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Serum proteins are separated in an electric field according to their size,
shape, and electric charge. The separation is performed on agarose
gels. The proteins are visualized by staining with acid blue and the
intensity of staining is quantitated by densitometry (Helena Quick Scan 2000).
Multiplying by the serum total protein converts the percentage of protein in
each fraction into serum concentration. (Helena SPIFE 3000 Instruction
Manual; Package insert: Helena SPIFE SPE Vis Gel, 2001;
Kyle RA, Katzmann JA, Lust JA, Dispenzieri A: Clinical indications and
applications of electrophoresis and immunofixation. In Manual of Clinical
Laboratory Immunology. 6th edition. Edited by NR Rose, et al.
Washington, DC, ASM Press, 2002 pp 71-91)

