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DNA Extraction & Gel Electrophoresis

Total questions: 16

Worksheet time: 5mins

Name
Class
Date
1.

DNA extraction requires _________to lyse the epithelial cells and to degrade compounds inhibitory to amplification

a)

freezing

b)

heat treatment

c)

enzyme

d)

mechanical shearing

2.

What can you observe on the agarose gel after electrophoresis if you do not treat your sample with RNAse ?

a)

protein

b)

RNA

c)

mitochondria

d)

phospholipids

3.

The ratio of absorption at 260nm to absorption at 280nm is commonly used to assess….

a)

Whether your DNA or RNA is contaminated with organic substances.

b)

The purity of DNA and RNA with respect to protein.

c)

The concentration of protein in your sample.

4.

Put the following types of naturally occurring RNA in order according to their abundance in cellular or total RNA. (First listed is most abundant)

a)

mRNA, rRNA, tRNA

b)

rRNA, tRNA, mRNA

c)

tRNA, rRNA, mRNA

d)

tRNA, mRNA, rRNA

5.

When evaluating the purity of extracted DNA, deoxyribonucleic acid, what should the optical density, or its light-blocking ability, be at 260nm and 280nm be? (The 260nm/280nm ratio)

a)

< 1.6

b)

2.0 - 2.3

c)

>2.0

d)

1.6 - 2.0

6.

What is the purpose of a buffer system in electrophoresis?

a)

Alternate the current

b)

Carry the current, maintain a stable pH for the separation of molecules and protect the sample

c)

disrupt the contaminants

d)

stop the migration process

7.

How can DNA fragments be separated using gel electrophoresis ?

a)

DNA carries a negative charge and large fragments are pulled more strongly than small fragments towards the positive electrode

b)

DNA carries a negative charge and small fragments are able to travel more quickly than large towards the positive electrode

c)

DNA carries a positive charge and large fragments are pulled more strongly than small fragments towards the negative electrode

d)

DNA carries a positive charge and small fragments are able to travel more quickly than large towards the negative electrode

8.

Where would you find DNA, the genetic material, in an animal cell?

a)

In the centriole

b)

Only in the mitochondria

c)

In the mitochondria and the nucleus

d)

In the cytoplasm

9.

Eukaryotic chromosomes are thousands of times longer than a typical cell. How can chromosomes fit inside a eukaryotic nucleus?

a)

The genetic material remains distributed in the nucleus, mitochondria, and chloroplast.

b)

The genome is present in a looped structure; thus, it fits the size of the nucleus.

c)

The DNA remains coiled around proteins to form nucleosomes.

d)

The genetic material remains bound to the nuclear envelope, forming invaginations.

10.

What is the first step in isolating DNA?

a)

Generating genomic DNA fragments with restriction endonucleases

b)

Introducing recombinant DNA into an organism by any means

c)

Overexpressing proteins in E. coli

d)

Lysing the cells in the sample

11.

What is the role of ethanol in DNA extraction?

a)

To break down cell walls

b)

To precipitate DNA from the solution

c)

To neutralize the pH

d)

To increase the solubility of the DNA

12.

The basic principle behind separating DNA from a cell lysate relies on the difference in properties between:

a)

Nucleic acid and proteins

b)

Proteins and lipids

c)

DNA & RNA

d)

Nucleotides & enzyme

13.

Silica membranes in DNA extraction columns primarily bind to which molecule based on its charge?

a)

DNA

b)

Protein

c)

Enzyme

d)

Lipid

14.

Which of the following statements accurately describes the role of centrifugation in DNA extraction?

a)

It lyses the cells to release DNA.

b)

It selectively precipitates DNA from the solution.

c)

It separates DNA fragments based on size.

d)

It separates heavier cellular components from the DNA suspension.

15.

What is the main purpose of a wash buffer used with silica membrane columns?

a)

lyse cells and release DNA

b)

remove proteins and other contaminants

c)

elute purified DNA from the column

d)

precipitate DNA from solution

16.

During elution in silica membrane column extraction, what property allows DNA to be released from the membrane?

a)

High ionic strength of the elution buffer

b)

Lower affinity of DNA for the membrane at low ionic strength

c)

Change in pH of the elution buffer

d)

Heat treatment of the column