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? 

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