I used Ubiquitin 5 as control primer to check balance cDNA and I got a good result. But when I tried to check with another control primer like Ubiquitin 1 or OsActin, those bands were different (if among 3 control primers, we can get 2 in the same result, and then go to next step). What should I do now? Should I try to find better control primers or should I try to get balance from Ubiquitin 1 result?