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How to use Soφ for Scratch Assay Analysis: The Best Tool for Cell Migration Measurement
Discover the future of cell biology through a researcher's eyes. This guide follows the journey from manual ImageJ struggles to AI-driven mastery. Learn how Soφ AI 3.0’s Scratch Analyzer processes 20 images in under a minute, determines statistical significance, and even drafts your conference poster results. Perfect for scientists looking to eliminate bias and reclaim their time.
6 days ago3 min read


Alternative to ImageJ for Easy Cell Migration Analysis
Stop wasting hours on manual ImageJ thresholding. Sophie AI 3.0 introduces a "Zero-Click" Scratch Assay Analyzer that quantifies cell migration in seconds. With batch processing, AI-driven edge detection, and instant statistical reporting, it's the modern replacement for Fiji. Learn how to automate your wound healing assays and eliminate user bias today.
7 days ago4 min read


AI Tool For Wound Healing (Scratch) Assay Cell Migration Analysis
The wait is over: Sophie AI 3.0 has arrived. Featuring the revolutionary Scratch Analyzer, this update is set to replace manual ImageJ workflows with high-speed, AI-driven automation. Whether you're troubleshooting a failed Western blot or quantifying complex cell migration, Sophie 3.0 acts as your digital "sue chef," ensuring every experiment is reproducible. Stop wasting hours on manual thresholding and start accelerating your research with CLYTE’s latest innovation.
Jan 273 min read


Step by Step Calculating and Interpreting IC50 & EC50 Values in Cell Viability Assays
Struggling with IC50 calculations? Accuracy starts before the assay. This guide covers everything from standardizing cell growth with CLYTE's Doubling Time Calculator to generating precise IC50 values. Stop guessing and start validating your research with the ultimate protocol for dose-response analysis.
Jan 264 min read


Hemocytometer Cell Counting & Seeding Calculation Made Easy
Stop doing math in the lab! Our Ultimate Guide to Hemocytometer Cell Counting breaks down the gold-standard protocol for accuracy and integrates CLYTE’s Free Biomedical Calculators to automate your seeding recipes. Whether you're tracking Doubling Time or seeding 96-well plates, this guide ensures your data is reproducible and error-free. Master the "Newton's Rings" technique and ditch the scratch-pad calculations today.
Jan 214 min read


The Ultimate Guide to Cell Doubling Time: Formula & Calculator
Stop guessing your cell seeding densities! Consistent experiments start with accurate cell growth kinetics. This guide breaks down the "Cell Doubling Time" formula, explains why it matters for reproducibility, and provides a step-by-step protocol for measuring it. We also introduce the CLYTE Cell Doubling Calculator—a free tool that automates the math so you can hit perfect confluency every time. Master your culture conditions and eliminate experimental drift today.
Jan 124 min read


Biomedical Calculations Made Easy: Guide to Cell Seeding, Doubling, Concentration, & IC/EC50 with CLYTE Calculators
Stop wasting hours on manual lab math! Discover the ultimate guide to CLYTE’s free Biomedical Research Calculators. From automating cell seeding recipes and calculating IC50/EC50 values to generating linear regression standard curves, this suite streamlines your workflow. Learn how to eliminate calculation errors and boost experimental reproducibility today.
Jan 74 min read


Guide to Mycoplasma-Free Cultures: Mycoplasma Testing Protocol
Mycoplasma contamination is the silent killer of research. This invisible threat doesn't make your media cloudy, but it systematically destroys the validity of your experiments by altering cell metabolism and gene expression. How do you fight an enemy you can't see? This article provides a complete, SEO-optimized protocol for Mycoplasma testing in cell culture. We dive into the "why" and "how" of detection, comparing the gold standard culture method with rapid PCR and visual
Nov 14, 20258 min read


10 Reasons Your Cells Won't Attach to the Flask : Low Adhesion and How to Fix It!
Are your cells refusing to stick to the flask? You're not alone. This frustrating problem can derail your experiments and leave you scratching your head. But fear not! Our in-depth guide explores the top 10 reasons for poor cell attachment, from problems with your culture vessel to issues with cell health, media, and more. We'll help you troubleshoot the adhesion problem and get your cells back to doing what they do best: growing and dividing.
Oct 15, 20257 min read


Break the Ice: How to Thaw Frozen Cells for Optimal Viability
Unlock the full potential of your cryopreserved cells with our definitive guide to thawing. From the crucial first moments in the water bath to the final plating, we'll walk you through the essential steps and best practices to ensure maximum cell viability and a successful start to your experiments. Learn the secrets to reviving your frozen cells and set your research up for success.
Oct 3, 20254 min read


CLYTE: The AI-Powered Biotech Startup Revolutionizing Biomedical Research
CLYTE, a trailblazing AI-biotech startup, is revolutionizing biomedical research. With groundbreaking innovations like the AI lab assistant Soφ, the precision tool CellCut, and the upcoming cell culture monitor Cadmus, CLYTE is tackling inefficiencies and enhancing research standardization. Their unique "First-Client Initiative" offers researchers free access to beta products, fostering a collaborative approach to scientific discovery and accelerating the pace of healthcare i
Sep 26, 20253 min read


Is Overconfluency Ruining Your Wound Healing (Scratch) Assay? How to Fix Peeling Monolayers
Frustrated by peeling monolayers and mysterious gaps ruining your scratch assay? Don't discard that plate just yet! A single variable in your setup is the likely culprit, sabotaging your results before you even make the scratch.
Uncover the simple cause behind monolayer detachment and learn the essential techniques to guarantee flawless, reproducible data in every single well. The definitive fix is inside.
Jul 18, 20254 min read
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