PCR Technology
Current Innovations, Third Edition
3rd Edition
Published on 26. October 2016
Book
Paperback/Softback
472 pages
978-1-138-19858-6 (ISBN)
Description
PCR's simplicity as a molecular technique is, in some ways, responsible for the huge amount of innovation that surrounds it, as researchers continually think of new ways to tweak, adapt, and re-formulate concepts and applications. PCR Technology: Current Innovations, Third Edition is a collection of novel methods, insights, and points of view that provides a critical and timely reference point for anyone wishing to use this technology.
Topics in this forward-thinking volume include:
The purification and handling of PCR templates
The effect of the manufacture and purification of the oligonucleotide on PCR behavior
Optimum buffer composition
Probe options
The design and optimization of qPCR assays
Issues surrounding the development and refinement of instrumentation
Effective controls to protect against uncertainties due to reaction variability
Covering all aspects of PCR and real-time PCR, the book contains detailed protocols that make it suitable as both a reference and an instruction manual. Each chapter presents detailed guidelines as well as helpful hints and tips supplied by authors who are recognized experts in their fields. In addition to descriptions of current technology and best practices, the book also provides information about new developments in the PCR arena.
Topics in this forward-thinking volume include:
The purification and handling of PCR templates
The effect of the manufacture and purification of the oligonucleotide on PCR behavior
Optimum buffer composition
Probe options
The design and optimization of qPCR assays
Issues surrounding the development and refinement of instrumentation
Effective controls to protect against uncertainties due to reaction variability
Covering all aspects of PCR and real-time PCR, the book contains detailed protocols that make it suitable as both a reference and an instruction manual. Each chapter presents detailed guidelines as well as helpful hints and tips supplied by authors who are recognized experts in their fields. In addition to descriptions of current technology and best practices, the book also provides information about new developments in the PCR arena.
Reviews / Votes
Praise for Previous Editions"This ... second edition provides up-to-date information on PCR technology and applications and covers a selection of widely used procedures and approaches for qualitative as well as quantitative queries. It certainly offers easy to follow, step-by-step protocols and explains the parameters governing PCR reaction outcomes ...
... [A] fundamental reference for scientists new to PCR technology and a source of up-to-date applications for those familiar with the method .... I highly recommend this book as a useful tool for hospital scientists who may use PCR technology in their work; or for scientific researchers .... "
- Australian Journal of Medical Science, Nov. 2004, Vol. 25, No.4 Praise for Previous Editions
"This ... second edition provides up-to-date information on PCR technology and applications and covers a selection of widely used procedures and approaches for qualitative as well as quantitative queries. It certainly offers easy to follow, step-by-step protocols and explains the parameters governing PCR reaction outcomes ...
... [A] fundamental reference for scientists new to PCR technology and a source of up-to-date applications for those familiar with the method .... I highly recommend this book as a useful tool for hospital scientists who may use PCR technology in their work; or for scientific researchers .... "
- Australian Journal of Medical Science, Nov. 2004, Vol. 25, No.4
More details
Edition
3rd edition
Language
English
Place of publication
London
United Kingdom
Publishing group
Taylor & Francis Ltd
Target group
College/higher education
Biochemists and molecular biologists.
Illustrations
138 s/w Abbildungen, 23 farbige Abbildungen, 47 s/w Tabellen
47 Tables, black and white; 23 Illustrations, color; 138 Illustrations, black and white
Dimensions
Height: 254 mm
Width: 178 mm
Thickness: 25 mm
Weight
877 gr
ISBN-13
978-1-138-19858-6 (9781138198586)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Book
06/2013
3rd Edition
CRC Press
€296.40
Shipment within 15-20 days
E-Book
06/2013
3rd Edition
CRC Press
€116.99
Available for download
E-Book
06/2013
3rd Edition
CRC Press
€116.99
Available for download
Persons
Dr. Tania Nolan is an internationally recognized molecular biologist with a reputation for expertise in the field of mRNA quantification using RT-qPCR. She was a significant coauthor of the specialist textbook The A-Z of Quantitative PCR along with numerous other book chapters and peer-reviewed papers. She has presented several plenary lectures and chaired sessions at major international qPCR meetings.
Stephen A. Bustin, BS(Mod) PhD FSB acquired his first qPCR instrument in 1997 and has published numerous peer-reviewed papers that describe and use this technology. He wrote and edited the A-Z of Quantitative PCR, universally acknowledged as the "qPCR Bible," edited The PCR Revolution, and has written a series of Definitive qPCR ebooks. He also led the international consortium that drew up the MIQE guidelines.
Stephen A. Bustin, BS(Mod) PhD FSB acquired his first qPCR instrument in 1997 and has published numerous peer-reviewed papers that describe and use this technology. He wrote and edited the A-Z of Quantitative PCR, universally acknowledged as the "qPCR Bible," edited The PCR Revolution, and has written a series of Definitive qPCR ebooks. He also led the international consortium that drew up the MIQE guidelines.
Content
Template Preparation. Pre-PCR Processing Strategies. Use of a Liposomal Internal Control Vehicle for Whole-Process Quality Assurance of Nucleic Acid Amplification. Reaction Components. Oligonucleotide Synthesis and Purification. Augmenting PCR: Effects of Additives in the Polymerase Chain Reaction. Real-Time Fluorescent PCR by Labeled Primer with a Single Fluorescent Molecule. Using Scorpion Primers for Genotyping. LNA: Adding New Functionality to PCR. Modified dNTPs: A Toolbox for Use in PCR. Instruments. Thermocycler Calibration and Analytical Assay Validation. Ultra-High-Speed PCR Instrument Development. Dropletization of Bioreactions: How Single-Cell Quantitative Analyses May Improve Gene Measurement and Cancer Diagnosis. Design, Optimization, QC, and Standardization. Assay Design for Real-Time qPCR. Primer Design for Large-Scale Multiplex PCR and Arrayed Primer Extension. Development and Use of qPCR Assays for Detection and Study of Neglected Tropical and Emerging Infectious Diseases. MIQE: Guidelines for Reliable Design and Transparent Reporting of Real-Time PCR Assays. Data Analysis. Hypothesis-Driven Approaches to Multivariate Analysis of qPCR Data. Experiment Design, Data Management, and Univariate Statistical Analysis of Gene-Expression Data Obtained by Real-Time Quantitative PCR. Biomarker Discovery via RT-qPCR and Bioinformatical Validation. Optimization of Quantitative Real-Time PCR for Studies in Cartilage Mechanobiology. Applications. Enriching DNA Sequences with Nucleotide Variation by Thymidine Glycosylases Combined with Suppression PCR. Chromosome Walking by Inverse PCR. Expression Profiling of MicroRNAs by Quantitative Real-Time PCR: The Good, the Bad, and the Ugly. Dye-Based High-Throughput qPCR in Microfluidic Platform BioMark (TM). Surface Plasmon Resonance-Based Biosensor Technology for Real-Time Detection of PCR Products. Current Innovations in the Development and Application of the qPCR in a Resource-Limited Setting. A Review of Isothermal Nucleic Acid Amplification Technologies. Proximity Ligation Assay for Protein Quantification. High-Resolution Melt Analysis. Index.