Concept:
Polymerase Chain Reaction (PCR) is an in vitro technique used to amplify a specific DNA sequence. During every PCR cycle, the amount of DNA approximately doubles because each newly synthesized DNA strand serves as a template in the next cycle.
• PCR was developed by Kary Mullis.
• It consists of three major steps:
• Denaturation
• Annealing
• Extension
• Each cycle ideally doubles the DNA molecules.
• Therefore, DNA amplification follows an exponential pattern.
Step 1: Understand DNA amplification.
Suppose one DNA template molecule is present initially.
After each PCR cycle:
\[
\begin{aligned}
1^{st}\ \text{cycle} &\rightarrow 2 \\
2^{nd}\ \text{cycle} &\rightarrow 4 \\
3^{rd}\ \text{cycle} &\rightarrow 8 \\
4^{th}\ \text{cycle} &\rightarrow 16
\end{aligned}
\]
Thus the DNA quantity doubles every cycle.
Step 2: Derive the general formula.
If amplification efficiency is assumed to be 100%, then after \(n\) cycles,
\[
\boxed{\text{Number of DNA molecules}=2^{n}}
\]
For example,
\[
10\ \text{cycles}=2^{10}=1024\ \text{DNA molecules}
\]
\[
30\ \text{cycles}=2^{30}\approx1.07\times10^{9}\ \text{copies}
\]
Hence PCR can generate millions to billions of DNA copies within a few hours.
Step 3: Choose the correct option.
Therefore,
\[
\boxed{Option (A) 2^{n} is the correct answer.
\]