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Author | : C. Simon Herrington |
Publisher | : Oxford University Press |
Total Pages | : 223 |
Release | : 1997-10-30 |
Genre | : Science |
ISBN | : 0191565598 |
PCR in situ hybridization allows the detection of specific nucleic acid sequences and their distribution in the cell. It combines two powerful techniquesin situ hybridization (ISH), which allows cellular localization of DNA and RNA sequences in cells and tissues, and the polymerase chain reaction (PCR), which allows reproducible amplification of rare nucleic acid sequences. The combined technique and its variants greatly enhance the sensitivity of in situ hybridization and add morphological localization to the sensitivity of PCR. Such techniques have enormous potential for research and diagnosis but problems with reproducibility and reliability are often encountered. This book overcomes these problems by describing the key procedures in step-by-step detail and by providing the essential advice needed for success. Topics include: DNA in situ PCR and DNA PCR in situ hybridization (PCR ISH) for the detection of DNA targets in cells; reverse trancriptase in situ PCR (RT-PCR) and RT-PCR ISH for the detection of RNA targets; and PRINS (primed in situ synthesis) for chromosomal analysis in interphase nuclei and metaphase chromosome spreads. There are further chapters on fixation of tissues for PCR, selective ultraviolet radiation fractionation (SURF), application of in situ PCR to human tissues, applications and modifications of PCR-ISH, and automation of in situ amplification. PCR In Situ Hybridization is a unique and timely collection of well-tested protocols for the amplification of DNA and RNA in cells and tissues, drawing on the accumulated knowledge and experience of leading exponents of these techniques. For each topic covered, the authors provide detailed guidance on the key steps in the protocols, numerous hints and tips for success, and advice on trouble-shooting. PCR In Situ Hybridization will be invaluable to molecular biologists, pathologists, geneticists, and all those seeking to perform in situ analyses of nucleic acid molecules.
Author | : George Ross Hull |
Publisher | : |
Total Pages | : 638 |
Release | : 1919 |
Genre | : Corporation law |
ISBN | : |
Containing opinions, general orders, administrative rulings, reports, circulars, rules of practice, rules and regulations of service, etc., of the Public Service Commission of Pennsylvania; and opinions of the county courts throughout the Commonwealth and of the attorney general involving the law of private corporations, including corporation tax cases and appeals from the Public Service Commission; and index and annotations to the Public service company law.
Author | : Pennsylvania |
Publisher | : |
Total Pages | : 962 |
Release | : 1915 |
Genre | : Corporation law |
ISBN | : |
Author | : Stephen A. Bustin |
Publisher | : Cambridge University Press |
Total Pages | : 327 |
Release | : 2010 |
Genre | : Science |
ISBN | : 0521882311 |
Examines the latest innovations and the overall impact of PCR on areas of molecular research.
Author | : John M. S. Bartlett |
Publisher | : Springer Science & Business Media |
Total Pages | : 1083 |
Release | : 2008-02-03 |
Genre | : Science |
ISBN | : 1592593844 |
In this new edition, the editors have thoroughly updated and dramatically expanded the number of protocols to take advantage of the newest technologies used in all branches of research and clinical medicine today. These proven methods include real time PCR, SNP analysis, nested PCR, direct PCR, and long range PCR. Among the highlights are chapters on genome profiling by SAGE, differential display and chip technologies, the amplification of whole genome DNA by random degenerate oligonucleotide PCR, and the refinement of PCR methods for the analysis of fragmented DNA from fixed tissues. Each fully tested protocol is described in step-by-step detail by an established expert in the field and includes a background introduction outlining the principle behind the technique, equipment and reagent lists, tips on trouble shooting and avoiding known pitfalls, and, where needed, a discussion of the interpretation and use of results.
Author | : George Ross Hull |
Publisher | : |
Total Pages | : 1976 |
Release | : 1915 |
Genre | : Corporation law |
ISBN | : |
Containing opinions, general orders, administrative rulings, reports, circulars, rules of practice, rules and regulations of service, etc., of the Public Service Commission of Pennsylvania; and opinions of the county courts throughout the Commonwealth and of the attorney general involving the law of private corporations, including corporation tax cases and appeals from the Public Service Commission; and index and annotations to the Public service company law.
Author | : Mike McPherson |
Publisher | : Garland Science |
Total Pages | : 292 |
Release | : 2007-01-25 |
Genre | : Science |
ISBN | : 0203002679 |
A thoroughly updated version of the successful first edition with a new chapter on Real-Time PCR, more prokaryotic applications, and more detail in the complex mutagenesis sections. Information on PCR applications in genomics and proteomics have been expanded and integrated throughout the text. There is also advice on available products and specific pointers to the most appropriate methods. As with the first edition, this will be an ideal practical introduction and invaluable guide to PCR and its applications.
Author | : Tania Nolan |
Publisher | : CRC Press |
Total Pages | : 447 |
Release | : 2013-06-13 |
Genre | : Law |
ISBN | : 1439848130 |
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
Author | : Bing-Yuan Chen |
Publisher | : Springer Science & Business Media |
Total Pages | : 429 |
Release | : 2008-02-05 |
Genre | : Science |
ISBN | : 1592591779 |
PCR Cloning Protocols, Second Edition, updates and expands Bruce White's best-selling PCR Cloning Protocols (1997) with the newest procedures for DNA cloning and mutagenesis. Here the researcher will find readily reproducible methods for all the major aspects of PCR use, including PCR optimization, computer programs for PCR primer design and analysis, and novel variations for cloning genes of special characteristics or origin, with emphasis on long distance PCR and GC-rich template amplification. Also included are both conventional and novel enzyme-free and restriction site-free procedures to clone PCR products into a range of vectors, as well as state-of-the-art protocols to facilitate DNA mutagenesis and recombination, and to clone the challenging uncharacterized DNA flanking a known DNA fragment.
Author | : Nicola King |
Publisher | : Springer Science & Business Media |
Total Pages | : 370 |
Release | : 2008-02-04 |
Genre | : Science |
ISBN | : 159259283X |
Until the mid 1980s, the detection and quantification of a specific mRNA was a difficult task, usually only undertaken by a skilled molecular biologist. With the advent of PCR, it became possible to amplify specific mRNA, after first converting the mRNA to cDNA via reverse transcriptase. The arrival of this technique—termed reverse transcription-PCR (RT-PCR)—meant that mRNA suddenly became amenable to rapid and sensitive analysis, without the need for advanced training in molecular biology. This new accessibility of mRNA, which has been facilitated by the rapid accumulation of sequence data for human mRNAs, means that every biomedical researcher can now include measurement of specific mRNA expression as a routine component of his/her research plans. In view of the ubiquity of the use of standard RT-PCR, the main objective of RT-PCR Protocols is essentially to provide novel, useful applications of RT-PCR. These include some useful adaptations and applications that could be relevant to the wider research community who are already familiar with the basic RT-PCR protocol. For example, a variety of different adaptations are described that have been employed to obtain quantitative data from RT-PCR. Quantitative RT-PCR provides the ability to accurately measure changes/imb- ances in specific mRNA expression between normal and diseased tissues.