Should always be more than 50 nucleotides in length
Secondary structures such as hairpins
Sequences with stretches of identical single nucleotides
Minimal complementarity between reverse and forward primers
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The Correct Option isD
Solution and Explanation
Concept:
PCR primers must be designed carefully to ensure efficient and specific amplification.
Step 1: Ideal primer characteristics.
• Length: typically 18--25 nucleotides
• No secondary structures (like hairpins)
• No long stretches of identical bases
• Minimal complementarity between primers (to avoid primer-dimers)
Step 2: Analyze options.
• (A) Incorrect → Too long (not ideal)
• (B) Incorrect → Hairpins reduce efficiency
• (C) Incorrect → Repeats cause mispriming
• (D) Correct → Prevents primer-dimer formation
Step 3: Final conclusion.
Thus, the desirable feature is:
\[
Minimal complementarity between forward and reverse primers
\]