PCR Amplification Formula:
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PCR (Polymerase Chain Reaction) is a technique used to amplify specific DNA sequences exponentially. Each cycle theoretically doubles the amount of target DNA.
The calculator uses the PCR amplification formula:
Where:
Explanation: The equation accounts for exponential growth of DNA copies during PCR, where each cycle doubles the DNA amount.
Details: Accurate DNA quantification is crucial for molecular biology experiments, diagnostic testing, and research applications.
Tips: Enter the initial number of DNA copies and the number of PCR cycles. Both values must be positive integers.
Q1: Is the doubling perfect in real PCR?
A: No, actual amplification may be less efficient due to reaction limitations, typically reaching a plateau phase.
Q2: What's a typical number of PCR cycles?
A: Most protocols use 25-40 cycles, with 30 being common for many applications.
Q3: How many copies are needed for detection?
A: Most detection methods can detect 10^6-10^9 copies, but highly sensitive methods can detect fewer.
Q4: What affects PCR efficiency?
A: Primer design, template quality, enzyme performance, and reaction conditions all impact efficiency.
Q5: Can this calculator be used for qPCR?
A: This calculates theoretical maximum, while qPCR accounts for actual amplification efficiency.