REVIEW ON ELECTROPHORESIS TECHNIQUES
4. Dielectrophoresis (DEP):
It is a phenomenon in which a force is exerted on a dielectric particle when it is subjected to non-uniform electric field. This force doesn’t require the particle to be charged. All particles exhibit dielectrophoretic activity in the presence of electric fields. However the strength of field depends on the medium and particles and on the particle’s shape, size as well as frequency of the electric field.
5. DNA Electrophoresis:
It is an analytical technique used to separate DNA fragments by size. DNA molecules which are to be analysed are set upon a viscous medium, the gel, where electric field induses the DNA to migrate towards the anode, due to the net negative charge of the sugar-phosphate back-bone of the DNA chain. The separation of these fragments is accomplished by exploiting the mobilities with which different sized molecules are able to pass through the gel.
6. Gel Electrophoresis:
It refers to using a gel as an anticonvective medium and/or sieving medium during electrophoresis. Gel electrophoresis is most commonly used for separation of biological macromolecules such as DNA, RNA or proteins. It refers to the movement of charged particles in an electric field. Gel suppress the thermal convection caused by application of the electric field, and can act as a sieving medium, retarding the passage of molecules, gel also can simply to serve to maintain the finished separation, so that a post electrophoresis stain can be applied.
7. Electro blotting:
It is a method in molecular biology/biochemistry/immunogenetics to transfer proteins or nucleic acids on to a membrane by using PVDF o\r nitrocellulose, after gel electrophorsis. The protein or nucleic acid can then be further analysed using probes such as specific antibiotics, ligands like lectins or stain. This method can be used with all polyacrylamide and agarose gels. An alternative technique for transferring proteins from a gel is capillary blotting.
8. Electro focussing:
Isoelectro focussing (IEF), also known as electro focussing, is a technique for separating different molecules by their electric charge differences. It is a type of zone electrophoresis, uaually performed on proteins in a gel that takes advantage of the fact that overall charge on the molecule of interest is a function of the pH of its surroundings. Living eukaryotic cells perform isoelectric focussing of proteins.
It is also called as Gamma Globulin Electrophoresis or Immunoglobulin Electrophorsis, is a method of determining the blood levels of three major immunoglobulins: IgM, IgG, IgA.it is a powerful analytical technique with high resolving power as it combines separation of antigens by electrophoresis with immuno diffusion against an antiserum. The increased resolution is of benefit in the immunological examination of serum proteins. This method aids in the diagnosis and evaluation of the therapeutic response in many disease states affecting the immune system.
It is a technique in analytical chemistry used to separate charged particles. It is a further development of electrophoresis. It is a powerful separation technique using discontinuous electrical field to create sharp boundaries between the sample constituents.
In this technique the sample is introduced between a fast leading electrolyte and a slow terminating electrolyte. After application of an electric potential a low electrical field is created in the leading electrolyte and a high electrical field in the terminating electrolyte. The pH at sample level is determined by the counter ion in the leading electrolyte that migrate in the opposite direction. In the first stage the sample constituents migrate at different speeds and start to separate from each other. The faster constituents will create a lower electrical field in the leading part of the sample zone and vice versa.
11. Serum Protein Electrophoresis:
In the bottom plot, a sharp spike has replaced a diffuse hump in the gamma region, because normal gamma globulins are decreased and large amounts of a single monoclonal immunoglobulins have taken their place. Because the protein is monoclonal, each molecule has identical electrophoretic qualities that move it to the same place in the electric field, creating a narrow, intense band or spike. Discovery of an M-Component suggests the presence of multiple myeloma, monoclonal gammopathy of undetermined significance, Waidenstrom’s macroglobulinemia, other lymph proliferative disease, or primary systemic amyloidosis.
12. Pulsed Field Gel Electrophoresis (PFGE):
It is a technique used for the separation of large DNA molecules by applying an electric field that periodically changes direction to a gel matrix.
The theory behind why PFGE works pertains to the mobility of larger DNA fragments. While in general small fragments can find their way through the matrix more easily than large DNA fragments, a threshold length exists above 30-50 kb where all large fragments will run at the same rate and appear in a gel as a single large diffuse band.
Electrophoresis is mainly used for the separation of ionisable substances by using buffers of different pH and ionic strength.
* Separation of amino acids (into acidic or basic or zwitter ionic type)
* The type of protein and the percentage of each component can be determined using densitometer.
* Separation of lipoproteins in serum (in case of hyperlipidemia).
* Separation of enzymes from blood.
* For the separation of ions containing same electrophoretic mobility, Isotachophoresis is used to separate the ions by gradient pH application.
* Dielectrophoresis can be used to manipulate, transport, separate and sort different types of particles.
* Separation of proteins in serum (into albumin, α1, α2, β1, β2 and Gamma globulins).
* Separation of alkaloids and antibiotics in different samples can be carried out.
* For DNA separation and analysis.
* Vaccine analysis
Electrophoresis is laboratory separation technique which is widely used in biochemistry, biotechnology and analytical laboratories. It is an effective separation technique with the exemption of ‘electro non conductible’ and ‘non-ionic substances’. Now a days it is extensively used for separation and analysis of nucleic acids like DNA and RNA.
1. Lyklema.J (1995), Fundamentals of Interface and Colloid Science, vol-2, P-3.208.
2. Hunter.R.J.(1989), Foundations of Colloid Science, Oxford University Press.
3. Dukhin.S.S; B.V.Derjaguin (1947), electrokinetic phenomena, J.Wiley and Sons.
4. Russel.W.B; D.A.Saville and W.R.Schowalter (1989), Colloidal Dispersions, Cambridge University Press.
5. Kruyt.H.R.(1952), Colloid Science, Volume-1, Irreversible Systems, Elsevier.
6. Dukhin.S.S; P.J.GOEDGE (2002), Ultra Sound for Characterising Colloids, Elsevier.
7. Reuss.F.F (1809), Mem.Soc.Imperiale Naturalistes de Moscow 2:327.
8. Von Smoluchowski.M, (1903), Bull. Int. Acad.sci. cracovie-184.
9. Huckel.E (1924), Physic.Z. 25:204.
10. Overbeek.J.Th.g (1943). Koll.bith: 287.
11. Booth.F (1948), Nature 161:83. Bibcode (1948) Nature-161...83B.doi: 10.1038/161083a0.
12. Dukhin.S.S; N.M.Semenikhin (1970), Khol.zhur: 32-366.
13. O’Brein.R.W; L.R.White (1978).j.chem.soc.faraday Trans. 2 (74): 1607.
14. Knecht et al.(2008).J.Col.Int.Sc.318: 477.
15. Voet and Voet (1990), Biochemistry. John Wiley & Sons.
16. Barz.D.P.J; P. Ehrhard (2005) “Model and Verification of Electrokinetic Flow and Transport in a Micro-Electrophorsis Device”. Lab Chip 5:949-958.
17. Shim. J; P. Dutta and C.F. ivory (2007). “modelling and Simulation of IEF in 2-D Microgeometrics”. Electrophoresis 28: 527-586.
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