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MBT ELISA & Antibodies

Total questions: 20

Worksheet time: 11mins

Name
Class
Date
1.

What term describes a molecule on a pathogen to which an antibody can bind?

(a)  

2.

Antibody structure is commonly

a)

Z shaped

b)

Y shaped

c)

W shaped

d)

T shaped

3.
Antibodies not only protect us from infections, they can also be used in laboratories to determine whether or not a patient has or has had a disease.
a)
TRUE
b)
FALSE
4.
Why is it necessary to wash the samples repeatedly?
a)
it is important to keep the lab wells clean
b)
it is important to wash away all bound and unbound antibodies from teh wells
c)
it is important to wash away the unbound antibodies
d)
washing the wells is just solid lab practice
5.
Why is a positive and negative control necessary in the setup of ELISA?
a)
positive controls are equal to negative controls 
b)
ELISA is subject to errors; if controls fail the results are untrustworthy
c)
ELISA is a well run test that typically does not need controls
d)
negative and positive controls are needed to exclude all results
6.

When a positive + result occurs in an ELISA test, then one could conclude that...

a)

a + result always means illness

b)

the antibody is present

c)

it is a false + and no illness

d)

an enzyme is present

7.
What is another name for antibodies (Ab)?
a)
helper t cells
b)
hemoglobin
c)
immunoglynocists
d)
immunoglobulins
8.

During an ELISA lab, you prepare a set of dilutions...why?

a)
serial dilutions help determine the level of Ab present in a sample
b)
serial dilutions identify the pathogen
c)
serial dilutions help determine the level of macrophages present
d)
serial dilutions identify the killer T cells present
9.

What is a primary antibody?

a)

Patient's antibody and initial step in ELISA

b)

Antibody with bound enzyme

c)

The most important antibody

d)

a chicken antibody

10.

The immune system of human may respond to the epitopes on the surface of an invading organism by

a)

Inhibiting the action of B cells

b)

Disrupting the mitochondria of the invading organism

c)

Producing antibodies

d)

Altering the DNA sequence of the invading organisms

11.

Antibodies consist of

a)

A light chain and 2 heavy chains

b)

2 light chains and 2 heavy chains

c)

2 light chains and a heavy chain

d)

All options are true because there are many types of antibodies

12.

The part of an antigen molecule to which an antibody attaches itself is called a(n)

(a)  

13.

What kind of antibody isotope can pass from mother to fetus?

a)

IgM

b)

IgG

c)

IgA

d)

IgD

14.

In an ELISA test, what does the secondary antibody recognize?

a)

The antigen

b)

The antibody

c)

The antigen-antibody complex

15.

Why is a colorless substrate added after the final washing step of an ELISA lab?

a)

To remove any unbound antibodies

b)

To cause a color change

c)

To wash the well

d)

To indicate the presence of the primary antibody

16.

Which of the following cannot be determined by an ELISA test?

a)

Concentration of antigens

b)

Presence of pathogen

c)

Genetic sequence of a pathogen

d)

Presence of protein

17.

What are Monoclonal antibodies ?

a)

An antibody produced by the body.

b)

An antibody produced by a single clone of cells or cell line and consisting of identical antibody molecules.

c)

An antibody produced by a single clone of cells or cell line and consisting of many different antibody molecules.

d)

An antibody produced in a lab

18.

Monoclonal antibodies can be used for...

a)

Cancer treatment

b)

Pregnancy detection

c)

Tissue transplants

d)

Autoimmune disorders

19.

5.) In what order should you add the reagents to perform an indirect ELISA test?

a)

a.) Primary antibody, antigen sample, enzyme-linked secondary antibody, substrate

b)

b.) Antigen sample, primary antibody, enzyme-linked secondary antibody, substrate

c)

c.) Substrate, enzyme-linked secondary antibody, antigen samples

d)

d.) Primary antibody, enzyme-linked secondary antibody, antigen samples, substrate

20.

Put the steps of an ELISA assay in order.

a)

make serial dilutions of antigen of interest for comparison

b)

add samples to be tested

c)

add primary Ab to all wells, let develop then wash

d)

add secondary Ab with attached enzyme to all wells, develop and then wash

e)

add substrate to all wells

1)
2)
3)
4)
5)