Choose from solid polystyrene plates in a standard 96-well format or polystyrene modules consisting of twelve 8-well strips

All of the plates utilize spacer arm chemistry to covalently couple the affinity capture surface molecules. The glutathione plates are ideal for rapid coupling of GST-tagged fusion proteins. Nickel-chelate plates are ideal for rapid coupling of 6xHistidine-tagged proteins. Streptavidin plates are ideal for binding of biotinylated biomolecules such as peptides, antibodies, nucleic acids, or haptens and have an excellent binding capacity of 20pmol/mL.

Choose from solid polystyrene plates in a standard 96-well format or polystyrene modules consisting of twelve 8-well strips

All of the plates utilize spacer arm chemistry to covalently couple the affinity capture surface molecules. The glutathione plates are ideal for rapid coupling of GST-tagged fusion proteins. Nickel-chelate plates are ideal for rapid coupling of 6xHistidine-tagged proteins. Streptavidin plates are ideal for binding of biotinylated biomolecules such as peptides, antibodies, nucleic acids, or haptens and have an excellent binding capacity of 20pmol/mL.

All of the plates utilize spacer arm chemistry to covalently couple the affinity capture surface molecules. The glutathione plates are ideal for rapid coupling of GST-tagged fusion proteins. Nickel-chelate plates are ideal for rapid coupling of 6xHistidine-tagged proteins. Streptavidin plates are ideal for binding of biotinylated biomolecules such as peptides, antibodies, nucleic acids, or haptens and have an excellent binding capacity of 20pmol/mL.

Choose clear plates and strips for colorimetric assays, white plates for bioluminescence and chemiluminescence assays, and black plates for fluorescence assays. Certified clear plates guarantee uniform well-to-well binding capacity of CV ≤5%; certified black and white plates guarantee uniform well-to-well binding capacity of CV ≤7.5%.

LockWell™ modules feature 8-well break apart strips that can be separated into individual wells and then locked into a frame at the same horizontal level for uniform washing and reading. Plates have a high signal-to-noise ratio, no surface leaching, minimal steric hindrance of bound molecules, and highly reproducible binding with low CVs. They require no blocking or activation steps and feature highly specific binding. Plates are also stable for long periods at room temperature.