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. 2010 Jul 14;9(11):2369–2390. doi: 10.1074/mcp.M110.001370

Fig. 3.

Fig. 3.

Gel electropherograms of RT-PCR products generated from gene-specific primers for exendin-1 (A) and exendin-2 (B) are shown. Lane 1, standard DNA ladder, each band representing 100-base pair increments; lane 2, RT-PCR product from the venom library of H. suspectum; lane 3, non-template control; lane 4, RT-PCR from venom libraries of Mexican beaded lizard (H. horridum). C, gel electropherogram of RT-PCR products generated from kallikrein gene-specific primers. Lane M, standard DNA ladder, each band representing 100-base pair increments; lane 1, RT-PCR product from the venom library of H. horridum with primers designed from H. suspectum kallikrein sequence EU790962 obtained in this study; lane 2, non-template control; lane 3, RT-PCR from venom libraries of H. horridum with primers designed from the H. horridum kallikrein sequence P43685 reported previously; lane 4, non-template control.