Polymerase Chain Reaction (PCR) amplifies DNA through three primary steps:
• Denaturation: Heating DNA to 95°C separates double-stranded DNA into two single strands.
• Annealing: The temperature drops to 50-65°C, allowing primers to bind to complementary DNA sequences.
• Extension: At 72°C (optimal for Taq DNA Polymerase), DNA polymerase synthesizes new strands by adding nucleotides to the primers.
These steps are cyclically repeated to amplify target DNA regions. The sequence is Denaturation > Annealing > Extension.
| List-I | List-II |
|---|---|
| (A) Alkaline phosphatase | (i) Removes phosphate group at 5’ end of DNA |
| (B) DNA Polymerase | (ii) Nick translation |
| (C) SI Nuclease | (iii) Cleaves ssDNA |
| (D) DNase I | (iv) Cleaves DNA |
| List-I | List-II |
|---|---|
| (A) IgA | (i) Basophils |
| (B) IgE | (ii) Secretory components |
| (C) IgG | (iii) Pentamer |
| (D) IgM | (iv) Crosses Placenta |