Why is it important to amplify the gene of interest before introducing recombinant DNA into a host cell?

PCR Techniques and DNA Amplification

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Biology, Science, Chemistry
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9th - 10th Grade
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Hard

Patricia Brown
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10 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
To ensure the gene is not lost during the process
To create multiple copies for better analysis
To change the gene's sequence for better results
To make the gene resistant to host cell enzymes
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the main advantage of the PCR technique?
It requires living organisms to function
It can be performed in a laboratory without living organisms
It is dependent on bacterial enzymes
It was developed in the 1990s
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Who developed the PCR technique and when?
Carrie Mulus in 1983
James Watson in 1953
Rosalind Franklin in 1951
Francis Crick in 1962
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the role of a DNA template in PCR?
To change the DNA sequence
To inhibit unwanted reactions
To provide a sequence for amplification
To act as a catalyst
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which enzyme is crucial for creating new DNA strands in PCR?
Helicase
RNA polymerase
Ligase
DNA polymerase
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How does DNA polymerase contribute to DNA strand creation?
By joining two DNA strands together
By removing incorrect nucleotides
By adding complementary nucleotides to a template strand
By breaking down nucleotides
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the primary function of DNA polymerase in PCR?
To cut DNA strands
To add nucleotides to the primer
To unwind the DNA helix
To bind DNA strands together
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