I have been reading many papers but struggling to find a clear explanation for how to interpret the data apart from lower FP - faster tumbling, higher FP slower tumbling. I've not been taught on this topic, but have been given data to analyse as part of my honours project.
The data is on florescence polarisation with heparin, I also have random spikes in data, where FP is reading low at a certain concentration of heparin but one replicate will read a very high FP from the rest of the replicates in that concentration, is there an explanation for this?
Any help would be greatly appreciated. Thankyou.