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I have designed primers for pcr of blood dna, but the problem is the primers are showing multiple bands after doing pcr. These are self designed primers. Why is this problem occurring?
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I have done 285 samples of human blood DNA extraction, and measured the DNA Concentration and A260/280 and A260/230 in a nano drop machine. This is done before PCR. Now the values of A260/230 are...
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