Hot, Frozen, Sublimed and Blown: Biological Sample Storage Methods Summarized – Part One

Hot, Frozen, Sublimed and Blown: Biological Sample Storage Methods Summarized – Part One

I’ve recently been doing some lyophilization of biological extracts. While I was preparing for the experiment, I became interested in the number of different methods there are for drying, concentrating and storing samples: freezing, freeze-drying, rotary evaporation, centrifugal evaporation and blow down drying. Here is a brief description of each technique for biological sample storage…

Hot, Frozen, Sublimed And Blown: Sample Storage Methods Summarized – Part Two

Hot, Frozen, Sublimed And Blown: Sample Storage Methods Summarized – Part Two

In part one, I discussed the ‘how to’ of simply freezing samples and the basics of vacuum evaporation, often referred to as speed vacing. Now, we’ll have a look at two more complex sample storage techniques (at least in terms of equipment) for drying samples (lyophilizaton and rotary evaporation) and the simpler method of blow…

The Multi-skilled Scientist: Key Skills for All Scientists to Master

The Multi-skilled Scientist: Key Skills for All Scientists to Master

Although bench work is an integral part of becoming a successful scientist, it is by no means the only part of it. It is often the uncredited skill set possessed by many seasoned scientists that make them so valuable to employers and to further research. In this article I will highlight the less obvious skills…

The Five Essentials of Organizing Laboratory Samples

The Five Essentials of Organizing Laboratory Samples

If you look closely, there’s a scenario that plays out frequently in labs across the world: A scientist sits hunched over dry ice searching exhaustedly through frozen boxes for one sample that has disappeared into the abyss. The tube or specimen in question was likely catalogued at some point in time. But, between then and…

The Art of Approval: Getting a New Protocol Approved by Your Institution

The Art of Approval: Getting a New Protocol Approved by Your Institution

All of your planning has paid off. You just got the green light from your PI to start work on a new experiment that you have been plotting for weeks, but it involves some new techniques that you’ll need to run past your institution’s scientific approval committee first. No problem, right? Not necessarily. While many…

How to Minimize Variation and Achieve Reproducibility

How to Minimize Variation and Achieve Reproducibility

Ever wonder why your data isn’t the same after repeating an experiment? Well part of science’s beauty lies in the difficulty of achieving reproducibility. Heraclitus first said that no mans steps in the same river twice and the same can be applied to experiments. It is literally impossible to control for everything because the second…

The Dos and Don’ts of Weighing Dangerous Chemicals

The Dos and Don’ts of Weighing Dangerous Chemicals

A lot of chemical reagents are relatively non-hazardous.But there are just as many that are extremely hazardous, which means you’ll want to take precautions to reduce any risk of exposure, repeated exposure, and of course, accidental contamination of anything – or anyone – that walks out of the lab at the end of the day….

Let’s Dish About Soaps: A General Overview of Detergents

Let’s Dish About Soaps: A General Overview of Detergents

What do cell lysis, clean dishes, and gallbladders all have in common? Answer: detergents! These useful chemicals can solubilize fats and other proteins in water. They are the key to applications as varied as lysing cell membranes, extracting DNA, and solubilizing proteins for gel electrophoresis. To help you understand these important chemicals, we provide a…

Heating up agar? Just add a cup of water and avoid the glitter and crumbs

Heating up agar? Just add a cup of water and avoid the glitter and crumbs

It’s ironic how much folklore and superstition comes with being in science. “That’s a lucky pipette”, “playing Bach for your cells will help them grow”, “always make your own solutions”; we all have our own tips. Some of them might be well-founded others not so much… Tips from trusted colleagues can be very helpful though….

Facing Your Laboratory Freezer: Dos and Don’ts For Defrosting Day

Facing Your Laboratory Freezer: Dos and Don’ts For Defrosting Day

Your stomach clenches. Sweat snakes down your torso. The world seems to slow down. You begin the long, terrifying walk down the corridor. Your mind calls out to you to, “Run! Run now!” but you soldier on until you reach the door and knock. There is no escaping the wrath you will evoke when you…

Red light/Green Light In Aseptic Technique: When Is The Flame OK?

Red light/Green Light In Aseptic Technique: When Is The Flame OK?

My mom is a microbiologist and so I was a lot more informed about bugs than most kids. In fact, I probably gave more than one classmate nightmares with my talk of there being 10 times more bacteria that make up the human body than human cells. I remember my mom working by a Bunsen,…

Agarose versus Polyacrylamide: Not All Gels Are Created Equal

Agarose versus Polyacrylamide: Not All Gels Are Created Equal

Like athletes running on turf versus sand, the gel you run your DNA through can highly affect your results. The two main types of gels that people use for DNA electrophoresis are agarose and polyacrylamide (PA) gels, but figuring out the differences can be confusing. Basically, you choose a gel based on two main factors:…

Gel Electro-For-Whatsit?  Breaking Down How Gel Electrophoresis Works

Gel Electro-For-Whatsit? Breaking Down How Gel Electrophoresis Works

Run to red!  It’s a mantra I learned when first using gel electrophoresis to separate DNA molecules.  This can save you a lot of frustration and humiliation in the lab (stage right: a complaining scientist who swears the equipment is broken as a supervisor facepalms in embarrassment). But what about how does this jell-o like…

freeze thaw dog, plasmon resonance implications

Freeze-Thaw Cycles and Why We Shouldn’t Do It

Freeze-thaw—you know it’s bad for your samples, don’t you? While working in the lab, you have most likely heard someone say ‘aliquot your protein/cells/DNA/RNA to avoid too many freeze-thaw cycles.’ But do you actually understand why? You probably thought that avoiding freeze-thaw cycles had something to do with damaging cell structure as well as proteins…

Buying a Secondary Antibody:  Why all the Choices?

Buying a Secondary Antibody: Why all the Choices?

So you grab a quick 5 minutes in between lectures to sit down and tackle an item on your to-do list: order a secondary antibody for an upcoming experiment.  But when you start to search your favorite secondary antibody provider’s website, you realize it is not going to be a 5 minute job.  Conjugated, F(ab’)2…

Tips for Heating up Agar in the Microwave

Tips for Heating up Agar in the Microwave

One of our readers posted the following question to us and we decided to pass it along to everybody’s favorite microbiology expert, Aunt Yersinia: For one year I am working in different research laboratories, after I got from school. I keep wondering why EVERYBODY is using pre-made Agar solutions for pouring plates, and EVERYBODY is…

What Makes a “Good” Laboratory Buffer?

Just about any molecular biology experiment will involve the action of enzymes or other active proteins. And when enzymes are involved, the pH of your experimental environment is going to change. This is because most enzymatic reactions involve the loss or gain of hydrogen ions (protons), which modifies the pH of the environment. Biological systems…

A Quick Primer on Enzyme Kinetics

A Quick Primer on Enzyme Kinetics

As biological catalysts, enzymes transform target substrates into products. Enzyme kinetics is the rate of that transformation. By understanding how an enzyme’s behavior is affected, you can figure out how it functions in physiology or fails to function in disease. Now it gets complicated… What Affects an Enzyme’s Kinetics? In the first place, most enzymes…