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For each probe set, 50 plasma cells (if possible) were scored and the result for each probe was reported.
Representative sections for each probe are shown (wild-type animals, n=6).
Representative sections for each probe are shown (wild-type zebrafish, n=6 and mouse, n=4).
For each probe to be screened, all putative ligands were assayed in parallel.
A total of 200 interphase cells were analysed for each probe.
Spot intensities for each probe were calculated by subtracting median local background from median local foreground for each spot.
A linear fit in the range of 0 100 cytoplasmic spots is applied to extract CU for each probe set.
Figure 5 Doppler shift arrangement for each probe antenna.
For each probe (which, at run-time, is continuously delivering information to the controller under test), we apply a single change for each probe data sample.
Three microarrays were performed for each probe.
One hundred cells were assessed for each probe.
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