Sentence examples for mouse embryo sections from inspiring English sources

To characterize the expression of mATX3 in the developing muscle, we performed double immunofluorescence labeling for mATX3 and myogenic markers in mouse embryo sections from E9.5 to E18.5.

We carried out IHC of mouse embryo sections by double-staining TRIM59.

Immunohistochemistry was also performed on 13.5 dpc wild-type and Satb2-null mouse embryo sections (19).

As a prelude to the phenotypic characterization, we investigated SNRK protein expression using immunofluorescence (IF) microscopy technique on mouse embryo sections.

Sections were double-stained with pan-cytokeratin antibody with FICT (Sigma, St .Louis, Missouri, USA), and the stained mouse embryo sections were visualised using a Carl Zeiss (Oberkochen, Germany) confocal microscope by the LSM Image program.

In analysis of the full experimental set, for any given antibody all sections were stained at the same time so as to be directly comparable, and a normal mouse embryo section was included as a positive control.

Staining intensity was scored on a scale of 0-4+, using the mouse embryo control section as a reference standard for each run.

For samples after 6 weeks of chemopreventive treatment, staining intensity was scored on a scale of 0 4+, using the mouse embryo control section as a reference standard for each run.

Immunoperoxidase labelling of nestin or GR on consecutive sections of mouse embryo heads (E14.5) demonstrated strong nestin and GR signals in neural cells lining the third ventricle (Figure 1, A, B, and C) and in muscle cells adjacent to a hair follicle (Figure 1, A, D, and E).

We found that endogenous palladin can be detected in the nucleus of cultured rat aortic SMCs (Fig. 7A), A404 cells (data not shown), SMCs and endothelial cells in sections of mouse embryo E11.5 blood vessels, and human coronary vessels from patients with atherosclerotic disease (Figure S2).

To address these limitations, tissue based color targets have been proposed such as a section of mouse embryo stained in a standard way.