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. Author manuscript; available in PMC: 2012 Mar 14.
Published in final edited form as: Cell Signal. 2011 Jun 15;23(10):1617–1624. doi: 10.1016/j.cellsig.2011.05.015

Fig. 2.

Fig. 2

Ability of the Gγ2/Gγ15 subunit chimeras to reverse gng2-SaaX-induced PGC migration defects. Embryos were injected with 50 pg of gng2-SaaX(nos) mRNA (scored when injected alone on the leftmost in red) and received a subsequent injection with 100, 200, or 300 pg of the gng15/gng2 chimeric Gγ mRNA (A). The ectopic PGC score of larvae injected with 100–300 pg/embryo of the chimeric Gγ-WT(nos) mRNA alone is shown in (B). Each concentration is summarized from 2 to 5 experiments with a minimum of 20 larvae scored for the number of ectopic PGCs at 24 hpf. (Ectopic PGC migration score is expressed as mean +/− S.D.) An ectopic score of 0 represents wild type migration; 1=5–20% ectopic; 2=21–40% ectopic; 3=41–60% ectopic; 4=61– 80% ectopic; 5=81–100% ectopic PGCs. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)