There is a plethora of uses for detergents, both in the lab and in everyday life. The usefulness of these cleaning compounds comes from subtle differences in their chemical structure. Detergents are composed of amphipathic molecules, containing a polar hydrophilic head group attached to a long-chain hydrophobic carbon tail. The composition and charge of the molecules’ head and tail groups determines the mechanism by which these molecules will act as detergents. Because of this, different types of detergents are useful for a variety of purposes.
The Protein Man

Recent Posts
Detergents: Ionic, Non-Ionic, and Zwitterionic. What's the Difference?
Topics: Detergents
Plant vs Animal Cells: Break the Cell Wall with Lytic Enzymes
Extracting proteins from plants is not the same as extracting proteins from animal sources. There is a very different set of factors that you will need to consider in order to properly process plant proteins. This post explores some of the key ways in which plant-based protein extraction differs from animal-based protein extraction, and details some of the ways you can overcome these differences.
Topics: Protein Extraction
Western blot: Constant current or constant voltage; which is best?
The choice of constant current or constant voltage will depend on several different factors that must be taken into consideration for each Western transfer test. The level of heat, duration of the test, type of proteins, the size of the transfer, and the rate of transfer will all be affected by power, voltage, and current being used to drive the test. Each factor will play a role in how well the proteins transfer and the ultimate accuracy of the test.
Topics: Western Blotting
Best Blocking Buffer Selection for ELISA & Western Blot
Antibodies are used to detect specific proteins during research. There are a variety of tests including the Western blot, that produce a surface area that can contain other proteins and components that need to be blocked. Blocking buffers are used to bind the surface areas that may attach to reagents during the testing process, preventing the non-specific antibodies from interacting with the reagents and causing a poor reading or inaccurate results. Knowing which buffers to use, however, is critical for ensuring the accuracy of a test, as each option has its own advantages and disadvantages.
Topics: Western Blotting, Assay Development (ELISA), Protein Detection