Hey everyone,
I ran the Real-Time ATP Rate Assay Kit on an XFe24 -- multiple plates were used to run all sample. Each plate consisted of the 4 background wells, 4 experimental samples (quadruplicate), and a control sample (quadruplicate, same sample on each plate). Statistical analysis found there was no significant difference between plates for my control. What is the best method to account for inter-plate variation? Does Agilent have a standard method to account for this?