Hello,
Today i want to ask about ratio of developer and fixer in western blot.
According to instruction, the dilution ratio of developer and fixer is both
1:4(for example, 200ml developer or fixer and 800ml water)
But i recognized that ratio can be different than 1:4 due to my error
during dilution. But I have found no problem considering my detection results in western blot.
So I concluded that the error in dilution ratio is just minute
and is not critical in my detection results.
But it is just my conclusion so I want to get more objective feedback
from others. Thank you!