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. 2009 Mar 17;10(4):275–287. doi: 10.1007/s10048-009-0183-3

Fig. 4.

Fig. 4

Transcription activation-Gal4 reporter assay using full-length clones (1–754) for the wild-type (filled square) and A335V (filled diamond) mutation at different protein concentrations. The highest activation at 5 µg was found for a Gal-(1–715) clone (filled triangle, left side top). The empty vector pGLMRG5 was used as control (filled circle, left side down)