Webinar Banner: Top 6 Blind Spots Of Antibody Discovery and Development

In this webinar, you will learn:

  • Six frequently missed observations with critical impacts on antibody validation, hit selection and candidate characterization efforts.
  • Antibody biochemistry tips for design of SPR, and mass spectrometry-based epitope mapping workflows.

Characterizing Antibody Epitopes: What the Experts Say You’re Missing

In this webinar, we review 6 frequently missed observations in early pre-clinical antibody development that translate to failed antibody candidates in later stages. Our insights here are derived from hundreds of antibody interaction studies, across dozens of antibody formats and therapeutic modalities. They are applicable to most antibody discovery and development campaigns.

Recent improvements in antibody discovery and development technologies have allowed an increase in scale – producing more diversity and promising intelligent selection of the best hits. But to achieve scale and efficiency, the assays intended to validate binding, kinetics, epitope and other basic specifications are often run with a generalized set of parameters. As a result, many complex antibody interactions are interpreted through simple binding models, often missing valuable mechanistic insights.

Here, we will break down some of the most overlooked complex binding modalities – how to detect and validate them as well as what impact they might have on your antibody development. We hope that you can learn from these unexpected results, which significantly influence antibody characterization. Please join us to learn from real HDX-MS and SPR case studies and improve the quality and confidence of your antibody characterization data.

Speaker Bios

Live Webinar

Top 6 Blind Spots of Antibody Discovery and Development
Crucial experimental design and optimization techniques for antibody kinetics, binding, epitope mapping and biophysical characterization.

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