Sentence examples for mice were adjusted from inspiring English sources

For LPS stimulation, the splenocytes from 1-month old MRL-lpr mice were adjusted to 5×106 cells/ml, plated in 24-well plate, and then activated for 24 hrs by adding equal volumes of media containing LPS (Sigma, 1000 ng/ml) to seeded cells (final concentration at 500 ng/ml).

The fixation times for embryonic/perinatal mice were adjusted as follows: E13.5 E18.5, 1 hour; postnatal day 3 (P3), 2 hours; P10, 4 hours; and P21, 10 hours.

Thus, the individual gene expression level in infected mice was adjusted for the gene expression level in uninfected mice for each mouse strain.

The head of the mouse was adjusted on the nose bar so that bregma and lambda were at level height.

Preliminary tests were performed to determine the volume of oil remaining in the pipette tip after dosing, and the total volume per mouse was adjusted to allow for this remaining amount.

To counteract overregularization and loss of detail in case of the attenuation CT, the noise power spectrum of the three mice datasets were adjusted by weighting iterative reconstruction and conventional filtered back-projection reconstruction (with Ram-Lak filter) with 0.75 and 0.25 respectively.

Isolated mouse neutrophils were adjusted to 5×106 cells/ml and incubated with HBSS (neg ctrl), 20 ng/ml LPS (pos ctrl), norepinephrine (10−10 M) or epinephrine (10−10 M) for 4 hrs at 37°C/5%CO2.

The images of lacZ staining of the mouse brain sections were adjusted for brightness and contrast using Photoshop, but all images for the same construct (test and control samples) received the same adjustments.

Amounts of liposomal formulations injected were adjusted for each mouse to receive 15  μg of coupled Tc-ErbB2 peptide per injection.

Counts were adjusted for the higher HDL levels in CD36−/− mice.

All doses were adjusted according to the individual weight of each mouse.