Agarose Gel Electrophoresis: Results Analysis

Lesson Transcript
Instructor: Greg Chin
Learn to analyze and interpret the results of an agarose gel electrophoresis. Explore how this lab procedure is used to analyze and troubleshoot the results of restriction digestion or a ligation step in an experiment. Updated: 08/20/2021

Purpose of Gel Electrophoresis

Gel electrophoresis is a laboratory procedure used to separate biological molecules with an electrical current. Previously, we've discussed gel electrophoresis in the context of analyzing DNA. Using an electrical current and a molecule that behaves like gelatin, called agarose, we can separate DNA molecules based on size. Although agarose gel electrophoresis can be used for a variety of purposes, two of the most common uses with respect to DNA are verifying the success of a restriction digest or a ligation step in an experiment.

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  • 0:08 Purpose of Gel Electrophoresis
  • 0:47 Analyzing a Restriction Digest
  • 2:07 Using a DNA Ladder Standard
  • 4:00 A Troubleshooting Tool
  • 5:44 Analyzing a Ligation Reaction
  • 6:43 Lesson Summary
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Analyzing a Restriction Digest

Agarose gel electrophoresis is an effective means of determining if a restriction digest procedure has been successful. Let's consider a simple example of how this works.

Often, scientists want to express a protein in a cell or tissue where it's not normally found. Suppose we want to make corn that is resistant to pest infestation, so we don't have to use so many chemical pesticides.

To do this, let's combine the DNA from two different genes, so a pest toxin can be expressed in our crop. We could accomplish this by cutting each gene with the same restriction enzyme and combining the DNA fragments to create a brand new recombinant gene. But, before any recombinant DNA can be created, we'd want to verify that the restriction digest was successfully completed.

The DNA ladder is used to determine DNA fragment size in an electrophoresis gel.
DNA Ladder Example

Let's say gene 1 is a corn gene that is 4 kilobases long, but we only want to use the first 0.5 kilobase in our new recombinant gene. And, gene 2 is a pest-resistance gene that is 3 kilobases long, but we only want to use the last 2.5 kb in the recombinant gene. In both cases, the restriction digest should replace the band in the uncut lane with two smaller bands in the digested lane.

Using a DNA Ladder Standard

Besides just concluding that one piece of DNA has been cut into two smaller DNA fragments, we can also determine the size of both the starting sample DNA and the product of a restriction digest. Recall that we can use a set of DNA molecules of known length, called a DNA ladder, to determine the size of DNA fragments in an electrophoresis gel. A DNA ladder allows us to make more precise conclusions about our gel electrophoresis results.

Notice the DNA ladder in lane one of the example below. Since we know the size of each of these bands, we can use them as a reference point for the experimental samples.

Consider lane two of the gel. By comparing the band in lane two to the DNA standards of known size, we can conclude that our initial DNA sample was in fact the correct size. Furthermore, we can also conclude that the sample did not contain any detectable nucleic acid contaminants that could disrupt future experimental steps.

Next, consider lane three of the gel. The bands in lane three represent DNA from the corn gene that has been digested with a restriction enzyme. Rather than simply conclude that the starting DNA was cut, by using the DNA ladder standards as a point of comparison, we can determine if the DNA was cut in the correct location.

Lanes four and five show the restriction digest performed on the pest-resistance gene.
Sample Gel Restriction Digest

Note that the 4 kb band in lane two has turned into two bands of 3.5 kb and 0.5 kb in lane three. Therefore, we can conclude that the restriction digest produced DNA fragments of the expected size. Additionally, it is important to note that we can also conclude that all of the starting DNA was cut because the band at 4 kb is no longer present in lane three.

A Troubleshooting Tool

We've discussed how gel electrophoresis can be used to verify that experiments have worked properly. Another major function of gel electrophoresis is to help identify the cause of a problem when something goes wrong.

Now, consider lanes four and five of our sample gel. These lanes represent the restriction digest performed on the pest-resistance gene. What size bands do we predict to see in each lane?

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Agarose Gel Electrophoresis: Results Analysis Quiz

Instructions: Choose an answer and click 'Next'. You will receive your score and answers at the end.

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A piece of DNA was digested with a single restriction enzyme. A portion of the uncut and digested DNA samples were run on the following gel. Lane 1 represents the DNA ladder. Lane 2 represents the uncut DNA sample. And, lane 3 represents the product of the restriction digest. Which of the following statements explains the results?

I. Loading buffer was not added to the DNA samples.

II. The gel was not stained with ethidium bromide.

III. The scientist accidentally used water instead of DNA in lanes 2 and 3.

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