Detection Methods

Assay kitsFoundational

The choice of signal chemistry determines your achievable sensitivity, required instrumentation, and sample compatibility. Understanding these trade-offs before selecting a kit saves costly optimization steps.

4
Detection chemistries
8
Decision attributes
fM – mM
LOD range covered
Assay kit detection chemistry — selecting your signal modality
Attribute Colorimetric Fluorometric Chemiluminescent ELISA-based
Detection principle Absorbance (visible light) Fluorescence emission Light emission (enzymatic / oxidative) Enzyme-linked antibody signal
Sensitivity (LOD) µM – mM range nM – pM range fM – aM range pg/mL – ng/mL
Instrument required Plate reader (340–750 nm) Fluorescence plate reader Luminometer or enhanced plate reader Plate reader (450 nm standard)
Background interference Moderate (colored samples) Moderate (autofluorescence) Low Low
Dynamic range
Multiplexing Not standard Possible (wavelength mux) Limited With bead arrays
Sample compatibility Cell lysates, purified fractions, clear supernatants Cell lysates, live cells, serum Serum, plasma, cell supernatant Serum, plasma, urine, tissue homogenate
Best for Metabolites, enzyme activity, protein concentration (BCA/Bradford) Oxidative stress, apoptosis, kinase activity, cell viability Reporter assays, low-abundance biomarkers, ultra-sensitive detection Validated biomarker quantification, clinical research samples

LOD = limit of detection. Absolute values are kit- and target-dependent — refer to individual CoAs.