A quick question which I just want to see that I understand right
So first aid states that in PCR you add premade DNA primers specific for the sequence to be amplified.
I always understood this to mean that if you're looking for an ATCG region, you're going to put in DNA primers specific/complementary to that. And if it works that means hey that region exists in there
But from my reading of a UWSA question explanation, it looks like you actually put in the "flanking DNA primers" ie the region next to it?? This is in bold and actually makes less sense to me
How do you know what primers to give in that case? Do we know the flanking regions for every sequence of interest? And are they always the same?
So first aid states that in PCR you add premade DNA primers specific for the sequence to be amplified.
I always understood this to mean that if you're looking for an ATCG region, you're going to put in DNA primers specific/complementary to that. And if it works that means hey that region exists in there
But from my reading of a UWSA question explanation, it looks like you actually put in the "flanking DNA primers" ie the region next to it?? This is in bold and actually makes less sense to me
How do you know what primers to give in that case? Do we know the flanking regions for every sequence of interest? And are they always the same?