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Figure 9 Scatter profile.
The figure shows the fit of the scatter profile obtained from the setup shown in Figure 8.
The effective attenuation coefficient μ ∧ was obtained by fitting the scatter profile along a tank filled with water and placed on a MEGP collimator with a90Y point source placed on one side of the tank (Figure 8).
The effective attenuation coefficient μ ∧ was obtained by fitting the scatter profile along a tank filled with water and placed on a MEGP collimator, with a90Y point source placed on one side of the tank (see Appendix 1).
and further corroborated with the forward scatter vs. side scatter profile.
The platelet population as identified by forward and side scatter profile.
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Lymphocytes were gated on forward and side scatter profiles.
Side and forward scatter profiles were used to eliminate cell doublets.
Dead cells were excluded from analysis based on forward and side scatter profiles.
Forward and side scatter profiles were used to gate on the lymphocyte population.
3T3 cells were distinguished from NKT or CD4+ Th cells by their distinctive larger forward and side scatter profiles.
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