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. Author manuscript; available in PMC: 2010 Jan 15.
Published in final edited form as: J Neurol Sci. 2008 Nov 8;276(1-2):133–137. doi: 10.1016/j.jns.2008.09.037

Fig. 2.

Fig. 2

Agarose gel electrophoretic analysis of PCR amplification for the shi and WT alleles, displayed as 380- and 169-bp amplification products, respectively, from brain genomic DNA of shi/shi (Lane 2), B6C3F1 (Lane 3), Ini1+/− (Lane 4), shi/shi; MBP/MBP (Lane 5), and the 5 “rescued” shi chimeric (1, 2, 3, 4 and 5; Lanes 6 – 10) mice. The size of the amplification products was determined by reference to the 100-bp DNA ladder (Lanes 1 and 12). For negative control, water was used in place of genomic DNA as template (Lane 11).