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In quantitative PCR (qPCR), amplification of the target DNA is typically visualized as a rapid exponential increase during the early cycles of the reaction. This exponential phase occurs because DNA replication occurs at a much faster rate when there are sufficient reagents and optimal conditions present. As the PCR cycles continue, the amount of target DNA doubles with each cycle, leading to a steep rise in the signal detected by the qPCR machine.
The exponential increase in fluorescence signal directly correlates with the amount of the target DNA, allowing for quantification of the initial template concentration. This is crucial for accurate measurement and comparison across samples. Once the reaction reaches a certain threshold, the amplification may not continue at the same exponential rate due to depletion of reagents or other limiting factors, leading to a plateau phase that reflects decreased rates of amplification.
Understanding this pattern is key for interpreting qPCR results, as the linear phase following the exponential phase and the subsequent plateau are less useful for quantification purposes compared to the initial rapid exponential increase which represents the most reliable phase for determining the starting quantity of the target nucleic acid.