00:01
So i have explained pcr in a previous video, but let's take it from the top one more time.
00:06
So we have our original dna with the sequence we're interested in lying somewhere around here.
00:16
What happens is we raise the temperature, so the two strands, the double strand, the molecule is denaturated, so we get two single strands.
00:27
And then we add primers to the mix and lower the, temperature so the primers hybridized with the sequence we want so these are our primers we do make our own primers now so that's not a problem and then we add a polymerase that is resistant to heat we take it from some bacteria that live in hot springs and what happens is the the primers are elongated and they the sequence is created and then we have of course hydrogen bonds forming here and here and we have doubled the amount of sequence of the the number of the time we have the sequence that we were interested in and this happens again and again and again in cycles which are automated of course and the number of times we have the sequence we're interested in is it grows exponentially and this is what pcr is all about.
01:34
Now, it does not use rna polymerase, so statement a doesn't make sense.
01:40
It uses dna polymerase.
01:42
It doesn't take place in huge bioreactors.
01:44
It's actually quite compact, the place where this happens.
01:50
It does use dna replication in vitro...