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41 Questions

Who discovered the Polymerase Chain Reaction (PCR) in 1983?

Kary Mullis

What is the primary purpose of PCR?

To amplify DNA templates

What is the maximum length of DNA segments that can be amplified using PCR?

1000 bp

What is the function of primers in PCR?

To hybridize to the DNA template

What is the temperature used in the denaturation step of PCR?

95°C

How many steps are involved in a PCR cycle?

3

What is the purpose of the elongation step in PCR?

To synthesize DNA

How many cycles are typically performed in a PCR reaction?

25-35

What is the basis of separation of macromolecules in gel electrophoresis?

Size or charge

Why do DNA molecules move towards the positively charged electrode in an electric field?

They are negatively charged

What happens to smaller DNA fragments during gel electrophoresis?

They migrate quickly

How are DNA fragments visualized after gel electrophoresis?

Under UV light with a fluorescent dye

What is the purpose of the power supply in gel electrophoresis?

To provide an electric field

What is the direction of movement of DNA fragments during gel electrophoresis?

From negative to positive electrode

What is the function of the buffer solution in gel electrophoresis?

To maintain the pH of the gel

What determines the migration rate of DNA fragments during gel electrophoresis?

Size of the fragment

What is the first step in cloning DNA?

Cleave the DNA to be cloned with a restriction enzyme

What is the purpose of using a restriction enzyme?

To cut both the plasmid and foreign DNA with complementary sticky ends

What happens when the DNA fragments and cut plasmids are mixed?

They bind together by their sticky ends and link to form recombinant DNA molecules

What is the result of each bacterial cell division?

The plasmid is replicated, producing many copies of the foreign DNA

What is the purpose of selecting cells that contain chimeric plasmids?

To obtain large cultures of cells

What is the final product of gene cloning?

Protein

What is the role of DNA ligase in gene cloning?

To bind the DNA fragments and cut plasmids together

What is the purpose of growing cells under certain conditions?

To allow expression of the cloned gene

What is the purpose of using restriction enzymes in DNA analysis?

To cut the DNA into smaller fragments

What is the function of the buffer in the Southern blotting process?

To transfer the DNA fragments to the filter

What is the purpose of X-ray film in autoradiography?

To visualize the DNA fragments

What is the purpose of the labeled probe in Southern blotting?

To hybridize with the target DNA sequence

What is the result of the gel electrophoresis process?

The DNA fragments are separated by size

What is the purpose of PCR in clinical or forensic testing procedures?

To detect the presence of tumour cells

What is the advantage of using PCR in DNA analysis?

It can amplify specific segments of DNA from a very small sample

What is the application of PCR in diagnosing diseases?

Diagnosis of many inherited diseases

What is the detection capability of PCR in forensic testing?

It can detect the very early stages of pathogenic microorganisms or viruses infection

What is molecular diagnosis?

The process of identifying a disease by studying molecules such as proteins, DNA, and RNA

What is restriction analysis?

A process of cutting DNA molecules into smaller pieces with special enzymes

What are restriction endonucleases?

Bacterial enzymes that cut and recognize double-stranded DNA

What is the purpose of restriction analysis?

To cut DNA molecules into smaller pieces

What is the result of restriction analysis?

Either sticky or blunt ends

What are restriction sites?

Specific sequences recognized by restriction endonucleases

What is the typical length of restriction sites?

4-6 bp

What is the purpose of DNA sequencing?

To analyze DNA at the molecular level

This quiz covers the basics of Polymerase Chain Reaction (PCR), a laboratory technique used to amplify specific DNA sequences. It was discovered by Kary Mullis in 1983 and is used to produce large copies of DNA from small templates. Learn about the components and thermal protocols required for PCR.

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