196
Participants
Start Date
August 1, 2018
Primary Completion Date
October 6, 2019
Study Completion Date
October 6, 2019
Genetic analysis
he real-time PCR amplification was performed in a final volume of 20μL reaction mixture, including 10 ng of genomic DNA, 5 µL of TaqMan® Universal PCR Master Mix, and 0.5 µL of 40X TaqMan® assay. Thermal cycling conditions were as follows: initial denaturation at 94℃ for 3 min, 40 cycles of 94℃ for 15 s, and 60°C for 1 min. The Rotor-Gene Q Series Software Version Q 2.3.1 (Rotor-Gene Q Series, Ziagen) was used for allelic discrimination.
Omer Gokhan Doluoglu, Ankara
Saglik Bilimleri Universitesi
OTHER