DNA-linked competitive probes address weak sensitivity in hormone assays by combining ligand binding, modular linkers, and detectable tags.
Overlapping fluorophore spectra complicate particle sorting; generalized least squares estimates abundances for more precise identification.
Current protein methods miss single-molecule sensitivity or spatial context; reactive groups tether N-terminal amino acids for high-throughput sequencing.
Aldehyde-scavenging agents reverse masking in fixed tissue, restoring antigen access for immunostaining while preserving morphology.