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[DOI] [PMC free article] [PubMed] [Google Scholar] Prabakaran S, Swatton JE, Ryan MM, Huffaker SJ, Huang JT, Griffin JL, Wayland M, Freeman T, Dudbridge F, Lilley KS, Karp NA, Hester S, Tkachev D, Mimmack ML, Yolken RH, Webster MJ, Torrey EF, Bahn S

The gel, placed in a tank with 1x TAE buffer, was loaded with the DNA mixture (25l sample + 5l 6x loading dye) and 5l ladder, then run at 100V for 50 minutes