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Exact(9)
The antioxidant status of the plasma from AH and AC exposed mice was assayed with an antioxidant reductive capacity assay (NWK-ARC01; Northwest Life Science Specialties, Vancouver, WA).
In order to discard the possible effect of mouse blood present in the trypomastigote suspension, blood from T. cruzi uninfected mice was assayed in parallel in all co-infection experiments.
The expression of eGFP in tissues of F1 transgenic mice was assayed by confocal microscopy (LSM 510, Zeiss, Oberkochen, Germany).
Spontaneous locomotor activity of wild-type and Id2−/− mice was assayed using the open-field test (Walsh and Cummins, 1976).
The gene expression profile of the gastric fundus of wild type and W/W V mice was assayed by murine microarray analysis displaying a total of 8734 elements.
The concentration of glutathione (GSH) in testis of control and all treated groups of mice was assayed by the method of Ellman (1959).
Similar(51)
b PLs from saline and S. pneumoniae infected WT and PAI-1−/− mice were assayed for plasmin activity.
For HFD experiments, mice were assayed after 20 to 26 weeks on HFD.
Intraperitoneal macrophages from WT and CD36−/− mice were assayed for capacity to efflux CE to HDL.
BKS db/+ and db/db mice were assayed at 6 weeks and at 10- and 14-weeks of age.
Sera of individual mice were assayed for the presence of gp63-specific IgG1, IgG2a antibodies using enzyme-linked immunosorbent assay (ELISA) as described earlier [29].
Related(20)
mice was estimated
mice was investigated
mice was analysed
mice was quantified
mice was sampled
individuals was assayed
mice was evaluated
mice was corroborated
mice was reassessed
mice was substantiated
mice was ascertained
mice was measured
specimens was assayed
rat was assayed
mice was deprived
mice was focused
mice was maintained
mice was used
mice was digested
mice was colored
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