Electrophoresis

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[[SDS polyacrylamide-gel electrophoresis|Electrophoresis]] is used as a method of separating [[DNA|DNA]] according to size, using a porous gel as a filter (usually [[Polyacrylamide|polyacylamide]] gels are used). By applying an electric current, the [[Molecule|molecules]] of [[DNA|DNA]] are made to move through the gel towards the positive electrode ([[Anode|anode]]), with the smaller or more compact strands travelling the fastest. This produces distinct bands of [[DNA|DNA]], which can be identified by comparing with a known [[DNA|DNA]] sample 'ladder' run simultaeously. Any molecule with a net charge, such as proteins, can also be seperated using this technique.<br>  
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[[SDS polyacrylamide-gel electrophoresis|Electrophoresis]] is used as a method of separating [[DNA|DNA]] according to size, using a porous gel as a filter (usually [[Polyacrylamide|polyacylamide]] gels are used). There are two separate portions presence across the gel, stacking gel and resolving gel. The stacking gel consists low percentage of polyacrylamide where bigger molecule tends to move slower. While the resolving gel contains higher percentage of polyacrylamide, which the smaller molecule can move faster and further in distance. &nbsp;By applying an electric current, the [[Molecule|molecules]] of [[DNA|DNA]] are made to move through the gel towards the positive electrode ([[Anode|anode]]), with the smaller or more compact strands travelling the fastest. This produces distinct bands of [[DNA|DNA]], which can be identified by comparing with a known [[DNA|DNA]] sample 'ladder' run simultaeously. Any molecule with a net charge, such as proteins, can also be seperated using this technique.<br>  
  
 
The mobility of charges molecules are influenced by:  
 
The mobility of charges molecules are influenced by:  
  
*Net Charge of molecule. Negitive charged molecules move towards the positive end of the electrode (anode) while positive charged molecule move towards the negitive end of electrode (cathode).&nbsp;
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*Net Charge of molecule. Negitive charged molecules move towards the positive end of the electrode (anode) while positive charged molecule move towards the negitive end of electrode (cathode).&nbsp;  
*Size of [[molecule|molecule]]
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*Size of [[Molecule|molecule]]  
*Shape
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*Shape  
 
*Electrical field strength applied<ref>Rob Reed et al (2013) Practical Skills in Biomolecular Sciences 4th edition, Essex, Pearson Education Limited</ref>
 
*Electrical field strength applied<ref>Rob Reed et al (2013) Practical Skills in Biomolecular Sciences 4th edition, Essex, Pearson Education Limited</ref>
  
=== References ===
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=== References ===
  
 
<references />
 
<references />

Revision as of 15:28, 9 October 2014

Electrophoresis is used as a method of separating DNA according to size, using a porous gel as a filter (usually polyacylamide gels are used). There are two separate portions presence across the gel, stacking gel and resolving gel. The stacking gel consists low percentage of polyacrylamide where bigger molecule tends to move slower. While the resolving gel contains higher percentage of polyacrylamide, which the smaller molecule can move faster and further in distance.  By applying an electric current, the molecules of DNA are made to move through the gel towards the positive electrode (anode), with the smaller or more compact strands travelling the fastest. This produces distinct bands of DNA, which can be identified by comparing with a known DNA sample 'ladder' run simultaeously. Any molecule with a net charge, such as proteins, can also be seperated using this technique.

The mobility of charges molecules are influenced by:

References

  1. Rob Reed et al (2013) Practical Skills in Biomolecular Sciences 4th edition, Essex, Pearson Education Limited
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