Exact(8)
Photomicrograph from a tissue cross section obtained after RP.
Fusion of the transverse T2w MRI image with the corresponding tissue cross section (D).
A TEM image of a tissue cross section is shown in Fig. 3c.
The type, amount, and distribution of induced positron-emitting radionuclides depend on the irradiated tissue cross section, the photon spectrum, and the possible perfusion-driven washout.
Cells were grown on the MLC insert in Dulbecco′s Modified Eagle′s Medium (LifeTechnologies Inc. Burlington, ON) with 10 % Fetal Bovine Serum (Sigma-Aldrich, Oakville, ON). Figure 3d shows an image of an unstained tissue cross section of MCF-7 cells.
Each OCT image corresponded to a two-dimensional tissue cross section 5 mm wide by 2.6 mm deep.
Similar(52)
d, e Unstained and stained images of MCL tissue cross sections, respectively.
IF analysis of tissue cross sections involves fixation of tissues with a 10% formalin solution followed by paraffin embedding, dehydration with ethanol, sectioning, and staining of the tissues once they have been deposited on slides.
For TUNEL-P2X7 co-staining, tissue cross sections were first assayed for TUNEL, followed by P2X7 immunostaining.
Tissue cross sections (8 μm thick) were cut on a rotary microtome (AO Spencer 820 Microtome; American Optical) using Leica blades.
Whole UC tissue cross sections were embedded in OCT mounting media (#361603E, VWR, Leicestershire, UK), snap frozen in liquid nitrogen and stored at -80°C.
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