1123581321 Posted April 30, 2011 Share Posted April 30, 2011 Hi, i'm wondering if this is correct for primers and sequencing etc. its just what i've gathered from trying to understand it.. So is it that DNA strands will respond to the primer of another if its compatible, whereby the complementary base pairs are pieced together since recognition is apparent in both strands.. kind of like piecing a jigsaw together whereby even if there are missing pieces, in general the details will be able to be placed in or connected because they are unique to their localities of the puzzle..., therefore in DNA, the nucleotides are specific to their strands and can therefore replace missing links for a complete sequence, even if they are missing, because they still recognise the specific genetic code... Link to comment Share on other sites More sharing options...
Horza2002 Posted May 1, 2011 Share Posted May 1, 2011 Is this so that you can do PCR on your sample? If so, then the primer that you have, are about 20 base pairs complimentary to the 3' and 5' end of the DNA strand. So once you have added your primers to the DNA sample, it will anneal to each end which provides a "handle" for DNA polymerase to bind and replicate the DNA strand. Is that ok? Link to comment Share on other sites More sharing options...
1123581321 Posted May 1, 2011 Author Share Posted May 1, 2011 sorry i probably should of been more specific. im not doing any experiment or anything, i was simply asking if what i said about the sequencing is correct, just for knowledge sake... while im on the matter, why are the ends of DNA called 3' & 5' and 2 or whatever ? Link to comment Share on other sites More sharing options...
hypervalent_iodine Posted May 2, 2011 Share Posted May 2, 2011 It's to do with the position of functional groups on the deoxyribose. The terminal hydroxy is at the 3' position, which means that it is on the 3' position on the ring. The starting phosphate is similarly on the 5' position on the ring. It's just the numbering convention. Link to comment Share on other sites More sharing options...
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