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. 2005 Apr;43(4):1940-3.
doi: 10.1128/JCM.43.4.1940-1943.2005.

Multiplex PCR for typing strains of Toxoplasma gondii

Affiliations

Multiplex PCR for typing strains of Toxoplasma gondii

Daniel Ajzenberg et al. J Clin Microbiol. 2005 Apr.

Abstract

A multiplex PCR assay was designed for multilocus strain typing of Toxoplasma gondii based on length polymorphism of five microsatellite markers. Eight T. gondii strains already sequenced at these five markers were used as control isolates. This method is simple, rapid, reproducible, and adapted to a large set of isolates.

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Figures

FIG. 1.
FIG. 1.
Agarose gel electrophoresis of multiplex PCR amplification products with control isolates. Lanes: 1, BK; 2, ME49; 3, NED; 4, BOU; 5, DEG; 6, RMS-2001-MAU; 7, PSP-2003-KOM; 8, GUY-2002-MAT; V, molecular size markers.
FIG. 2.
FIG. 2.
Electrophoresis of multiplex PCR amplification products from a type II isolate (ME49) with an automatic sequencer by using GeneScan software. The x axis indicates a size fragment scale (in base pairs). The y axis indicates a peak height scale corresponding to the fluorescence intensity of detected peaks. Size fragments of GeneScan size standard ROX 500 are indicated between 75 and 500 bp.

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