Select your candidates with confidence: - Sensitivity and high-quality binding data enable better-informed decisions
Avoid data evaluation bottlenecks: - Innovative software solutions for improved productivity: evaluate up to 4800 interactions in less than 2 hrs
Integrate into your workflow: - Advanced LIMS integration support and convenient data export for customized analyses
Seamless transition into regulated environments: - Validated software facilitates 21 CFR Part 11 compliance
Screening and ranking of antibodies and antibody fragments direct from crude supernatants or lysates - yes/no binding, selectivity
Detailed characterization of antibodies and antibody fragments - specificity/selectivity as well as isotyping kinetics, affinity, concentration
LMW drug discovery
Screening of LMW compounds (incuding fragments) - direct binding analysis, selectivity & stoichiometry
Compound characterization from hit validation to lead optimization - binding selectivity, affinity & kinetics
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