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In the enzyme-linked immunosorbent assay, antigens, antibodies and other biomolecules are adsorbed to the surface of the carrier through a variety of mechanisms, including passive adsorption through hydrophobic bonds, water/ionic bonds, and the introduction of other active groups such as amino and The covalent bonding of carbon groups and the bonding through hydrophilic bonds after?surface modification. The Elisa plate is mainly divided into detachable and non-detachable. Among them, the transparent plate is suitable for quantitative and qualitative solid-phase immunodetection and binding detection; the black plate is suitable for fluorescence immunoassay and binding detection; the white plate is suitable for self-luminescence and chemiluminescence; and is suitable for most?standard equipment.
The protein adsorption capacity of the ELISA plate is divided into three levels: Low binding capacity: preferentially bind to molecules containing significant hydrophobic regions (lipids, lipoproteins, large proteins)
Medium binding capacity: binding to biomolecules with hydrophilic/hydrophobic properties (medium and large protein, immunoglobulin, albumin)
High binding capacity: preferentially bind biomolecules with hydrophilic/hydrophobic properties (small to large proteins, immunoglobulins, albumin, LPS, proteins)
Features
*Size conforms to SBS international standard;
* Good uniformity between wells to ensure the accuracy of ELISA experiments;
*Excellent well inner surface treatment technology to improve protein binding ability;
*Numbers and letters are auxiliary identification, which is convenient for the identification of samples in different wells;
*Transparent, white, and black are available to meet various experimental requirements.
