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Developing in vitro assays as close as possible to human physiology with a quantitative read-out.

  • Using our own iPSCs, modify them genetically if required and differentiate them to the desired cell type.
  • Using primary cells, modify them genetically if required to build the desired in vitro model.
  • Developing reporter systems that are integrated into the genome, which provides a quantitative read-out.

Examples include:

  • 3D epidermis model using primary keratinocytes with a reporter system for oxidative stress
  • in vitro model of the blood brain barrier using brain microvascular endothelial cells derived from iPSCs.

 

Generating antibodies against complex membrane proteins such as GPCRs and ion channels.

  • Using our rabbit cell lines to express the human protein of interest and our immunization protocol of rabbits with these cells, generating a strong immune response against the human protein in its native conformation.

Examples include:

  • Antibodies against GPR137
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