After reading Abs260 of only 2uL of my DNA samples using this uDropPlate I have calculated the DNA concentration following the protocol's equation :
DNA concentration(ug/ml)= Abs260 X 50(ug/ml) X multiplication factor (10mm/0.5mm)
I found that the resulted concentrations are very high and I am significantly overestimating my DNA concentrations.
What is the right calculation to get DNA concentration in my case?