PCR Mutation Detection Protocols

Bimal D.M. Theophilus, Ralph Rapley (Herausgeber)

Buch | Softcover

298 Seiten

2016 | Softcover reprint of the original 2nd ed. 2011
Humana Press Inc. (Verlag)
978-1-4939-5629-6 (ISBN)

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Since the publication of the popular first edition, the explosion of DNA sequence information, the access to bioinformatics and mutation databases coupled with the ability to readily detect and confirm mutations has cemented the role of molecular diagnostics in medicine and, in particular, mutation detection by the polymerase chain reaction (PCR). In PCR Mutation Detection Protocols, Second Edition, expert researchers bring the subject up-to-date with key protocols involving the PCR and its many various incarnations such as SSCP, CSGE, and dHPLC. The volume also addresses key areas such as Southern blotting, accurate diagnostics with high throughput, as well as microarray systems. Written in the highly successful Methods in Molecular Biology™ series format, chapters include brief introductions their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and notes which provide the often hard to find information that may mean the difference between the success and failure of the method.

Authoritative and cutting-edge, PCR Mutation Detection Protocols, Second Edition aims to stimulate postgraduate scientists, researchers, and clinicians already engaged in the area and to provide an important first step for those new to this practice wanting to adopt the powerful and essential technique in their own laboratories.

Conformation Sensitive Capillary Electrophoresis (CSCE).- Conformation Sensitive Gel Electrophoresis.- Denaturing HPLC (dHPLC) for Mutation Screening.- In situ Detection of Human Papillomavirus DNA after PCR-Amplification.- LATE-PCR and Allied Technologies: Real-Time Detection Strategies for Rapid, Reliable Diagnosis from Single Cells.- Long PCR Amplification of Human Genomic DNA.- Human Papilloma Virus Strain Detection Utilizing Custom-Designed Oligonucleotide Microarrays.- Multiplex Ligation-Dependent Probe Amplification (MLPA®) for the Detection of Copy Number Variation in Genomic Sequences.- Screening for Genomic Rearrangements by Multiplex PCR/Liquid Chromatography (MP/LC).- Mutation Surveyor: Software for DNA Sequence Analysis.- Non-Invasive Prenatal Diagnosis (NIPD).- Automated DNA Sequencing.- Phylogenetic Microarrays for Cultivation-Independent Identification and Metabolic Characterization of Microorganisms in Complex Samples.- Prenatal Detection of Chromosome Aneuploidy by Quantitative-Fluorescence PCR.- Use of Robotics in High-Throughput DNA Sequencing.- Detection of Factor V Leiden and Prothrombin c.20210G>A Allele by Roche Diagnostics LightCycler®.- RT-PCR for the Detection of Translocations in Bone and Soft Tissue Tumors in Formalin-Fixed Paraffin-Embedded Tissues.- Detection of Minimal Residual Disease in Leukaemia by RT-PCR.- Mutation Detection by Southern Blotting.

Erscheinungsdatum	19.08.2017
Reihe/Serie	Methods in Molecular Biology ; 688
Zusatzinfo	X, 298 p.
Verlagsort	Totowa, NJ
Sprache	englisch
Maße	178 x 254 mm
Themenwelt	Medizin / Pharmazie ► Medizinische Fachgebiete ► Laboratoriumsmedizin
Themenwelt	Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik
ISBN-10	1-4939-5629-9 / 1493956299
ISBN-13	978-1-4939-5629-6 / 9781493956296
Zustand	Neuware