Sentence examples for murine kidney sections from inspiring English sources

TEM and co-localization IEM of murine kidney sections were performed exactly as described by Kalaaji et al. [36], [46].

To achieve profiling and demonstrate coarse tissue-specific MS measurement of the observable N-glycan population in FFPE tissue, four replicate FFPE murine kidney tissue sections were treated with antigen retrieval, and large droplets of glycerol-free PNGase F were printed onto the sections and incubated overnight at 37 °C.

For murine kidney samples, serial sections (thickness of the sections: 2 µm) were done and processed by hematoxylin-eosin and HIF-1α staining.

Sections of FFPE murine kidney tissue (N = 3) were manually microdissected, treated with antigen retrieval, and incubated overnight with PNGase F (two of three sections).

In the present study, we outline an improved automated sample preparation method for N-glycan MALDI imaging, which uses in situ PNGase F-mediated release and measurement of N-linked glycans from sections of formalin-fixed murine kidney.

Of the 251 putative anchor genes selected, 200 were analysed using high resolution section in situ hybridisation (SISH) of paraffin-embedded E15.5 murine kidney.

(h) H&E-stained kidney sections showing glomerulonephritis in the 12-month-old Cicf/fVav1-Cre mice.

(e) H&E-stained kidney sections showing glomerulonephritis in 14.5-month-old Cicf/fCd4-Cre mice.

There are numerous examples of variably labeled urea-based molecules with extremely high murine kidney uptake [18, 19, 23, 48, 49].

In a modified application of the chick chorioallantoic-membrane (CAM) grafting technique, we have transplanted 11-day-old undifferentiated embryonic murine kidney rudiments and studied their differentiation and early morphogenesis.

Our results indicate that the CAM is an efficient site for in vitro murine kidney development with both vascularization of the explant and extensive maturation, including the appearance of primitive nephron units.