Signal Enhancer BAP-1: Core Functions and Application MechanismsCore Functions
Signal enhancer BAP-1 possesses a unique molecular structure that grants it multifunctional performance in immunodiagnostics. Its core functions primarily include: preventing particle aggregation, enhancing reagent compatibility, improving luminescence efficiency, protecting enzyme activity, reducing non-specific adsorption, and inhibiting spontaneous oxidation .Core Application Scenarios and Mechanisms of Action
1. Dispersion and Stabilization of Nanomarkers
Mechanism of Action:
Signal enhancer BAP-1 adsorbs onto the surface of nanomaterials (such as colloidal gold, quantum dots, magnetic microspheres, latex microspheres) through its hydrophobic chains, while the hydrophilic chains form a steric hindrance, preventing aggregation and improving the dispersion and long-term stability of markers in reagents .
Typical Applications:
Immunochromatographic strips: Stabilization of quantum dot-labeled antibodies (0.1%–0.3% signal enhancer BAP-1) to avoid particle aggregation after the conjugate pad dries.
Chemiluminescent reagents: Uniform dispersion of magnetic microspheres (0.05%–0.2% signal enhancer BAP-1), reducing batch-to-batch variation.
Immunoturbidimetric reagents: 0.05-0.2% Tetronic 1307 + 0.1% signal enhancer BAP-1 to disperse chylomicrons in lipemic samples.
Dosage Range: 0.05%–0.5% (w/v), adjustment required based on the surface charge and hydrophobicity of the nanomaterials .
2. Reduction of Non-Specific Adsorption (Blocking Agent)
Mechanism of Action:
Signal enhancer BAP-1 adsorbs onto hydrophobic areas of solid-phase carriers (such as nitrocellulose membranes, microplates, electrodes), forming a hydrophilic barrier that blocks the non-specific binding of impurity proteins or lipids from the sample, thereby reducing background signal .
Typical Applications:
Lateral flow strips: Sample pad pretreatment (0.1%–0.3% signal enhancer BAP-1 + 0.02%–0.1% (w/v) Tetronic 1307) to reduce interference from fibrin in blood.
Microplate ELISA: Replacing traditional BSA blocking solutions (0.2%–0.5% signal enhancer BAP-1), reducing costs by 30% and providing more durable blocking effects.
Dosage Range: 0.1%–0.5% (w/v), excessively high concentrations may affect target molecule binding .
3. Enhancement of Detection Sensitivity (Micellar Sensitization)
Mechanism of Action:
The micelles formed by signal enhancer BAP-1 can concentrate luminescent substrates (e.g., luminol), fluorescent dyes, or enzymes (HRP, ALP), increasing the local reaction concentration and enhancing signal intensity .
Typical Applications:
Chemiluminescent Immunoassay (CLIA): Adding 0.05%–0.1% signal enhancer BAP-1 to the luminol system can increase signal strength by 20%–50%.
Fluorescent PCR: Adding 0.01%–0.05% signal enhancer BAP-1 to the probe system reduces probe adsorption and improves Ct value consistency.
Lateral Flow Strips: 0.1%–0.3% signal enhancer BAP-1 + 0.02%–0.1% (w/v) Tetronic 1307 to enhance the binding probability with detection line antibodies.
Dosage Range: 0.01%–0.1% (w/v), excessive amounts may inhibit enzyme activity or cause over-encapsulation by micelles .
4. Lyophilization Protection
Mechanism of Action:
Acts as a lyoprotectant to reduce denaturation during the freeze-drying and reconstitution process .
Enzymes/Antibodies: 1%–5% signal enhancer BAP-1 + trehalose.
Nanoparticles: 5%–10% signal enhancer BAP-1 + polyols.
Liposomes: 8%–15% signal enhancer BAP-1 + chelating agents.
Typical Application:
Lyophilized Chemiluminescent Microspheres: 10% signal enhancer BAP-1 + 5% trehalose, achieving a dispersion efficiency >95% after reconstitution .
5. Solubilization of Hydrophobic Components
Mechanism of Action:
Micelles encapsulate hydrophobic molecules (e.g., certain fluorescent dyes, fat-soluble antigens), improving their solubility in aqueous reagents .
Typical Applications:
Fluorescent Microsphere Labeling: Addition of 0.5%–1% signal enhancer BAP-1 when dissolving hydrophobic dyes (e.g., Nile Red).
Lipid Antigen Extraction: 0.3% signal enhancer BAP-1 in sample processing solution improves lipoprotein antigen recovery rate .