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

Build a CV You Can Be Proud Of – Part I: Communication Skills

They say scientists are highly skilled… and rightly so! While many people would think that we’re shy, retiring types who sit at our lab benches obsessing over teeny-weeny molecules, science (and particularly the process of obtaining a PhD) sets us up as highly skilled members of the workforce. I can hear you all groaning as…

An Introduction To ChIP-seq

An Introduction To ChIP-seq

ChIP-seq is a wonderful technique that allows us to interrogate the physical binding interactions between protein and DNA using next-generation sequencing. In this article, I’ll give a brief review of ChIP and introduce the chromatin immunoprecipitation sequencing technique (ChIP-seq), which combines ChIP with next-generation sequencing. What is chromatin immunoprecipitation? Chromatin immunoprecipitation (ChIP) allows us to…

How to transfer one SDS-PAGE gel onto two membranes

How to transfer one SDS-PAGE gel onto two membranes

Have you ever wished you could transfer the same SDS-PAGE gel twice? Sometimes, when you are blotting for many different proteins of similar size, stripping and reprobing multiple times can become impractical.  Here’s a simple diffusion transfer method that can be used to generate duplicate membranes from a single gel: Protein transfer by this diffusion…

Detecting Protein Phosphorylation Without Radiation Phospho Specific Antibodies Or Mass Spec

Detecting Protein Phosphorylation Without Radiation Phospho Specific Antibodies Or Mass Spec

Phosphorylation is one of the major post-translational modifications that regulate the activity of a protein. Around a third of human proteins are believed to be phosphorylated, and so the kinases and phosphatases that mediate protein phosphorylation are of major interest to biomedical researchers. However detecting protein phosphorylation can be difficult, particularly from cell extracts. Phospho-specific…

A Primer on Statistical Hypotheses

A Primer on Statistical Hypotheses

Hypothesis testing is the foundation around which we prove our science is worth funding, publishing and sitting through a conference presentation for. I can’t overstate the  importance of understanding hypothesis testing, such is the integral part it plays in biological analyses. The Null Hypothesis Fundamental to statistics is the concept of a null hypothesis, and…

Train Yourself to Measure OD600 by Eye: An Improved Approach

Train Yourself to Measure OD600 by Eye: An Improved Approach

Back in August I shared my training regimen for guesstimating the OD­600 readings of microbial cultures with superhuman accuracy. Although my method is effective, I will admit that it has two shortcomings: you need to make a separate standard curve for each container type, and guesstimation is not an officially sanctioned scientific method. But now,…

Six Fixes For Antibody Co-Elution In Immunoprecipitations

Six Fixes For Antibody Co-Elution In Immunoprecipitations

Do you want to immunoprecipitate (IP) a protein with a molecular weight that is anywhere near 55 kDa or 25 kDa? Then you have an irritating problem to deal with: antibody co-elution. But don’t panic, we have six strategies for dealing with your new problem. The Problem: Typically, the IP antibody is bound to Protein…

5 Sure-Fire Ways to Screw Up Your RNA extraction

5 Sure-Fire Ways to Screw Up Your RNA extraction

Working with RNA is definitely an acquired skill.  It’s a lot more finicky than working with DNA, and requires careful attention to detail in order to avoid disastrous through RNase contamination.  Here are a few common ways to lose your hard-earned RNA:  1. Don’t keep everything on ice Keeping the temperature of all of your reagents cool is…

10 Things You Need to Know About Restriction Enzymes

10 Things You Need to Know About Restriction Enzymes

Restriction enzymes are a basic tool in the molecular biologist’s arsenal.  They’re super easy to use, and virtually essential for cloning and other applications.  Restriction enzymes are also a great example of a perfect “tool” from nature that scientists have co-opted for their own use.  Here are a few fun facts about restriction enzymes that…

The Pros and Cons of a PhD or Post-doc in a Foreign Country

The Pros and Cons of a PhD or Post-doc in a Foreign Country

It’s time to start thinking about your next move. Maybe you’ve finished your undergrad/master’s degree and are considering doing a PhD. Or maybe you’re past all that and need to find a post-doc position. Amongst all of this, you might be considering the option of doing your PhD or post-doc in a foreign country. It’s…

Careers for Scientists – Research Technician

Careers for Scientists – Research Technician

One of Bitesize Bio’s regular readers asked me to interview people in jobs that don’t necessarily require a PhD.  So, today I’m talking to Angela Briski who’s a research technician and currently working in stem cell research.  Hope you enjoy the interview… You describe yourself as a Research Technician.  And what exactly is it that…

Three Approaches to Site-directed Mutagenesis

Three Approaches to Site-directed Mutagenesis

Site-directed mutagenesis studies can be extremely useful for elucidating the function of a gene or protein, or for creating variants of an enzyme with new and improved functions. There are now many approaches available for generating site-directed mutants, whatever your purpose. In this post I’ll summarize three techniques that will enable you to produce a…

Clean-up or Fraud? How to Avoid Photoshopping Your Way Into Disgrace

Thanks to the power of digital imaging software, faking data is a lot easier than doing real science. Clearly the honest majority of us would never deliberately distort the scientific record, but is it possible to stumble into trouble through sheer ignorance? Quite possibly. The line between innocent enhancement and deliberate fraud can be blurry…

Make Your Manuscripts More Readable in 5 minutes per Day

We scientists are all so focused on getting our work published that many of us seem to forget something very important; that publication is just the beginning. After publication is when our manuscripts really have to do their essential work of communicating our science to our peers. If no-one reads the manuscript, we might as…

Use Less Vector, Killer Cut for Success in Plasmid Cloning

Here’s an all-too-often repeated scene in the lab: First thing in the morning, you approach the 37°C incubator with trepidation, open it and through one half-open eye you take a look at the LB plate that you spread your ligation-reaction-transformed E.coli aliquot onto. Looks good – thousands of colonies. Emboldened, you take your “no ligation…

Should You Use Magnetic Beads for Immunoprecipitation?

Should You Use Magnetic Beads for Immunoprecipitation?

Sepharose beads are porous, which gives them a high surface area for interaction with proteins and allows them to hold a lot of liquid. This is perfect for the application that they were originally designed for: purifying milligrams of protein in columns. When immunoprecipitation (IP) – a small-scale technique for pulling specific proteins out of solution using…

Working with Enzymes:  Part I -The Simple Kinetic Spectrophotometric Assay

Working with Enzymes: Part I -The Simple Kinetic Spectrophotometric Assay

At the end of my last article, I provided some practical tips and tricks for working with enzymes at the bench. Now, we’ll cover one of the cornerstone techniques of enzymology work: the enzyme assay. Starting with the simple assays and eventually working our way to the more complex, this article introduces the principles of…