Abstract
Erythropoietin (EPO) quantification during cell line selection and bioreactor cultivation has traditionally been performed with ELISA or HPLC. As these techniques suffer from several drawbacks, we developed a novel EPO quantification assay. A camelid single-domain antibody fragment directed against human EPO was evaluated as a capturing antibody in a label-free biolayer interferometry-based quantification assay. Human recombinant EPO can be specifically detected in Chinese hamster ovary cell supernatants in a sensitive and pH-dependent manner. This method enables rapid and robust quantification of EPO in a high-throughput setting.
| Original language | English |
|---|---|
| Journal | Molecular Biotechnology |
| Volume | 57 |
| Issue number | 8 |
| Pages (from-to) | 692-700 |
| Number of pages | 9 |
| ISSN | 1073-6085 |
| DOIs | |
| Publication status | Published - 2015 |
Keywords
- Biolayer interferometry
- Chinese hamster ovary (CHO) cells
- EPO
- Erythropoietin
- Quantification assay
- VHH