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Gel Electrophoresis Concepts and Techniques

Gel Electrophoresis Concepts and Techniques

Assessment

Interactive Video

Biology, Chemistry, Science

9th - 12th Grade

Practice Problem

Hard

Created by

Patricia Brown

FREE Resource

The video tutorial explains gel electrophoresis, a method for separating DNA by size using an electrical field. It covers preparing agarose gel, loading samples, and running the gel. Tips for achieving clear DNA bands and safety precautions are provided. The video concludes with a call to explore more resources.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary purpose of gel electrophoresis?

To separate DNA by size

To amplify DNA

To clone DNA

To sequence DNA

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What determines the size of pores in an agarose gel?

The concentration of agarose

The temperature of the gel

The voltage applied

The type of buffer used

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is TBE buffer preferred for longer electrophoresis runs?

It is easier to prepare

It provides better DNA separation

It is less prone to overheating

It is cheaper than TAE

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What safety precautions should be taken when handling ethidium bromide?

Use a fume hood

Wear a lab coat, eye protection, and gloves

Work in a dark room

Use a face mask

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the purpose of adding a DNA ladder to the gel?

To prevent the gel from melting

To determine the length of DNA fragments

To help visualize the gel

To increase the voltage

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the recommended voltage range for running most gels?

50-100 volts

80-150 volts

150-200 volts

200-250 volts

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a potential risk of running the gel at too high a voltage?

The gel may melt

The DNA may degrade

The bands may not separate

The buffer may evaporate

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