(Q24793641)

English

Quantitative assessment of the effect of uracil-DNA glycosylase on amplicon DNA degradation and RNA amplification in reverse transcription-PCR

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Quantitative assessment of the effect of uracil-DNA glycosylase on amplicon DNA degradation and RNA amplification in reverse transcription-PCR (English)

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Steven B Kleiboeker

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publication date

2005

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Virology Journal

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2

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1

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29

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Multiplex PCR: optimization and application in diagnostic virology

1 reference

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Applications of Competitor RNA in Diagnostic Reverse Transcription-PCR

1 reference

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7 April 2017

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

1 reference

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7 April 2017

Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactions

1 reference

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7 April 2017

Avoiding false positives with PCR

1 reference

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PCR-based diagnostics for infectious diseases: uses, limitations, and future applications in acute-care settings

1 reference

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28 September 2017

Nucleic acid approaches for detection and identification of biological warfare and infectious disease agents

1 reference

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28 September 2017

Update on molecular techniques for diagnostic testing of infectious disease

1 reference

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28 September 2017

Direct hybridization and amplification applications for the diagnosis of infectious diseases

1 reference

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28 September 2017

Preventing false positives: quantitative evaluation of three protocols for inactivation of polymerase chain reaction amplification products

1 reference

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28 September 2017

A novel method employing UNG to avoid carry-over contamination in RNA-PCR.

1 reference

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28 September 2017

Use of modified nucleotides and uracil-DNA glycosylase (UNG) for the control of contamination in the PCR-based amplification of RNA.

1 reference

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30 May 2018

Simultaneous detection of North American and European porcine reproductive and respiratory syndrome virus using real-time quantitative reverse transcriptase-PCR.

1 reference

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Effectiveness and limitations of uracil-DNA glycosylases in sensitive real-time PCR assays.

1 reference

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Use of heat labile UNG in an RT-PCR assay for enterovirus detection

1 reference

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28 November 2018

Optimized PCR amplification of influenza A virus RNA using Tth DNA polymerase, incorporating uracil N glycosylase (UNG) in a single tube reaction.

1 reference

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Heat-labile uracil-DNA glycosylase: purification and characterization.

1 reference

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28 November 2018

Sensitive and robust one-tube real-time reverse transcriptase-polymerase chain reaction to quantify SIV RNA load: comparison of one- versus two-enzyme systems

1 reference

https://pubmed.ncbi.nlm.nih.gov/15823209

12 December 2020

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10.1186/1743-422X-2-29

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9 September 2019

https://scigraph.springernature.com/pub.10.1186/1743-422x-2-29

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