Sentence examples for a selection of tissue from inspiring English sources

Before processing for electron microscopical analysis, MLN sections from control and terminally-scrapie-affected mice were first prepared from a selection of tissue blocks for light microscopy and immunolabelled to detect PrPd, IgG, IgM and ubiquitin.

To complement this approach we included a selection of tissues from shoot and root in order to evaluate Rhizobium-legume interactions and shoot-root communication, which is known to be essential for controlling nodule number [33].

In a selection of tissues, macrophage identity was confirmed by double staining for PLXND1 and CD68.

In order to analyse the expression of all the genes in Table 2, a selection of tissues were collected across different developmental stages/tissues and under different stress conditions in wild type rice, cv.

A selection of tissues, including spleen, kidney, liver, epigonal and Leydig organs, pancreas, gill, skin, brain, heart and muscle and whole blood, were collected from three outwardly healthy dogfish.

To our knowledge, this is the first transcriptomic study to show differentially expressed genes in a selection of tissues in the MRL/MpJ mouse by comparative analysis with two reference strains.

We examined Plexin D1 expression in clinical solid tumors (n = 77) of different origin, a selection of pre-malignant lesions (n = 29) and a variety of non-tumor related tissues (n = 52) by immunohistochemistry. Signals were verified in a selection of tissues via mRNA in situ hybridization.

Various levels of GFP staining were seen in all the organs and tissues collected from fetal and neonatal vector-recipient mice when viewed under a light microscope, and representative images were acquired (Fig. 2 A ). Higher power images were also captured from a selection of tissues from the mice that received vector at the 2 different stages of development (Fig. 2 A, insets; ssAAV9 injection).

Herein we present a detailed investigation of the relation between gene expression and the disease-associated allele at rs2891168 and other associated genotypes in a selection of relevant tissues.

Identity of macrophages was confirmed by double staining a selection of analyzed tissues for PLXND1 and CD68 (not shown).

In a further set of experiments, we then assayed Ins P6 levels in a selection of rat tissues, and the results are shown in Table 1.