Literature DB >> 7920237

Improved quantitative PCR using nested primers.

L A Haff1.   

Abstract

Quantitative PCR can often be improved by conducting the amplification with nested primers. First, fewer nonspecific amplification products, which could otherwise interfere with quantitation, are produced. Often, nonspecific products can be eliminated. In these cases, relatively simple nonspecific detection techniques are suitable for quantitation. In addition, nested primer PCR provides intrinsic PCR product carryover protection and generally improves the robustness and lower limit of detection of PCR. For a nested PCR to provide useful quantitative information, it is important that the initial phase of amplification, performed with the outer pair of primers, takes place entirely in the exponential phase. This is generally achieved easily. The major consideration in designing a nested PCR protocol compatible with quantitation is to assure that the maximum concentration of PCR products produced by the outer primers does not exceed approximately 10% the molarity of the outer primers. A simple formula can be used to determine the maximum number of thermal cycles that provide this assurance. Good correspondence was obtained between initial target concentration and final PCR product yield in a nested-primer HIV-1 PCR.

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Year:  1994        PMID: 7920237     DOI: 10.1101/gr.3.6.332

Source DB:  PubMed          Journal:  PCR Methods Appl        ISSN: 1054-9803


  16 in total

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4.  Sensitive detection of Ehrlichia chaffeensis in cell culture, blood, and tick specimens by reverse transcription-PCR.

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Journal:  J Clin Microbiol       Date:  2001-02       Impact factor: 5.948

5.  Single-cell Gene Expression Profiling Using FACS and qPCR with Internal Standards.

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Authors:  Yongchun Wang; Alan K Meeker; Jeanne Kowalski; Hua-Ling Tsai; Helina Somervell; Christopher Heaphy; Lauren E Sangenario; Nijaguna Prasad; William H Westra; Martha A Zeiger; Christopher B Umbricht
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7.  Complementary change in cis determinants and trans factors in the evolution of an mRNP stability complex.

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8.  Differentiating alternative splice variant patterns of human telomerase reverse transcriptase in thyroid neoplasms.

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Journal:  Thyroid       Date:  2008-10       Impact factor: 6.568

9.  CMV-DNA detection in parenchymatous organs in cases of SIDS.

Authors:  R Cecchi; T Bajanowski; B Kahl; P Wiegand
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10.  An ospA-polymerase chain reaction/restriction fragment length polymorphism-based method for sensitive detection and reliable differentiation of all European Borrelia burgdorferi sensu lato species and OspA types.

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Journal:  Med Microbiol Immunol       Date:  2003-09-12       Impact factor: 3.402

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