Beyond the Blot: Achieving Reproducible, Publication-Ready Protein Expression Data

Image manipulation scandals and tightening journal guidelines have put traditional Western blots under a spotlight: every manual step—from gel casting to image export—adds variability and opens the door to error. Simple Western™ Technology replaces the legacy membrane workflow with fully automated, capillary-based immunoassays that separate, detect, and quantify proteins in a sealed system, producing tamper-evident data in as little as three hours.

Join us to learn how laboratories worldwide are using Simple Western to address the life sciences reproducibility crisis. We’ll explore:

• Automation for consistency: how closed-capillary processing eliminates analyst-to-analyst variation and extends quantification across four orders of magnitude.

• Real-world example of Simple Western’s advantages over traditional methods in terms of sensitivity, reproducibility, productivity and sample volume requirement.

• Compass for Simple Western™ software: immutable run files that bundle electropherograms, lane views, and metadata for effortless peer review and data sharing.

• Built in Total Protein Normalization: Flexible total protein normalization strategies that enable consistent and accurate results and remove uncertainty around housekeeping controls.

Whether your goal is to strengthen grant applications, streamline journal submissions, or simply trust your blots again, this session will show how Simple Western delivers quantitative, reproducible protein data—without the blotting.