YUMAB® Antibody Libraries

Universal YUMAB® human antibody libraries comprise more than 100 billion (1011) unique antibodies. In combination with our advanced in vitro selection technologies, we provide highest success rates to obtain the desired antibody candidates to any kind of antigen target.

Universal YUMAB® libraries contain natural antibody sequences (no synthetic sequences), which are close to the human germline repertoire. These antibody sequences are pre-selected in the human body for low toxicity, immunogenicity and high productivity, which makes them perfect for the development of therapeutic drugs.

YUMAB® libraries have a long track record and have proven their value and excellent quality in pharmaceutical pipelines when compared head-to-head with other commercial libraries.

YUMAB® Antibody Library Features

  • Natural antibody repertoires (no synthetic sequences)
  • Universal and broad repertoire (all human frame works and CDR lengths)
  • Large epitope coverage and high hit rate
  • Flexible business conditions

References – YUMAB® libraries

Miethe, S., Mazuet, C., Liu, Y., Tierney, R., Rasetti-Escargueil, C., Avril, A., Frenzel, A., Thullier, P., Pelat, T., Urbain, R., Fontayne, A., Sesardic, D., Hust, M. and Popoff, M.-R. (2016). Development of Germline-Humanized Antibodies Neutralizing Botulinum Neurotoxin A and B. PLoS ONE 11: e0161446 (PubMed)

Schieferdecker, A., Oberle, A., Thiele, B., Hofmann, F., Göthel, M, Miethe, S., Hust, M., Braig, F., Voigt, M., Koch-Nolte, F., Haag, F., Alawi, M., Indenbirken, D., Grundhoff, A., Bokemeyer, C., Bacher, U., Kröger, N. and Binder, M. (2016). A transplant immunome deep sequencing and screening platform defines a unique targetable epitope fingerprint of multiple myeloma. Blood 127: 3202-3214 (PubMed)

Kügler, J., Wilke, S. Meier, D., Tomszak, F.,  Frenzel, A. , Schirrmann, T., Dübel, S.,  Garritsen, H.,  Hock, B., Toleikis, L., Schütte, M. & Hust, M. (2015). Generation and analysis of the improved human HAL9/10 antibody phage display libraries. BMC-Biotechnology 15: 10 (PubMed)

Frenzel, A., Kügler, J., Wilke, S., Schirrmann, T. & Hust, M. (2014). Construction of human antibody gene libraries and selection of antibodies by phage display. Methods Molecular Biology 1060: 215-243 (PubMed)

Miethe, S., Rasetti-Escargueil, C., Liu, Y., Chahboun, S., Pelat, T., Avril, A., Frenzel, A., Schirrmann, T., Thullier, P., Sesardic, D. & Hust, M. (2014). Development of neutralizing scFv-Fc against botulinum neurotoxin A light chain from a macaque immune library. mAbs 6: 446-459 (PubMed)

Hust, M., Meyer, T., Voedisch, B., Rülker, T., Thie, H., Schütte, M., Helmsing, S., Meier, D., Schirrmann, T. & Dübel, S. (2011). A human scFv antibody generation pipeline for proteome research, Journal of Biotechnology 152,159-170 (PubMed)

Thie, H., Toleikis, L., Li, J., von Wasielewski, R., Bastert, G., Schirrmann, T., Esteves, I. T., Behrens, C. K., Fournes, B., Fournier, N., de Romeuf, C., Hust, M. and Dübel, S. (2011). Rise and fall of an anti-MUC1 specific antibody. PLoS ONE 6: e15921 (PubMed)

Pelat, T., Hust, M., Laffly. E., Condemine, F., Bottex, C., Vidal, D., Lefranc, M.P., Dübel, S. & Thullier, P. (2007). A high affinity, human like antibody fragment (scFv) neutralising lethal factor (LF) of Bacillus anthracis by inhibiting the PA-LF complex formation. Antimicrobial agents and chemotherapy 51, 2758-2764 (PubMed)


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Email: info@yumab.com
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