1385/1592592732?nosfx=y
|x Verlag
|3 Volltext
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|a 571.6
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|a Application of DNA technology to the identification of disease-causing mutations has become widespread in recent years. PCR Mutation Detection Protocols, provides biological and clinical investigators with a comprehensive collection of new, recent, and updated PCR-based screening methods suitable for detecting the presence of both known and novel mutations. The methods cover point mutations (e.g., ASO-PCR, SSCP, DGGE, chemical cleavage), deletions (multiplex PCR, FISH, blotting), non-sense mutations (PTT), and more. The new and exciting techniques of DNA array analysis, along with such recently developed experimental methods as conformation-sensitive gel electrophoresis, are also included. Additional coverage is given to the direct use of DNA sequencing as a detection method in its own right and to the characterization of mutations previously located by other screening techniques. Each chapter explains the basic theory behind the technique and provides valuable notes essential for its successful execution. Comprehensive and highly practical, PCR Mutation Detection Protocols assures both seasoned and novice investigators access to the highly productive and readily reproducible PCR-based mutation detection methods, techniques that are laying the groundwork for many of today's major scientific and medical advances
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