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Why can gel electrophoresis separate dna fragments?

Updated: 8/9/2023
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Anthony King Jr

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4y ago

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The markers are of a specific size (in numbers of base pairs). By comparing the rates of migration of the various markers with the rates of migration of the gene/genes you are separating, you can get an estimate of the size of the fragments you are interested in. They also let you know if you need more or less separation. If the smaller fragments run off of the gel, you'll know that you need to run if for a shorter time or with a smaller voltage.

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14y ago
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14y ago

The bands shown in the marker are of known size (for example a DNA fragment). Compare your sample with the marker, and you know the size of your sample DNA fragment. If you have estimated the size of the DNA fragment before (with software, like clone manager), you can check whether the fragment in your sample is the one you want.

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Muscle Pig

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3y ago

DNA fragments are negatively charged, :: Apex

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13y ago

DNA fragments of different sizes appear as different bands or lines on a gel

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Q: Why can gel electrophoresis separate dna fragments?
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What is used to separate DNA fragments by size?

Electrophoresis. Restriction enzymes are used to cut DNA into fragments. Solutions containing these fragments are placed on the surface of a gel to which an electric current is applied. The electric current causes the DNA fragments to move through the gel. Because smaller fragments move more quickly than larger ones, this process separates the fragments according to size.


Are restriction enzymes used in gel electrophoresis?

For DNA gel electrophoresis, yes. Once the DNA is cut up into different-sized fragments, they can be electrophoresed to separate bands.


What procedure is used to separate and analyze DNA fragments by placing a mixture of DNA fragments at one end of a porous gel and supplying an electrical voltage to the gel?

agarose gel electrophoresis


DNA fragments can be separated and analyzed by?

Pulse field gel electrophoresis is used to separate DNA fragments by their size.


Where do you get the DNA fragments for Gel electrophoresis?

The DNA fragments comes from the method of DNA isolation.


How are DNA fragments separated on DNA fingerprinting?

Gel electrophoresis


Gel electrophorysis and GMO food?

Gel electrophoresis is a method for separation and analysis of macromolecules (DNA, RNA and proteins) and their fragments, based on their size and charge.The tool of DNA gel electrophoresis was developed in the 1970s. The process uses electricity to separate DNA fragments by size as they migrate through a gel matrix.It can be used to separate proteins that are used in genetically modified foods.


What is a technique for sorting DNA fragments by length?

it is called " electrophoresis"


Process that restriction fragments of DNA are separated from each other by the use of electricity?

The process is referred to as gel electrophoresis. This is an analytical process where DNA fragments can be separated based on size within a gel under the influence of an electric field


What explains the role of gel electrophoresis in forensic science?

It is a special technique used to separate and identify DNA fragments.


How does DNA and gel electrophoresis relate?

Gel electrophoresis separates an individual's DNA fragments from one another according to size. An electric current repels a mixture of the negatively-charged DNA fragments through microscopic pores in the gel from the negative to the positive electrode. Upon completion, the separated fragments of DNA can be visualized as a ladder of small bands in the gel by staining with a methylene blue dye solution or smaller DNA segments move more easily through the gel.


Explain how an agarose gel can separate DNA fragments of different lengths.?

The separation of DNA fragments is based on size. When a DNA sample is run in a gel (electrophoresis), the lighter fragments migrate faster than the heavier (longer) fragments under the influence of an electric current. At the and of the process, the shorter fragments are found at the terminal end of the gel and the longer fragments closer to the origin