I have a problem with detection of cDNA synthesis where when I put it on the gel , there were any smears so what the meaning of that and what can I do?
first , the amount of cDNA is 1371 ng/1ul so I think that reason is not really for my case, however it may contamination with DNase , so I will prepare new one
Bur regarding your recommendation to running Pcr by specific primers , I read that it is better to detect by housekeeping genes so , what is your recommendation