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. 2013 Jan;99(1):76–85. doi: 10.1016/j.fertnstert.2012.08.035

Table 2.

Expression of microinjected cRNA encoding luciferase-tagged wild-type phospholipase Cζ (PLCζ) mutants PLCζH233L and PLCζH398P in unfertilized mouse eggs.

PLCζ-luciferase injected Ca2+oscillations (spikes/2 h) Peak luminescence (cps) Time to 1st spike (min) Luminescence at 1st spike (cps)
PLCζWT 9.02 ± 0.037 0.42 ± 0.020 ∼25 0.07 ± 0.005
PLCζH233L 2.84 ± 0.076 0.40 ± 0.050 ∼190 0.34 ± 0.040
PLCζH398P 0.39 ± 0.020

Note: Values are mean ± standard error of the mean. The Ca2+ oscillation-inducing activity (Ca2+ spike number in 2 hours; time to first spike) and the simultaneously-measured PLCζ-luciferase fusion protein luminescence levels (peak luminescence; luminescence at first spike) are summarized for mouse eggs that had been microinjected, as described in Materials and Methods, with cRNA encoding one of the following human PLCζ-luciferase constructs: wild-type PLCζ, the PLCζH233L or PLCζH398P mutant (see Fig. 4B). cps = counts per second.