Literature DB >> 1571142

PCR: how to kill unwanted DNA.

A M Prince1, L Andrus.   

Abstract

Avoidance of contamination in the PCR laboratory requires the use of strict precautions. Among these, chemical decontamination of surfaces and equipment is desirable to prevent inadvertent contamination of samples by the gloved hand and by pipettors. We have investigated the use of sodium hypochloride (Clorox), in comparison to concentrated HCl, for PCR sterilization. Ten percent Clorox was found to eliminate all ethidium bromide-stainable DNA and to prevent PCR amplification of a 600-bp DNA segment within one minute of template treatment. RNA was similarly destroyed. By contrast, even 2.0 N HCl did not destroy DNA detectable by PCR within five minutes. Because of its high efficacy, low cost and relatively low corrosiveness, we recommend the use of ten percent Clorox as a decontaminant for elimination of DNA templates in the PCR laboratory.

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Year:  1992        PMID: 1571142

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


  35 in total

1.  An mtDNA analysis in ancient Basque populations: implications for haplogroup V as a marker for a major paleolithic expansion from southwestern europe.

Authors:  N Izagirre; C de la Rúa
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

Review 2.  Molecular diagnostics in preimplantation genetic diagnosis.

Authors:  Alan R Thornhill; Karen Snow
Journal:  J Mol Diagn       Date:  2002-02       Impact factor: 5.568

Review 3.  Advances in nucleic acid-based detection methods.

Authors:  M J Wolcott
Journal:  Clin Microbiol Rev       Date:  1992-10       Impact factor: 26.132

Review 4.  False-positive results and contamination in nucleic acid amplification assays: suggestions for a prevent and destroy strategy.

Authors:  A Borst; A T A Box; A C Fluit
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2004-03-10       Impact factor: 3.267

Review 5.  Inhibition and facilitation of nucleic acid amplification.

Authors:  I G Wilson
Journal:  Appl Environ Microbiol       Date:  1997-10       Impact factor: 4.792

6.  Problems of reproducibility--does geologically ancient DNA survive in amber-preserved insects?

Authors:  J J Austin; A J Ross; A B Smith; R A Fortey; R H Thomas
Journal:  Proc Biol Sci       Date:  1997-04-22       Impact factor: 5.349

7.  Sporicidal efficacy of pH-adjusted bleach for control of bioburden on production facility surfaces.

Authors:  Anne Cornish Frazer; Josephine N Smyth; Vishvesh K Bhupathiraju
Journal:  J Ind Microbiol Biotechnol       Date:  2013-03-27       Impact factor: 3.346

8.  Comparison of multiplex PCR assay with culture for detection of genital mycoplasmas.

Authors:  Kathleen A Stellrecht; Amy M Woron; Nada G Mishrik; Richard A Venezia
Journal:  J Clin Microbiol       Date:  2004-04       Impact factor: 5.948

9.  A more reliable PCR for detection of Mycobacterium tuberculosis in clinical samples.

Authors:  L F Kox; D Rhienthong; A M Miranda; N Udomsantisuk; K Ellis; J van Leeuwen; S van Heusden; S Kuijper; A H Kolk
Journal:  J Clin Microbiol       Date:  1994-03       Impact factor: 5.948

10.  An efficient multistrategy DNA decontamination procedure of PCR reagents for hypersensitive PCR applications.

Authors:  Sophie Champlot; Camille Berthelot; Mélanie Pruvost; E Andrew Bennett; Thierry Grange; Eva-Maria Geigl
Journal:  PLoS One       Date:  2010-09-28       Impact factor: 3.240

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