
DNA Technology
Quiz
•
Biology
•
10th Grade
•
Easy

Timara Tia Gabas
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15 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What does the term PCr stand for?
Polymerase Chain Reaction
Preliminary Chain Reaction
Polymerase Coiled Reaction
Protein Chain Reaction
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Explain the process of gel electrophoresis.
Gel electrophoresis separates RNA fragments based on their size and charge by running them through a liquid matrix using an electric field.
Gel electrophoresis separates DNA fragments based on their color and texture by running them through a gel matrix using an electric field.
Gel electrophoresis separates DNA fragments based on their size and charge by running them through a gel matrix using an electric field.
Gel electrophoresis separates proteins based on their shape and weight by running them through a gel matrix using a magnetic field.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How is recombinant DNA technology used in medicine?
To improve crop yield through genetic modification
To produce therapeutic proteins through genetic engineering
To create new species of animals
To develop new types of antibiotics
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the significance of DNA fingerprinting in forensic science?
It helps in identifying individuals, solving crimes, and exonerating the innocent.
It is not a reliable method for identifying individuals
It is only used for entertainment purposes
It has no significance in forensic science
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is gene cloning?
Mixing different genes together
Creating multiple copies of a gene or DNA sequence.
Using a microscope to view genes
Deleting a gene from the DNA sequence
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What are the three main steps of PCR?
Cutting, Pasting, Copying
Denaturation, Annealing, Extension
Heating, Cooling, Reading
Mixing, Separation, Amplification
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How does gel electrophoresis separate DNA fragments?
By using a magnetic field to separate the DNA fragments
By heating the gel to separate the DNA fragments
By adding chemicals to the gel to separate the DNA fragments
By applying an electric field to the gel, causing the DNA fragments to move towards the positive electrode at different rates based on their size and charge.
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