What problem arises when you have multiple DNA bands after PCR amplification?
Biotechniques | Principles of Gel Extraction

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Science, Biology
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University
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Hard
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7 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
It causes issues with sequencing and cloning.
It leads to a pure DNA sample.
It enhances the expression of proteins.
It simplifies the cloning process.
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is gel extraction necessary when dealing with multiple DNA bands?
To avoid using an expression vector.
To mix different DNA sequences.
To isolate and purify the desired DNA band.
To increase the number of DNA bands.
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the purpose of making a thicker gel for gel extraction?
To decrease the electrophoresis time.
To make the gel easier to handle.
To allow for more DNA to be added and separated.
To reduce the amount of DNA used.
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the role of electrophoresis in gel extraction?
To reduce the DNA concentration.
To increase the thickness of the gel.
To separate DNA bands based on size.
To combine different DNA bands.
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which tool is mentioned as efficient for cutting out DNA bands from the gel?
A microscope
A gel extractor tip
A pair of scissors
A scalpel
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is a key advantage of using gel extractor tips?
They are used for mixing DNA.
They are made of metal.
They are sterile and disposable.
They are reusable.
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the final step after extracting the desired DNA band using a gel extraction kit?
Discarding the DNA sample.
Sending it for sequencing.
Mixing it with other DNA bands.
Storing it in a freezer.
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