I imagine, you know, once you get past affinity and specificity, we're just trying to like systematically remove as many of the downstream like gotchas and surprises that keep drugs from ultimately making it to commercialization. And I would imagine over the years, people have always kind of had this like, maybe it's hubris, but maybe it's also just strategy or thinking about the problem. Is there a set of unknown unknowns with antibody development where no one is really paying attention? We don't have technology to scale up being able to screen for vis viscosity in a kind of a high throughput manner. That could potentially be an blind spot for us later on down the road

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