In our current project, we're working with the Rapid SARS-CoV-2 Antigen Test Card and have incorporated polyethylene glycol (PEG-3350) at a concentration of 68 mg/mL into the running buffer. Unexpectedly, we've observed a significantly brighter test line even when no antigen is present in the sample—only the processing solution and PEG-3350 are included.
We suspect this phenomenon may be due to non-specific binding or interactions between PEG-3350 and components of the assay.
Has anyone encountered similar effects when using PEG-3350 in lateral flow assays? What strategies or modifications have you found effective in mitigating such non-specific signals?
Any insights or suggestions would be greatly appreciated.