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When the samples have run far enough down
the gel to provide a good separation, a picture is taken of
the gel by placing it on a lightbox. As you can see, the
areas on the gel where the DNA has migrated light up,
showing the pattern of the sample. Now the DNA is
transferred from the gel to a nylon support, like this white
membrane, and crosslinked to hold the DNA in place. Before
the transfer, the DNA is denatured in the gel to separate
the stands of the double helix.
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