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. Author manuscript; available in PMC: 2010 Apr 1.
Published in final edited form as: Psychiatr Genet. 2009 Apr;19(2):72–82. doi: 10.1097/YPG.0b013e3283208091

Fig. 7. Use of RMS-prepared DNA for HTTLPR LA/LG screening.

Fig. 7

HTTLPR genotyping PCR was carried out on DNA samples generated by RMS as described in the text. A volume of 9μl of sample previously determined to be l/l genotype was used. PCR was followed by overnight (16hr) digestion of reaction products with HpaII restriction enzyme. Both full and partial digestion products were present. Sample was LA/LA, since none of the potential LG digestion products (dashed-line arrows) appeared.