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A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res

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by Michaelw. Pfaffl
Citations:1085 - 4 self
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BibTeX

@MISC{Pfaffl_anew,
    author = {Michaelw. Pfaffl},
    title = {A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res},
    year = {}
}

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Abstract

Use of the real-time polymerase chain reaction (PCR) to amplify cDNA products reverse transcribed from mRNA is on the way to becoming a routine tool in molecular biology to study low abundance gene expression. Real-time PCR is easy to perform, provides the necessary accuracy and produces reliable as well as rapid quantification results. But accurate quantification of nucleic acids requires a reproducible methodology and an adequate mathematical model for data analysis. This study enters into the particular topics of the relative quantification in real-time RT–PCR of a target gene transcript in comparison to a reference gene transcript. Therefore, a new mathematical model is presented. The relative expression ratio is calculated only from the real-time PCR efficiencies and the crossing point deviation of an unknown sample versus a control. This model needs no calibration curve. Control levels were included in the model to standardise each reaction run with respect to RNA integrity, sample loading and inter-PCR variations. High accuracy and reproducibility (<2.5 % variation) were reached in LightCycler PCR using the established mathematical model.

Keyphrases

new mathematical model    relative quantification    real-time rt-pcr    nucleic acid re    target gene transcript    crossing point deviation    control level    accurate quantification    sample loading    high accuracy    inter-pcr variation    cdna product    real-time rt pcr    real-time pcr efficiency    reproducible methodology    data analysis    molecular biology    unknown sample    lightcycler pcr    mathematical model    routine tool    real-time pcr    relative expression ratio    real-time polymerase chain reaction    particular topic    reference gene transcript    necessary accuracy    low abundance gene expression    rna integrity    rapid quantification result    adequate mathematical model    calibration curve    nucleic acid   

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