Following electrophoresis, protein band patterns can be visualized and subjected to qualitative and quantitative analysis. Protein visualization is usually achieved through use of protein stains. Once the gel is stained, it can be photographed and analyzed using imaging instruments and accompanying software.
Related Topics: Protein Electrophoresis.
Gels are run for either analytical or preparative purposes. The intended use of the gel determines the amount of protein to load and the means of detection. It is most common to make proteins in gels visible by staining them with dyes or metals. Each type of protein stain has unique characteristics and limitations with regard to the sensitivity of detection and the types of proteins that stain best. Select protein stains based on their properties and your intended applications.
Often proteins are transferred to membranes for western blotting or other applications. Protein blots can also be visualized using stains. Find more information on blot detection and imaging in the western blotting section.
Before gels can be analyzed with an image evaluation system, they must be digitized. Digitization of gels stained with colorimetric, fluorescent dyes or radioactive compounds requires specific imaging systems (Patton 2000). The most commonly used devices are camera systems, densitometers, phosphor imagers, and fluorescence scanners. All of Bio-Rad's imaging systems are seamlessly integrated with analyis software (Image Lab™ and PDQuest™ software), and they can export and import images to and from other software via TIFF files.
You can visualize proteins on a gel in 5 mins without staining using Bio-Rad’s unique stain-free gel chemistry.
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