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Electrophoretic Mobility (μ)

Definition

Velocity of a charged particle per unit electric field, μ = v/E. Depends on charge, size, shape and the viscosity of the support medium.

Symbol
μ
Formula
μ = v/E
Depends on
Charge, size, shape, medium viscosity
Field
Electrophoresis

Common questions

Why do two molecules with the same net charge sometimes have different electrophoretic mobility?+

Mobility also depends on the size and shape of the molecule and the friction it experiences moving through the support medium, so a smaller or more compact molecule can move faster than a larger one even when their net charge is identical.

How is electrophoretic mobility used practically in forensic serology or DNA work?+

Differences in mobility separate proteins, isoenzymes, or nucleic acid fragments into distinct bands or zones on a gel, and comparing the mobility pattern of a questioned sample against a known reference is the basis for typing and identification in electrophoretic methods.

Related terms

Agarose
Polysaccharide gel from seaweed. Large pore size, used for nucleic acids and large proteins. Standard for DNA submarine gels.
Capillary Electrophoresis (CE)
A separation technique that resolves DNA fragments by size through a polymer-filled glass capillary under an applied electric field. Single-base resolution is...
IEF (Isoelectric Focusing)
Electrophoresis across an immobilised pH gradient. Each protein migrates until it reaches its pI and stops. Very high resolution; used in haemoglobin...
Immunoelectrophoresis
A two-step technique: proteins are first separated by electrophoresis in agar gel, then antiserum diffuses from a parallel trough and forms precipitin...
Isoelectric Point (pI)
pH at which a molecule (usually a protein) carries zero net charge and stops migrating. The basis of isoelectric focusing (IEF).
Polyacrylamide (PAGE)
Cross-linked synthetic gel with tunable, smaller pore size. Used for proteins and small DNA fragments.
Precipitin Arc
Curved line of antigen-antibody precipitate that forms at equivalence in immunoelectrophoresis. Shape and position identify the antigen.
SDS-PAGE
PAGE run with sodium dodecyl sulphate. SDS coats proteins with uniform negative charge, so separation is by molecular weight alone.

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