The TMA slides were initially assessed by light microscope assessment of staining quality and specificity.
Immunostained sections were imaged with a digital Olympus microscope and assessment of levels of mGluR5 and arrestin immunoreactivity was performed utilizing the Image-Pro programograMedia CyberneticsicSilver Springing, MD).
Immunostained sections were imaged with a digital Olympus microscope and assessment of levels of mTor, Atg7, LC3 and Cathepsin D immunoreactivity was performed utilizing the Image-Pro Plus program (Media Cybernetics, Silver Spring, MD).
Optimization of a widefield structured illumination microscope for non-destructive assessment and quantification of nuclear features in tumor margins of a primary mouse model of sarcoma.
It did require cultured cells to be physically moved between tissue culture incubator and microscope for assessment, thus care had to be taken when handling weakly adherent cells.
Currently, pathologists analyze cells based mainly on their appearance under the microscope, and their assessment can vary widely.
The sections were imaged using a Zeiss LSM 510 META Confocal Microscope, and cell size and number assessments were made using the ImageJ software package.
Twelve plants were considered for the root mycorrhization intensity assessment and five microscope slides were analyzed per plant, each slide containing 20 root pieces of 1 cm.
After de-fatting the tissue in acetone, the mammary epithelia was stained with iron/hematoxylin and inspected under a microscope for assessment of overall development.
With the characteristisation study of pH, viscosity, transmission electron microscope (TEM) and stability assessment study the formulated nanoemulsion has the potential to penetrate blood brain barrier in the treatment of epilepsy.
