I am trying to do RAPD PCR with Promega green master mix with parameters 95 : 5min , 95 : 1min, 38 : 1min , 72: 2min with 35 cycles but not getting a very distinct band pattern on 2% GEL. what could be the possible reason for that.
I would make sure that the gel was completely set and cool before loading . Load less pcr product and run the gell at2/3 the voltage that you used on the pictured gel