Zero Tolerance: A Perfectionist’s Guide to Aseptic Technique

Zero Tolerance: A Perfectionist’s Guide to Aseptic Technique

Arguably, molecular biology is impossible without microbiology—even if you work exclusively with transgenic mice, you may one day need to amplify a vector in E. coli. And microbiology is definitely impossible without good aseptic technique. The main principle of good microbiological practice is a zero tolerance approach: it’s good to be a little paranoid about…

Which Light Microscope Will I Choose? Part 1 – Basic Light and Fluorescence Systems

Think before you start! Before you even start preparing your samples, you should think about the choice of microscope for image acquisition. Manufacturers offer an ever increasing range of light microscopes- some of which may already be available in your research institutes. To help you get the best out of your imaging experiment by making the…

The Cell: An Image Library – An Overview of an Award-winning Multimedia Site

Much more than just an archive, The Cell: An Image Library-CCDB (Cell Centered Database; ‘The Cell’) serves many additional purposes. Whilst many researchers use The Cell to organize their own images for research and archival purposes- the real value of The Cell is the ability to share those images with other researchers. In many scientific…

Next Generation Sequencing Channel, A Revolution in Technology

Next Generation DNA Sequencing (NGS) is a revolutionary new technology that provides biologists and medical scientists with the ability to collect massive amounts of DNA sequence data both rapidly and cheaply. This technology is having a huge impact on many aspects of biology and medicine because it can be applied in so many different ways….

How Pure is Your Cell Culture Broth? Comparing Mycoplasma Detection Kits

How Pure is Your Cell Culture Broth? Comparing Mycoplasma Detection Kits

Mycoplasmas are the most difficult-to-detect organisms in your eukaryotic cell culture. And they can be the most dangerous; they can disrupt cell growth and differentiation and even apoptotic patterns without you even knowing what’s going on until it’s too late. Traditional cell culture methods can take up to a month to yield results, which means…

A Beginner’s Guide to Storing Biological Materials

A Beginner’s Guide to Storing Biological Materials

In a typical biology lab, you may encounter many types of biological materials, including cells, bodily fluids, purified DNA and RNA, enzymes, bacterial cultures, body parts, and whole animals. In order to perform experiments that yield quality results, samples need to be stored properly in order to preserve their activity or integrity. Beginning students and…

How to Transform Your Images from Mediocre to Publication Quality with Köhler Illumination

How to Transform Your Images from Mediocre to Publication Quality with Köhler Illumination

You’ve spent days, perhaps weeks or months squirrelling away tubes of preserved tissue in the dark drawers under your laboratory bench like the trophies of a demented serial-killer. Hours have been spent in histology in the processing, embedding and sectioning onto slides. Finally, like a warrior victorious in battle, you hold aloft your thin glass…

Got Phage? Here’s how to get rid of it.

Got Phage? Here’s how to get rid of it.

Summertime… The birds are singing, the trees are growing. Your tissue culture has sprouted yeast contamination, your yeast culture is happily growing bacteria. Your bacterial culture was growing calmly and predictably, dividing every twenty minutes, but suddenly its optical density has dropped, and it’s full of some sort of filaments and clumps. Or you did…

Quick Protocol: How to Work Safely and Effectively with a Biological Safety Cabinet / Culture Hood

Before using any Biological Safety Cabinet (BSC) for the first time, have a person with working knowledge of the machine give you an overview of how to use the cabinet. Different labs have different protocols in regards to running the cabinet, disinfecting the cabinet, determining which pathogens that may be used in the cabinet and…

3 Ways to Abuse Biological Safety Cabinets

3 Ways to Abuse Biological Safety Cabinets

As we learned in my previous article, cell culture hoods have many names. As if that wasn’t enough, they are all-too-often misunderstood and mistreated, which can lead to dangerous situations harmful for both the worker and the general lab environment. Here are three common ways that workers abuse biological safety cabinets; make sure you don’t…

Biological Safety Cabinets and Culture Hoods: Know The Difference

Biological Safety Cabinets and Culture Hoods: Know The Difference

Biological safety cabinets, laminar flow hoods, clean hoods and culture hoods are all common names for those essential pieces of equipment that you use in cell culturing. The terms are used inter-changeably, but in fact there are lots of different types of culture hoods, each of which does a different job. Knowing which is which…

5 Ways to Delay The Publication of Your Manuscript

Most scientists I know approach the publication process with fear and trembling: the endless discussions about what journal to submit to, the agonized consideration of impact factors, comparing the all-important “time to first decision”, etc. Now that I’ve been working for a scientific publisher for a few months, I’m surprised at how many manuscripts still…

4 Tips for Better Scientific Image Processing in Photoshop

For scientists, Photoshop is a double-edged sword with a dagger nailed to the hilt. Its power in image processing is unrivalled; its ability to gut you with ethics violations is unmatched. An earlier article outlined how to keep your conscience clean when Photoshopping, here we offer four tips that will help walk with the Photoshop balancing…

