Polymerase Chain Reaction Techniques Quiz

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20 Questions

What is the purpose of the polymerase chain reaction (PCR)?

To rapidly make millions to billions of copies of a specific DNA sample

At what temperature is the denaturation of dsDNA template performed in PCR?

92–95°C

What is the function of Deoxynucleoside triphosphates (dNTPs) in PCR?

To serve as energy sources for DNA synthesis

Which chemical component of PCR is responsible for reducing the energy barrier during DNA synthesis?

MgCl2

What is the main function of thermostable DNA polymerase in PCR?

To add nucleotides to the growing DNA strand

What is the purpose of PCR primers in the polymerase chain reaction (PCR)?

To initiate DNA synthesis in PCR by matching the sequences at the ends of or within the target DNA

What is the purpose of the denaturation step in PCR?

To disrupt the hydrogen bonds between complementary bases, yielding single-stranded DNA molecules

What is the function of Multiplex PCR?

To produce amplicons of varying sizes that are specific to different DNA sequences

What is the purpose of the extension/elongation step in PCR?

To synthesize a new DNA strand complementary to the DNA template strand by adding dNTPs in 3' to 5' direction

What is the significance of the initialization step in PCR?

It heats the reaction to a temperature required for heat activation of DNA polymerases

PCR is a method used to make millions to billions of copies of a specific RNA sample.

False

PCR is not commonly used in medical laboratory research for applications in biomedical research and criminal forensics.

False

The denaturation of dsDNA template in PCR is performed at approximately 100°C.

False

PCR does not involve amplifying copies of very small amounts of DNA sequences in a series of cycles of temperature changes.

False

PCR primers are not one of the chemical components of PCR.

False

During the denaturation step in PCR, hydrogen bonds between complementary bases are strengthened, leading to the formation of double-stranded DNA molecules.

False

Hot-start PCR is initiated at a temperature of 94–96 °C to activate extremely thermostable polymerases.

True

Multiplex PCR involves amplifying only a single DNA sequence at a time to produce amplicons of varying sizes.

False

The annealing step in PCR involves lowering the reaction temperature to 70–75 °C for 30–40 seconds.

False

Touchdown PCR is a type of PCR that initially has a high annealing temperature which is gradually decreased in subsequent cycles.

True

Test your knowledge on nucleic acid extraction and the polymerase chain reaction (PCR) techniques used to rapidly make millions to billions of copies of a specific DNA sample.

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