How To Passage Cells in Culture
Learn the basics of how to passage cells in culture with this easy-to-follow guide. While the specifics change per cell line, the basics remain.
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Learn the basics of how to passage cells in culture with this easy-to-follow guide. While the specifics change per cell line, the basics remain.
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We often use size-exclusion chromatography to purify samples. Read this article to learn how to use it to measure sample molecular weight as well!
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Want to use a cell line but not sure where to start? Or perhaps you’re just curious about the most commonly used cell lines. Our top 5 most commonly used cell lines will help you get a feel for the cells that many researchers turn to.
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While using serum in cell culture can keep your cells healthy and happy, there are some notable downsides. We discuss the pros and cons of using serum in cell culture media and how to remove it if you want to eliminate it from your workflow.
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We show you how to read a scientific paper efficiently to make the most of your reading time.
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Buffers provide a stable chemical environment for all our experiments. But how do buffers work? And how do you pick one? Read on to find out.
Getting involved in the post-publication review of scientific papers can seriously improve your critical analysis skills. Here’s how.
Working with chemicals is dangerous and can lead to injury, or worse. Follow these ten broadly applicable golden rules to help keep you and your colleagues working safely in the lab.
Here’s an easy guide on how to maintain your lab balance. Following these tips will ensure your balance remains clean and perhaps most importantly, accurate.
In biosciences, we purify our target molecules using chromatography. So, we need a thorough understanding of how chromatography works!
You may be familiar with standard single fragment ligations, but did you know you can ligate multiple fragments into your vector all at the same time! Discover how to perform multiple fragment ligation, including the different methods and troubleshooting tips for when things go wrong.
Contamination in your pipette can mean contamination in your experiments, making cleaning pipettes regularly critical. Here’s an easy guide on how to do it.
Want to know the best way to perform relative quantification for your qPCR data? Read on.
Kits for DNA gel extraction are a great way to save time in the lab, but they are costly and produce much plastic waste. Discover three easy kit-free DNA gel extraction methods that can save you money and reduce waste in the lab.
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Let’s be honest—we scientists don’t always present our science in ways that are accessible to everyone. Nor is lab-based science always accessible. Explore what accessibility in science is and how we can all make science more accessible and inclusive.
Acids are common and essential chemicals in any research laboratory. In this article, you’ll get advice on how to handle strong acids safely to give you the confidence to routinely prepare, handle, and dispose of them in the lab.
I’d bet that your trusty pipette is probably one the the most often used tools in the lab. But do you have any idea how to check the accuracy of your pipette? We’ll take you though how to do this in just 7 easy steps.
Pouring and running an agarose gel should be a simple and routine procedure, but there are a surprising number of ways to destroy your agarose gel.
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