The Easiest Yeast Transformation Protocol on Earth

The Easiest Yeast Transformation Protocol on Earth

There are several yeast transformation protocols around, and most of them require a lot of steps: overnight starter culture, dilution and growth to logarithmic phase, several washes, and so on… These protocols work very well since they have been optimised for maximum transformation efficiency, which is needed for applications like library construction. But they are…

How Proteases and Protease Inhibitors Work

How Proteases and Protease Inhibitors Work

Proteases: wild, mysterious, destructive.  What are these untamed elements ravaging your precious lysate? How can a drop of EDTA or a smidge of “cocktail” protect that sample, which is gently cradling your hopes, your dreams, and your desire to survive the next lab meeting? Brace yourself for a biochem flashback: in this article, we’ll explain…

How to Present Successfully at Conferences

The very idea of standing up and giving an oral presentation at a conference gives even the most confident of us butterflies. Additionally, I don’t know many scientists who find the thought of spending hours working on a powerpoint presentation exactly thrilling. However, there are many benefits to presenting your work at a conference. First…

A Crash Course in Epigenetics Part 4: Disease mechanisms and therapeutic targets

A Crash Course in Epigenetics Part 4: Disease mechanisms and therapeutic targets

After having discussed what epigenetic mechanisms are and how we’ve learnt about what they do, it is now time to look into how epigenetics affect our lives if things do not go the way they are supposed to go. I hope I have convinced you that epigenetic processes are vital for an organism, in development…

A Crash Course in Epigenetics Part 3: Regulated regulation

A Crash Course in Epigenetics Part 3: Regulated regulation

Epigenetics is the most rapidly expanding field in biology. In the second article in this series, I discussed which experimental techniques have been crucial in gaining insight into epigenetic processes. I will now shed light on what those and other methods have taught us. As described in the first article, it has been long understood…

A Crash Course in Epigenetics Part 2: The toolbox of the epigeneticist

A Crash Course in Epigenetics Part 2: The toolbox of the epigeneticist

In the past decade, important advances have been made in the field of epigenetics. Obviously, unraveling epigenetic mechanisms has been greatly facilitated by technological developments. I’ll try to give you an impression of the types of experiments that have helped fuel those new and exciting insights. Yevgeniy Grigoryev has recently written an article on DNA…

A Crash Course in Epigenetics Part 1: An intro to epigenetics

A Crash Course in Epigenetics Part 1: An intro to epigenetics

These days, epigenetics is a fast moving field. I don’t remember having learnt about it during my biomedical studies, some 10 years ago. Nowadays, there seems to be no way around it when studying health and disease. Increasing interest combined with recent technological breakthroughs have led to quickly expanding knowledge of its abundant and important…

An image of colors to depict care for your pH meter.

“What You Should Know About Science” — A Book Review of ‘The Golem’

I first read “The Golem: What You Should Know about Science” as an undergraduate student for an introduction to the sociology of scientific knowledge. I feel it’s an important book for anyone who wants to understand how science works. Ten years later, I still find myself revisiting it. Read on to find out why… In…

The Invisible Horde: Attacking Mycoplasma Infections

Mycoplasma infections are very, very bad news; these special prokaryotes can rapidly spread through your cell culture and inhibit cell proliferation, induce apoptosis, cytokines and radicals, and otherwise transform your cells. Worst of all, since contamination is not easy to spot, you may not realize your culture is contaminated until it’s too late. The 100…

How to to Speed up Commercial Midi and Maxi Plasmid Preps

How to to Speed up Commercial Midi and Maxi Plasmid Preps

Commercial kits for isolation of large quantities of plasmid DNA generally rely on standard alkaline lysis followed by an affinity chromatography column-based method to purify DNA. Compared to traditional cesium chloride banding or PEG precipitation of plasmid DNA they are a breeze, and have the added benefit of avoiding use of toxic or hazardous chemicals…

Wasting Antibodies Doesn’t Float Your Boat? Try Floating Your Blot Instead!

Western blots may be great for visualizing protein expression, but they can be a perfect way to waste your precious antibody stocks if you follow the normal protocol. Thankfully, you don’t have to follow the normal protocol any more; here’s how to get great blots with a fraction of the antibody usage. I have tried…

Is Your Science Making an Impact?

It’s pretty likely you’ll have heard of impact factors, either through colleagues talking about them in the lab, or from a journal homepage advertising its latest score. Whilst impact factor is a relatively artificial value, it is something that journal editors, scientists and some funding agencies take seriously. It’s therefore important to understand what it…

Film vs. Digital: A Real Western (Blotting) Showdown

Film vs. Digital: A Real Western (Blotting) Showdown

You’ve masterfully run and transferred your gel, and now it’s time to probe and quantify your protein(s). You’ve got your antibodies and ECL ready to go. Substrate – check. Film cartridge – check. Darkroom – ah yes, that magical place where night vision goggles are required to navigate a veritable minefield of potential chaos. It…