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Mol Bio Quiz4

Total questions: 6

Worksheet time: 5mins

Name
Class
Date
1.

What is the correct sequence of steps involved in nucleic acid isolation?

a)

Nucleic acid precipitation -> Removal of cell debris -> Lysis -> Dissolving nucleic acid -> Protein digestion

b)

Lysis-> Removal of cell debris -> Nucleic acid precipitation -> Protein digestion -> Dissolving nucleic acid

c)

Lysis -> Protein digestion -> Removal of cell debris -> Nucleic acid precipitation -> Dissolving nucleic acid

d)

Lysis -> Removal of cell debris -> Protein digestion -> Dissolving DNA -> Nucleic acid precipitation

2.

In a real-time PCR reaction, linear (TaqMan) probes generate signal when cleaved due the 5' to 3' exonuclease activity of DNA extension polymerase and molecular beacons generate signal when they bind to their complementary sequence. In which step of the PCR cycling will you keep the camera on to detect nucleic acid amplification?

a)

TaqMan probes: Initial extension

Molecular beacons: Final extension

b)

TaqMan probes: Denaturation

Molecular beacons: Annealing

c)

TaqMan probes: Extension

Molecular beacons: Annealing

d)

TaqMan probes: Extension

Molecular beacons: Extension

3.

You are to design a PCR assay to test for COVID. List all the enzymes you will need for the assay.



4 lines
4.

Which of the following techniques can be used to visualize genomic DNA which is 200kb long, using lab equipment you have used in this semester?

a)

Using DNA probes and measuring fluoresence

b)

Gel electrophoresis

c)

SDS PAGE

d)

Pulsed field gel electrophoresis

5.

The sequence of a target gene you are testing for is given below:

5'GGTAGCTTAGCTGACTGCCATGGCATG........GGTCGATCGTTAACTGGATCCGGATGCAT3'

The sequence mapped for primer design is highlighted in red. Write the correct sequence for the primer set in 5' to 3' direction.

a)

AATCGACTGACGGT

AND

AATTGACCTAGGCCTA

b)

TGGCAGTCAGCTAA

AND

AATTGACCTAGGCCTA

c)

TTAGCTGACTGCCA

AND

ATCCGGATCCAGTTAA

d)

ACCGTCAGTCGATT

AND

ATCCGGATCCAGTTAA

6.

Match the following

a)

60-65 Deg C

1.

LAMP

b)

Thermal cycling

2.

PCR

c)

60-64 Deg C

3.

HDA

d)

35-37 Deg C

4.

RPA