Electrophoresis is one of the widely used techniques in molecular biochemistry, microbiology and also for disease diagnosis.
Electrophoresis is similar to other separation techniques like chromatography but it differs in-terms of the types of samples analysed, the method used for separation, principle used etc.
Electrophoresis is a method of separation of charged molecules in an electric field so as to make them migrate towards opposite charged electrodes. The migration is due to charge on the molecules and potential applied across the electrodes. These molecules migrate at different speed and to different lengths based on their charge, mass and shape.
Types of electrophoresis & their techniques.
Electrophoresis can be broadly divided into 3 types
- Zone electrophoresis
Zone electrophoresis: Here the charged particles are separated into different zones or bands. This is of two types as
- Paper electrophoresis.
- Gel electrophoresis.
Paper electrophoresis is a techniques which employs a Whattman filter paper No.1 which is moistened by a buffer and then connected at two ends to two opposite charged electrodes. Then sample is applied on to one end and let for separation of components under electric field. After separation, the paper is dried and stained to get colored bands. These colored bands are recognized for the nature of sample by comparing with the standard. For a sample of serum, 5 bands of proteins can be separated by paper electrophoresis.
Gel electrophoresis is a similar techniques wherein instead of paper, a gel made of agarose or SDS (sodium dodecyl sulphate). The separation is more efficient than paper type as the rate of movement is slow and area of separation is larger by thickness. The sample is applied and subjected to electric field which can lead to separation of molecules. These molecules form bands and can be recognized by staining and comparing with standard sample bands. The method is more effective than paper and for instance from serum sample, 15 proteins bands can be isolated.
Isoelectro-focusing: Here the isoelctric pH is set at different foci and hence the molecules are immobilized to their isolecltric point. They don’t move towards electrodes but stay at a specific isoelectric pH. This is even more efficient to separate proteins and from serum, 40 bands of protein can be formed.
Immuno electrophoresis: This is the method with combination of principles of both electrophoresis with immune reactions. First the proteins are separated on to the electrophoresis paper. Then the antibodies are allowed to diffuse through the paper and react with separated protein molecules in bands.