Sentence examples for mouse skin sections from inspiring English sources

H&E-stained mouse skin sections were used to quantify the presence of apoptotic keratinocytes.

To analyze, Ran, Raph1, Lasp1 and p63 expression patterns during wound healing, immunohistochemical staining was performed on lesional mouse skin sections collected 3 days post wounding.

Immunohistochemistry showed similar patterns of expression for ADH and ALDH in both strains of mouse skin sections, with localization predominantly in the epidermis, sebaceous glands, and hair follicles.

To exclude the possibility that GIRK channels are only detectable at peripheral nerve terminals, we also immunostained mouse skin sections with GIRK2 antibodies and the neuronal marker IB4.

Cells positive for α-SMA in mouse skin sections were detected by incubation with monoclonal anti-α-SMA antibody (clone 1A4; Sigma-Aldrich, Saint-Quentin Fallavier, France) diluted 1 1,000 for 3 hours at room temperature.

Eight different high-power fields from each mouse skin section were evaluated for inflammatory infiltrate by two independent examiners blinded to the treatment.

Briefly, 10 20 random measurements along the skin from at least five mice (three skin sections per mice) per injected group were considered.

In accordance with an unaltered epidermal thickness, immunofluorescence (IF) staining of mouse back skin sections revealed comparable expression of the proliferation marker Ki67 in Cre-deficient control, Hdac1Δ/Δep and Hdac2Δ/Δep mice (Supplementary Figures S1E and F).

Histological examination of mouse back skin sections was carried out at different time points from day 3 through day 16 (Figures 4A 4P).

To visualize cross-sections of mouse skin, whole skin tissue was embedded in O.C.T. compound (Tissue-Tek), and 10 µm skin sections were cut on a Leica Cryostat.

To analyze miR-203 expression in injured skin, in situ hybridizations were performed on sections of mouse skin samples collected at 3 and 5 days post wounding.