I'm doing Surface Plasmon Resonance for a series of samples with different concentration starting with lowest concentration. Binding is so strong that I cannot reach the baseline after washing step with running buffer. Each time just part of binding dissociate. And then I test the next concentration. Several regeneration solutions have been tested but nothing could bring the signal to the baseline.

I use a Reichert SPR device and use Scrubber for analyzing the data.

How can I interpret these data in Scrubber, without a complete dissociation and/or regeneration?

Any thought would be highly appreciated.

Similar questions and discussions