Sentences with phrase «eosin stained»

This hematoxylin and eosin stained slide of a surgically removed (resected) primary pancreatic tumor shows a cluster of immune cells (lymphoid aggregate) observed next to a pancreatic tumor lesion in a patient treated with a GM - CSF vaccine 2 weeks before surgical removal of the primary tumor.

For morphometric analysis, the gastrocnemius and plantaris muscles were sectioned serially to their widest point using a cryostat, and fiber diameters were measured (as the shortest distance across the fiber passing through the midpoint) from hematoxylin and eosin stained sections.

Haematoxylin and eosin staining was performed according to standard procedures.

Testes were fixed in Bouins» solution overnight and sectioned at 5 - µm thickness for hematoxylin / eosin staining.

J, Hematoxylin and eosin staining of teratoma sections generated from integration - free iPSC lines showing differentiation in three germ layers: goblet cells in gastro - intestinal (GI) tract (endoderm); neural rosettes (ectoderm) and blood vessels, muscle and cartilage / bone (mesoderm).

B, Hematoxylin and eosin stains of the solid - tumor biopsy pre - and post-talazoparib were consistent with approximately 60 % tumor purity.

Not exact matches

Pathologists typically use hematoxylin and eosin (H&E) staining to highlight the intestinal structure.

Finally, they stained the layers with two compounds: hematoxylin, which brings DNA into relief, and eosin, which highlights details inside cells.

Furthermore, we analyzed sections from tissues directly associated with glucose homeostasis (liver and skeletal muscle), stained with hematoxylin and eosin, over a range of 250 µm.

3 - µm sections were stained with hematoxylin and eosin (HE) and examined by light microscopy.

Multiple hematoxylin - eosin - stained sections showed the presence of endothelium with intact Descemet membrane and no stromal tissue.

Fetal thoraces and adult hearts and aortas were embedded in paraffin, exhaustively sectioned (10 µm, Leica RM 2235 microtome, Germany) and processed for haematoxylin and eosin (H&E) staining.

Sections from all cases were subjected to stain with haematoxylin and eosin (H&E) for histopathological examination and immunohistochemical technique for Cyclin D1 in addition using flow cytometric technique to perform cell cycle analysis.

Lung sections were separately stained with hematoxylin and eosin (H&E) and an immunohistochemical protocol using an eosinophil - specific staining procedure with a monoclonal antibody to a major basic protein of eosinophils.

The infected cells ruptured, and eosinophilic particles were found with hematoxylin and eosin (HE) staining (Fig. 4A and B).

Histological sections were stained with hematoxylin - eosin.

Sections were processed with hematoxylin and eosin (HE) staining.

(A — C) Sections of testes of 3 - year - old (A) and 5 - year - old monkeys (B, C) were stained with hematoxylin and eosin.

Paraffin - embedded tissue sections were cut into 5 - μm thickness, fixed and stained with haematoxylin and eosin (H&E).

For the histological analysis, the samples were sectioned into 5 - µm thickness and stained with hematoxylin and eosin.

Paraffin sections were fixed according to standard procedure and stained with hematoxylin and eosin.

Sections (5 - μm thick) across the seminiferous tubules were deparaffinized, hydrated, and stained with hematoxylin and eosin for histological examination.

Every 50th section was stained with hematoxylin and eosin for nuclear boundaries and counterstained with Luxol fast blue for myelin boundaries.

The tissues were then paraffin embedded, sectioned, stained with hematoxylin and eosin, and examined for the presence of tissue representatives of all three germ layers.

Twenty - two sections of paraffin - embedded tissue were stained for Luxol fast blue, hematoxylin and eosin, Bielschowsky silver, phosphorylated tau (ptau)(AT8), α - synuclein, amyloid - β, and phosphorylated transactive response DNA binding protein 43 kDa (pTDP - 43) using methods described previously.16 In some cases, large coronal slabs of the cerebral hemispheres were also cut at 50 μm on a sledge microtome and stained as free - floating sections using AT8 or CP - 13.16,17

The microscopic description is usually something like this: hemotoxylin and eosin - stained sections of the mass and adjacent tissue contained irregular lobules of fine mineralized material cuffed by macrophages and multinucleated giant cells....

Light microscopic evaluation of histological and histochemical stains and reactions was performed according to standard protocols [20] and included hematoxylin and eosin, modified Gomori trichrome, periodic acid Schiff, phosphorylase, esterase, myofibrillar ATPase reaction at preincubation pH of 9.8, 4.5, and 4.3, reduced nicotinamide adenine dinucleotide - tetrazolium reductase, succinic dehydrogenase, acid phosphatase, and oil red O.

Most of the eyes were fixed in formalin, and routinely processed for paraffin embedding and hematoxylin and eosin (H&E) staining.