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The Human Genome Project



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Gel Electrophoresis

Slide 15

March 2009

They are then added to a gel electrophoresis apparatus where you put a little bit of buffer on the top, a little bit on the bottom. You attach electrodes so that the positive electrode is towards the bottom. Since the DNA is negatively charged, it will be attracted to the positive electrode and the various DNA fragments that have synthesized will be migrating through the gel. And the only thing is that the fragments are able to traverse the gel more quickly than the larger fragments so that one can see the single base at the very bottom of the gel 2, 3, 4, etc. all the way up the gel and then one simply looks at where one is along the gel and one can determine the length of the growing chain. When this is done, you simply open the gel up.

Gel Electrophoresis

 


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