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ELISA Quiz Part 1

Total questions: 24

Worksheet time: 12mins

Name
Class
Date
1.

What does ELISA stand for?

a)

Enzyme Linked Immunosorbent Assay

b)

Enzyme Linked Immunosuppressant Assay

c)

Enzyme Linked Immunoglobulin Assay

d)

Enzyme Linked Immunoassay

2.

What is the purpose of the solid phase in ELISA?

a)

To provide a surface for antigen/antibody attachment

b)

To enhance the color reaction

c)

To dilute the enzyme

d)

To increase the temperature

3.

What is adsorption in the context of ELISA?

a)

The process of adding an antigen/antibody to a solid phase

b)

The process of removing antibodies from a solution

c)

The process of heating the enzyme

d)

The process of changing the pH of the solution

4.

What is the role of washing in ELISA?

a)

To separate bound from unbound reagents

b)

To increase the enzyme activity

c)

To change the color of the substrate

d)

To decrease the temperature

5.

What is an antigen?

a)

A protein produced in response to stimuli

b)

A molecule that elicits antibody production

c)

An enzyme attached to an antibody

d)

A chemical that alters color

6.

What is the role of antibodies?

a)

To alter color as a result of enzyme interaction

b)

To stop the action of an enzyme

c)

To produce proteins in response to antigenic stimuli

d)

To measure color in ELISA

7.

What is an enzyme conjugate?

a)

A molecule that elicits antibody production

b)

A chemical that alters color

c)

An enzyme attached irreversibly to an antibody

d)

A process of stopping enzyme action

8.

What is a chromogen?

a)

A protein produced in response to stimuli

b)

A chemical that alters color due to enzyme interaction

c)

An enzyme attached to an antibody

d)

A process of stopping enzyme action

9.

What is the purpose of stopping in enzyme reactions?

a)

To produce antibodies

b)

To alter color

c)

To stop the action of an enzyme on a substrate

d)

To measure color in ELISA

10.

What is the function of reading in ELISA?

a)

To produce antibodies

b)

To alter color

c)

To measure color spectrophotometrically

d)

To stop enzyme action

11.

What is a microwell plate used for?

a)

To measure color in ELISA

b)

To hold samples in 8 x 12 wells

c)

To alter color due to enzyme interaction

d)

To stop enzyme action

12.

What is a multipipette used for?

a)

To measure color in ELISA

b)

To hold samples in 8 x 12 wells

c)

To dispense liquid in small-scale work

d)

To stop enzyme action

13.

Which of the following enzymes is used in ELISA?

a)

Alkaline phosphatase

b)

Amylase

c)

Lipase

d)

Trypsin

14.

What is a characteristic of a microplate washer used in ELISA?

a)

High carry-over contamination

b)

Very efficient with low carry-over contamination

c)

Manually operated

d)

Used for heating samples

15.

Which type of ELISA is based on the procedure?

a)

Direct

b)

Indirect

c)

Sandwich

d)

All of the above

16.

What is a function of a washing device in ELISA?

a)

To heat samples

b)

To manually wash samples

c)

To freeze samples

d)

To measure sample pH

17.

What type of ELISA uses a primary labeled antibody that reacts directly with the antigen?

a)

Indirect ELISA

b)

Sandwich ELISA

c)

Direct ELISA

d)

Competitive ELISA

18.

Which ELISA technique involves the use of a secondary anti-isotype antibody?

a)

Direct ELISA

b)

Indirect ELISA

c)

Sandwich ELISA

d)

Competitive ELISA

19.

In which ELISA is the antibody immobilized on a microtiter well?

a)

Direct ELISA

b)

Indirect ELISA

c)

Sandwich ELISA

d)

Competitive ELISA

20.

What is used to measure the absorbance of all wells in a 96-well plate in seconds?

a)

Enzyme-linked immunosorbent assay

b)

Spectrophotometric plate readers

c)

Microtiter plate

d)

Colorimetric assay

21.

What is the purpose of the competitive ELISA technique?

a)

To measure the amount of antigen by using a labeled antibody

b)

To measure the amount of antigen by using a sample containing antigen

c)

To measure the amount of antigen by using a substrate

d)

To measure the amount of antigen by using a microtiter well

22.

In competitive ELISA, what happens when more antigen is present in the sample?

a)

More free antibody is available to bind to the antigen-coated well

b)

Less free antibody is available to bind to the antigen-coated well

c)

The color reaction is inhibited

d)

The substrate is not added

23.

What is added after any free second antibody is removed in the Sandwich ELISA?

a)

Antigen

b)

Substrate

c)

Primary antibody

d)

Microtiter well

24.

What is the purpose of measuring absorbance at 450nm in ELISA?

a)

To determine the concentration of antibodies

b)

To detect the presence of viruses

c)

To measure the pH level

d)

To calculate the temperature