Learn about CIS Display™, a powerful antibody selection tool
CIS Display™ is a cell-free alternative to traditional phage display methods. Uncover the power of an antibody selection tool optimized for our ultra high-diversity libraries and advanced small format scaffolds like Centyrins and VHHs


What is CIS Display™?
Unlike phage, yeast, or mammalian display, CIS Display™ does not involve a biological system. This means that library sizes are less restricted and that larger libraries can be mined effectively.
Originally developed by a team at Isogenica including our current Non-Executive Director Dr. Bill Eldridge, CIS Display™ was first designed to interrogate high-diversity peptide libraries. Over time, this was extended very successfully to increasingly complex small format scaffolds such as Centyrins and VHHs.
Why do we use CIS Display™?
- Display Capacity: Because CIS Display™ is completely cell-free, our synthetic library sizes aren’t limited by a transformation step. This means we can not only create huge libraries, but we can mine them effectively too.
- Scalability: Driven by PCR reactions, we can enrich many different panning arms simultaneously, via our HTP automation. This allows us to experiment with a wider set of conditions such as antigen concentrations, epitope masking, or specific elution to give us the best chance of finding the right conditions to drive towards a TPP.
- Big Data: By seamlessly integrating next-generation sequencing (NGS) analysis, we benefit further from the additional diversity of our libraries, allowing enrichment analysis and identification of rare binders – particularly important with more challenging targets such as membrane proteins.
To learn more, get in touch today.
Publications
CIS display, a DNA-based in vitro selection technology for therapeutic peptides
CIS display is a DNA-based in vitro display technology that enables the display and selection of peptides and proteins from extremely large libraries…
CIS display: In vitro selection of peptides from libraries of protein–DNA complexes
PNAS published February 23, 2004. 101 (9) 2806-2810