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I didn't design my primers that produce A overhang. And I have to do cloning. I read that I can use dATP and nonproofreading Taq to produce A overhang. Can I use this method to add an A to my PCR...
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We isolated DNA from FFPE by manuel method. We done PCR but in gel there are some smear and we dont know how can we solve this problem. Can anyone have a solution?And why saw smear in PCR?
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