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You’re trying to PCR amplify a gene, but your gel shows that there are two bands...

You’re trying to PCR amplify a gene, but your gel shows that there are two bands instead of only one like you expected. You know for certain that there no homologous genes in the genome from which you’re amplifying, so you assume that the issue must be coming from your primers or PCR conditions. Briefly describe 2 different strategies for solving the problem and how they work.

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Answer #1

One strategy to solve the problem is that,the annealing temparature might be too low.At low temperatures the primers starts hybridising. So increasing the annealing temperature can solve the problem.

Other strategy is that,the DNA concentration might be too low. If more primers are used, the DNA concentration will be varying at diferent sites. This problem can be solved by using a better template concentration

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