7) When running a gel electrophoresis, should we place the DNA sample towards the positive or the negative end? Why? 8)
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7) When running a gel electrophoresis, should we place the DNA sample towards the positive or the negative end? Why? 8)
7) When running a gel electrophoresis, should we place the DNA sample towards the positive or the negative end? Why? 8) What would happen if we chose the wrong primers to perform our PCR?
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