Sentence examples for rat tissue sections from inspiring English sources

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4H1 binds fixed mouse BChE in transfected mammalian cells (figure 2C) and rat tissue sections (figure 2D).

Frozen human and rat tissue sections were homogenized in suspension buffer as described (Eastwood et al., 2001b).

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For quantification of perivascular Aqp4 in rat tissues, sections were double-labeled for Aqp4 and RECA-1 and three epifluorescence images were obtained at random locations within each ROI using a 20x air objective.

For AF imaging and for each kind of histochemical procedure, images shown in the respective figures were chosen as representatives of the patterns obtained from each of the control or MCD diet administered rats (6 tissue sections per rat).

No immune reactivity was observed in immunohistochemistry studies performed to show potential infiltrating CD3, CD4 or CD8+ T cells, CD19+ B cells, and CD11b/c+ neutrophils/macrophages (Additional file 2: Table S2), while the control rat spleen tissue sections showed abundant reactivity with these markers (not shown).

Primer sequences are listed in Table 4. Paraffin-embedded, paraformaldehyde-fixed rat atrial tissue sections were deparaffinized in toluene and hydrated in a graded alcohol series.

To determine the neuron differentiation of hMSCs in rat brain, tissue sections from exogenous implanted bisbenzimide-labelled hMSCs (blue fluorescence) were stained with specific primary antibodies (1 300) against PPARγ and a neuron specific marker, MAP2.

Furthermore, the Mann–Whitney U test (for the hydrogel digestion experiments performed via microwave and oven) and Kruskal Wallis test (for all the digestions carried out using the 1 mm rat brain tissue sections) were applied to the number of protein groups and the number of distinct peptides in order to find possible statistical differences between groups.

Negative (without lectin or primary antibody) and positive (known rat or human tissue sections) controls were also tested.

The localization of 18F radioactivity in rat and human pancreatic tissue sections was investigated with autoradiography.

Immunohistochemical labeling of augurin and in situ hybridization of Ecrg4 in mouse, rat and human brain tissue sections showed that protein and gene expression localize in large part, albeit not exclusively, to CP and ependymal epithelial cells.

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