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Aorta from each mouse was divided into 4 rings of 2-mm length.
To describe the regional ICG pharmacokinetics in vivo, the rear half of a mouse was divided into three compartments: the trunk, the normal hindlimb, and the ischemic hindlimb.
Each strain of mouse was divided equally into two experimental groups, which included 1) Control: fed a control diet (10% kcal fat, Research Diets Inc., D12450B), or 2) High-fat: fed a high-fat diet (60% kcal fat, Research Diets Inc., D12492).
The average number of LP cells and IECs for each TM IEC C1galt1 −/− mouse was divided by the average number obtained for each WT, and converted to percentage.
For each gene, the level of gene expression in each sample taken from an infected mouse was divided by the median of gene expression levels in samples taken from three uninfected mice.
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The original sample of 60 mice was divided into two independent biological replications of 30.
The cohort of SCCVII tumour-bearing mice was divided into groups for various treatments.
Adult mice were divided into three groups.
Swiss albino mice were divided uniformly into seven different groups.
Every ten mice were divided into a group.
Every ten ICR female mice were divided into one group.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com