Literature DB >> 2223067

Thermocycler temperature variation invalidates PCR results.

U Linz1.   

Abstract

Among the factors which have to be optimized to ensure highest sensitivity and specificity of the polymerase chain reaction (PCR) is the processor which enables the automatic performance of the PCR assay. It has to guarantee temperature homogeneity for all samples of an individual run and run-to-run comparability. The following report illustrates that the present generation of PCR processors does not yet fulfill this requirement to satisfaction. It discusses examples of significant performance variations and their consequences for the outcome of the amplification reaction.

Mesh:

Year:  1990        PMID: 2223067

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  8 in total

Review 1.  Molecular biology made easy. The polymerase chain reaction.

Authors:  A M Clarke; N P Mapstone; P Quirke
Journal:  Histochem J       Date:  1992-12

2.  Novel approach for assessing performance of PCR cyclers used for diagnostic testing.

Authors:  D Schoder; A Schmalwieser; G Schauberger; J Hoorfar; M Kuhn; M Wagner
Journal:  J Clin Microbiol       Date:  2005-06       Impact factor: 5.948

3.  Factors affecting reliability and reproducibility of amplification-based DNA fingerprinting of representative bacterial pathogens.

Authors:  K D Tyler; G Wang; S D Tyler; W M Johnson
Journal:  J Clin Microbiol       Date:  1997-02       Impact factor: 5.948

4.  Quantification of Coxiella burnetii by polymerase chain reaction (PCR) and a colorimetric microtiter plate hybridization assay (CMHA).

Authors:  E Fritz; D Thiele; H Willems; M M Wittenbrink
Journal:  Eur J Epidemiol       Date:  1995-10       Impact factor: 8.082

5.  Double-step PCR assay to quantify Epstein-Barr viral load in peripheral blood.

Authors:  Massimiliano Bergallo; Chiara Merlino; Roberta Daniele; Franca Sinesi; Mara Fumagalli; Alessandro Negro Ponzi; Rossana Cavallo
Journal:  Mol Biotechnol       Date:  2004-07       Impact factor: 2.695

6.  Quantitative PCR for human herpesviruses 6 and 7.

Authors:  P Secchiero; D Zella; R W Crowley; R C Gallo; P Lusso
Journal:  J Clin Microbiol       Date:  1995-08       Impact factor: 5.948

7.  Differentiation of Fusarium solani f. sp. cucurbitae races 1 and 2 by random amplification of polymorphic DNA.

Authors:  R N Crowhurst; B T Hawthorne; E H Rikkerink; M D Templeton
Journal:  Curr Genet       Date:  1991-11       Impact factor: 3.886

Review 8.  Considerations for accurate gene expression measurement by reverse transcription quantitative PCR when analysing clinical samples.

Authors:  Rebecca Sanders; Deborah J Mason; Carole A Foy; Jim F Huggett
Journal:  Anal Bioanal Chem       Date:  2014-05-25       Impact factor: 4.142

  8 in total

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