000			04000nam a22005055i 4500
001			978-1-4020-6241-4
003			DE-He213
005			20251006084530.0
007			cr nn 008mamaa
008			100301s2008 ne | s |||| 0|eng d
020			_a9781402062414
020			_a99781402062414
024	7		_a10.1007/978-1-4020-6241-4 _2doi
082	0	4	_a570 _223
100	1		_aPelt-Verkuil, Elizabeth. _eauthor.
245	1	0	_aPrinciples and Technical Aspects of PCR Amplification _h[electronic resource] / _cby Elizabeth Pelt-Verkuil, Alex Belkum, John P. Hays.
264		1	_aDordrecht : _bSpringer Netherlands, _c2008.
300			_bonline resource.
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
347			_atext file _bPDF _2rda
505	0		_aThe Polymerase Chain Reaction -- A Brief Comparison Between In Vivo DNA Replication and In Vitro PCR Amplification -- The PCR in Practice -- The Different Types and Varieties of Nucleic Acid Target Molecules -- PCR Primers -- Deoxynucleotide Triphosphates and Buffer Components -- Taq and Other Thermostable DNA Polymerases -- Important Considerations for Typical, Quantitative and Real-Time PCR Protocols -- Analysis of PCR Amplification Products -- Ensuring PCR Quality - Laboratory Organisation, PCR Optimization and Controls -- Ensuring PCR Quality - Quality Criteria and Quality Assurance -- Variants and Adaptations of the Standard PCR Protocol -- In Situ PCR Amplification (ISA) - Major Considerations, Sample Processing and Applications.
520			_aKary Mullis was awarded a Nobel Prize for inventing the PCR technique more than 15 years ago in 1993. Since its "discovery", multiple adaptations and variations of the standard PCR technique have been described, with many of these adaptations and variations currently being used in clinical, diagnostic and academic laboratories across the world. Further, these techniques are being applied at the diagnostic level (e.g. as high throughput testing methodologies to detect minimum residual disease, the presence/absence of specific pathogens etc), as well as to increase our understanding of fundamental disease processes. Frequently, PCR technicians and specialists limit their understanding of PCR to one particular methodology. However, this approach limits their appreciation of the range of versatile PCR techniques currently available, techniques that may be applicable and indeed more suitable to their own laboratory situation. This manual aims to provide the reader with a guide to the standard PCR technique and its many available modifications, with particular emphasis on the role of PCR techniques in the diagnostic laboratory (the central theme of this manual). Further, many important technical issues have been addressed, including types of PCR template material, PCR optimization, the analysis of PCR products, quality control and quality assurance, variants and adaptations of the standard PCR protocol, quantitative PCR and in situ PCR. The reader of this manual will be excellently informed about the fundamental principles of PCR and the true potential of PCR within clinical laboratory practice.
650		0	_aLIFE SCIENCES.
650		0	_aMEDICINE.
650		0	_aBIOCHEMISTRY.
650		0	_aCYTOLOGY.
650		0	_aCYTOLOGY _xRESEARCH_XMETHODOLOGY.
650	1	4	_aLIFE SCIENCES.
650	2	4	_aLIFE SCIENCES, GENERAL.
650	2	4	_aBIOMEDICINE GENERAL.
650	2	4	_aBIOCHEMISTRY, GENERAL.
650	2	4	_aCELL BIOLOGY.
650	2	4	_aBIOLOGICAL TECHNIQUES.
700	1		_aBelkum, Alex. _eauthor.
700	1		_aHays, John P. _eauthor.
710	2		_aSpringerLink (Online service)
773	0		_tSpringer eBooks
776	0	8	_iPrinted edition: _z9781402062407
856	4	0	_uhttp://dx.doi.org/10.1007/978-1-4020-6241-4 _zVer el texto completo en las instalaciones del CICY
912			_aZDB-2-SBL
942			_2ddc _cER
999			_c61631 _d61631