Sentence examples for fixed mice from inspiring English sources

For analysis of neuromuscular denervation medial gastrocnemius muscle from 4% paraformaldehyde fixed mice were dissected, embedded into gelatin blocks and sectioned at 80 μm with a freezing microtome [ 22].

In addition, diffusion-weighted images of a fixed mouse spinal cord illustrated the capability of this coil for quantitative imaging of tissue microstructure.

Excitingly, p-FE enables one-photon based, three-dimensional (3D) confocal imaging of vasculatures in fixed mouse brain tissue with a layer-by-layer imaging depth up to ~1.3 mm and sub-10 µm high spatial resolution.

Fluorescence from Cu2O nanocubes was also observed to be significantly brighter than the auto-fluorescence from a fixed mouse cumulus-oocyte complex and highly photostable compared to commercially available organic fluorescent materials.

Owing to the high QY of p-FE, we succeeded in using confocal imaging ex vivo to decipher 3D vasculatures in fixed mouse brain tissue immersed in glycerol through collection of fluorescence emitting above 1100 nm under the excitation of a tightly focused 785 nm laser (see Method for details).

The bright nanofluorophore enables 3D confocal layer-by-layer imaging of formalin fixed mouse brain tissue to resolve vessels with apparent widths of ~5 7 µm in diameter at imaging depth up to ~1.3 mm in the NIR-II window, which is the deepest 3D fluorescence microscopy of brain tissues using the one-photon fluorescence technique.

Immunohistochemistry was performed using OCT-embedded, 4um thick acetone fixed mouse tissue sections.

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

For immunohistochemistry with the GFP antibody (Table 2), PFA fixed mouse sections were deparaffinized after which endogenous peroxidases were blocked with methanol/0.3% H2O2.

A pull-down reagent comprised of the Pak1-RBD was used as an affinity probe in immunohistochemistry experiments to demonstrate Rac activation in FFPE fixed mouse mammary tumors driven by Neu and TGFβ1 [26].

Immunohistochemical analyses of fixed mouse lenses extend these findings.