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High Sensitivity of Laser-Induced Fluorescence Detection in Capillary Gel Electrophoresis for Accurate Apolipoprotein E Genotyping
Author(s) -
Alexandra Schlenck,
Karin Bohnet,
Dominique Aguillon,
C. Lafaurie,
Gérard Siest,
Sophie VisvikisSiest
Publication year - 1997
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/97224rr03
Subject(s) - capillary electrophoresis , genotyping , laser induced fluorescence , fluorescence , gel electrophoresis , chromatography , microbiology and biotechnology , sensitivity (control systems) , chemistry , biology , genetics , genotype , gene , optics , physics , electronic engineering , engineering
Human apolipoprotein E (apoE) is a product of a polymorphic gene. In the general population, it shows two major mutations, which lead to the appearance of three common alleles encoding for three protein isoforms. This polymorphism is important in the regulation of lipid metabolism. Accurate apoE phenotyping or genotyping has become essential in clinical laboratories, since the epsilon 4 allele has been associated with cardiovascular and Alzheimer's diseases. Endonuclease restriction isotyping, followed by slab gel electrophoresis, is a rapid and convenient method for the investigation of common apoE genotypes. However, during the large-scale apoE genotyping of the STANISLAS cohort, we were confronted with a partial lack of sensitivity and resolution power of this traditional method, which sometimes leads to the misclassification of the genotypes epsilon 2/2 and epsilon 3/2. We have overcome this difficulty by separating the restriction fragments with capillary gel electrophoresis linked to laser-induced fluorescence detection. The baseline resolution was 2 bp, and the sensitivity limit attainable was similar to that by radioactive detection. The distinction between the epsilon 3/2 and the epsilon 2/2 genotypes became unequivocal, even when only low amounts of DNA were available for amplification.

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