Answer :
the correct sequence of temperatures for a typical PCR reaction is 94°C, 50-60°C, and 72-74°C, corresponding to denaturation, annealing, and extension, respectively.
During PCR (polymerase chain reaction), the reaction mixture is subjected to a series of temperature changes, each optimized for specific biochemical reactions to occur. These temperature changes are usually carried out in a thermal cycler, a machine that can rapidly cycle through the different temperature steps.
The typical sequence of temperatures in a PCR reaction is:
- Denaturation: at a temperature of around 94-98°C, the double-stranded DNA template is denatured, separating the two strands from each other.
- Annealing: at a temperature of around 50-60°C, the primers anneal (bind) to the complementary single-stranded template DNA at the target sequence.
- Extension: at a temperature of around 72-74°C, the Taq polymerase enzyme extends the primers by adding nucleotides to the 3' end of the primer, synthesizing a new strand of DNA that is complementary to the template strand.
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