I have followed the kit instruction, however, after I added the elution buffer to both of the 2 samples (from the same stem of the plant) for DNA extraction, I find out one of the AC column contains more liquid than the other one, so I pipette the excessive liquid from one AC column (for one sample) to another one (for another sample). It seems to be not a good idea, but does it mean that the two samples cannot be used?
In another DNA extraction, I added the elution buffer not to the centre of the AC column (suggested by the instruction in the kit), does it mean that I better discard these samples?
I only tried DNA extraction for three times... so...
Wish someone could help... Thanks!