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Two phase microstructure with matrix having good distribution of CNT and CNT rich clusters was observed.
IO encapsulation was however unsuccessful, and a phase separation between the polymer and the IO clusters was observed.
A considerable influence of oxygen addition on the formation of clusters was observed even at oxygen-to-argon admixture levels of the order of 1 1000.
In the latter case the precipitation of Nb-rich clusters was observed, and atom probe tomography revealed them to be ∼85% Fe.
In the absence of laminin-1, ß-DG labelling was largely diffuse at the cell surface (Fig. 1A), however in the presence of laminina dose-dependent response both in the number and area of the clusters was observed reaching a plateau at 20 nM of laminin-1as previously reported in Muller glial cells (Fig. 1A C; 21A C
The heterogeneous p75 reactivity within neuroepithelial clusters was observed using three different antibodies; rabbit polyclonal serum and two mouse monoclonal antibodies (including one directly conjugated, previously used for isolation of human NCSCs [16].) For HNK-1 staining, we used the same monoclonal antibody staining conditions as previously reported [15].
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Some clusters were observed in multiple years.
Significant differences in the number of growing clusters were observed among the conditions.
No distinct clusters were observed among the CRM_B samples from the two time points (Fig. 5c).
FAK clusters are observed to associate with actin filaments (Fig. 5; Supplementary Movie S16).
Two evolving ways of impact clusters are observed.
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