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Urine samples collected from Ate1-deficient mice were pooled and compared with pooled urine from Ate1-containing mice.
Cells from three mice were pooled for each shRNA.
Injected DRGs from 2 mice were pooled together.
Splenocytes from 5 to 6 Cicf/f mice or 3 to 4 Cicf/fCd4-Cre mice were pooled and subjected to cell sorting.
Macrophages of normal mice were pooled and incubated with lemongrass essential oil (similar components to L. liversidgei chemotype II) at 37°C for 24 h.
Lymph nodes from two mice were pooled for TCR repertoire analyzes.
Plasma from 5 mice with cancer and 5 control mice were pooled for further analysis.
Total RNA from 3 mice were pooled and one microarray was used for each pool.
For each group, tissues from five mice were pooled before RNA extraction.
The same RNA amounts from 2 mice were pooled into one sample.
Preimmune serum samples or serum samples after the third immunization of individual mice were pooled for each group.
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