Fig. 1.
Fig. 1. Schematic illustration of the localization of the primers for genotyping of C807T dimorphism (top). Allele-specific amplification (PCR-SSP) was performed with intronic common sense primer (92V) and antisense primers C807 or T807 (96C or 96T). Representative results of GPIa genotypes determined by PCR-SSP of three individuals: homozygous CC (lanes 2), heterozygous CT (lanes 3), and homozygous TT (lanes 4). Genomic DNA were amplified using specific primer for C807 (left panel) or for T807 allele (right panel) and were analyzed on 1.8% agarose gel electrophoresis. The GPIa bands represent the allele-specific PCR product and the HGH bands the internal control. DNA size standards V (Boehringer Mannheim) were used as standard (lanes 1). Negative controls are shown in lanes 5.

Schematic illustration of the localization of the primers for genotyping of C807T dimorphism (top). Allele-specific amplification (PCR-SSP) was performed with intronic common sense primer (92V) and antisense primers C807 or T807 (96C or 96T). Representative results of GPIa genotypes determined by PCR-SSP of three individuals: homozygous CC (lanes 2), heterozygous CT (lanes 3), and homozygous TT (lanes 4). Genomic DNA were amplified using specific primer for C807 (left panel) or for T807 allele (right panel) and were analyzed on 1.8% agarose gel electrophoresis. The GPIa bands represent the allele-specific PCR product and the HGH bands the internal control. DNA size standards V (Boehringer Mannheim) were used as standard (lanes 1). Negative controls are shown in lanes 5.

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