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That stain and exposes the dna molecules and hopefully i can isolate that molecule and wash away the debris and chemicals in that sample. the next step is calmed quantification, i take that sample and see how concentrated, how much dna was i able to recover from that stay in. i use that for the next step called amplification. i m basically makeing xerox copies almost of the dna molecule but only at 13 or 15 different regions i m interested in testing to develop the dna profile. i make millions and millions of copies of the molecule at these specific regions so i can analyze these regions. the last step is called electrophoresis, where i actually separate out the dna molecules i was able to amplify by size. i get a data readout, i interpret that, and create dna profile, a set of interpret. i can use those numbers for ....