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Universally applicable, selma streamlines high-throughput screening by capturing antibodies in their natural form, allowing for early characterization and direct production without recloning. Flexible and efficient, it enables selection from 1 million antibody-producing cells per screening.
Camelid nanobodies are only one-tenth the size of a conventional antibody (12-15 kDa versus 150 kDa), making them the smallest antigen-binding moiety found in nature. Based on their single antigen binding site, they can adopt a specific finger-like structure to recognize and bind hidden or buried target epitopes.
These properties can be translated into novel forms of antibody-based diagnostic products and drug therapies.
We base our immunization strategy onto the most efficient danger signals to the mammalian immune system: viruses. By combining efficient surface-related epitopes with a viral particle system originated from the hamster polyomavirus, we are able to perform a hyper-immunization schedule, extraordinarily faster than conventional immunization strategies. We guarantee a surface-related presentation of the target epitope within the viral backbone.
This flexibility provides the advantage of inducing a highly potent and antigen specific immune response to the native target.
Human antibodies are essential drugs for manifold diseases and well accepted therapeutic formats. With our in-house developed in vitro immunization process we are able to activate human naïve B lymphocytes antigen-specifically within 12 days and fuse them afterwards to obtain immortal hybridoma cell pools. Target-specific screening of candidates is performed with selma.