Discover the Latest in Biomedical Research Innovation

Are you struggling to choose between the cost-effective MTT assay and the visually striking Live/Dead fluorescence staining? This guide breaks down the science, mechanisms, and pros and cons of the two most popular cell viability methods. Whether you are running high-throughput drug screenings or analyzing complex 3D spheroids, understanding the difference between metabolic activity and membrane integrity is key. Dive in to discover which assay reigns supreme for your specifi

CLYTE has officially joined the Google for Startups Cloud Program, a major milestone that validates its proprietary Sophie AI technology. This partnership grants CLYTE access to Google’s advanced computational resources, accelerating the release of Sophie 3.0 in January 2026. With enhanced reliability and deep-context analysis, CLYTE is redefining lab automation. The move sets the stage for a Q1 2026 Seed Round, signaling to investors that CLYTE’s tech stack is scalable and s

Discover how CLYTE is transforming biomedical research by aligning with the UN Sustainable Development Goals. From replacing disposable pipette tips with the reusable CytCut device (SDG 12) to democratizing access to the Soφ AI assistant (SDG 4), CLYTE is building a smarter, more sustainable future for science. Read how their specific innovations are solving the reproducibility crisis and driving global health progress.

Stop wasting time and money on endless minipreps! Colony PCR is the ultimate lab hack for molecular cloning, allowing you to rapidly screen bacterial or yeast colonies for your desired DNA insert in just a few hours. This definitive guide cuts through the noise and provides a detailed, step-by-step protocol for success. We dive deep into the one step most scientists get wrong—cell lysis and reveal primer design strategies!

This frustrating (and common) problem can ruin days of work, but the fix is often simple. Our comprehensive troubleshooting guide diagnoses the real reason for your patchy bands. We cover everything from the #1 culprit—air bubbles in your transfer sandwich—to aggregated antibodies, uneven gel polymerization, and improper sample prep. Stop guessing and start fixing. This article provides clear, actionable solutions to rescue your blot and get the clean, sharp bands you need.

Is your Western Blot showing a band at the wrong molecular weight? This is one of the most common frustrations in the lab, but it's not a dead end. An unexpected band size is often a critical clue, not a failed experiment. The theoretical calculated weight from amino acid sequence rarely matches the observed weight on a gel. This discrepancy can be caused by a host of biological reasons from post-translational modifications like glycosylation to protein cleavage, splice varia

Unlock the power of your clinical data with the Box and Whisker Plot! Learn the definitive step-by-step method for calculating the five-number summary—Min, Q1, Median, Q3, Max—and visualizing data distribution. From identifying critical outliers using the 1.5 x IQR rule to comparing drug efficacy in biomedical research, this guide is your key to superior data visualization that ranks and informs. Stop relying on means alone. Start seeing your data's true spread!

When your antibody fails to detect a signal, the problem can be complex. Is it the antibody itself? The sample? Or the protocol? This guide provides a complete troubleshooting protocol for "no signal" Westerns. We dive into the most common reason for failure and then provide a systematic checklist. Learn how to diagnose issues with your transfer using Ponceau S, why your blocking buffer might be the culprit, and how one common preservative could be killing your signal.