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Area per high-power field for some microscope types: Olympus BX50, BX40 or BH2 or AO: 0.096 mm 2 [1] AO with 10x eyepiece: 0.12 mm 2 [1] Olympus with 10x eyepiece: 0.16 mm 2 [1] Nikon Eclipse E400 with 10x eyepiece and 40x objective: 0.25mm 2 [2] Leitz Ortholux: 0.27 mm 2 [1] Leitz Diaplan: 0.31 mm 2 [1]
Date/Time Thumbnail Dimensions User Comment; current: 12:22, 6 April 2014: 3 min 52 s, 480 × 360 (7.38 MB): Jacopo Werther == {{int:filedesc}} == {{Information |Description = Step-by-step video and audio instructions on how to prepare a wet mount specimen of eukaryotic animal cells; specifically Human epithelial cells from the inside of the cheek.
The proportion of the cells counted applies if not all inner squares within a set square are counted (i.e., if only 4 out of the 20 in a corner square are counted, then this term will equal 0.2). When counting large squares with a volume of 100 nanoliter (nL), a multiplication by 10000 leads to the desired cell count per milliliter.
The shape and texture in each individual grain is made visible through the microscope. [7] As the microscopic scale covers any object that cannot be seen by the naked eye, yet is visible under a microscope, the range of objects that fall under this scale can be as small as an atom, visible underneath a transmission electron microscope. [8]
Stratified cuboidal epithelium, highlighting the nucleuses, the rest of the epithelial cells, and underlying connective tissue. Stratified cuboidal epithelium is a type of epithelial tissue composed of multiple layers of cube-shaped cells. Only the most superficial layer is made up of cuboidal cells, and the other layers can be cells of other ...
The dimensionless quantities often represent the degree of deviation from an ideal shape, such as a circle, sphere or equilateral polyhedron. [1] Shape factors are often normalized, that is, the value ranges from zero to one. A shape factor equal to one usually represents an ideal case or maximum symmetry, such as a circle, sphere, square or cube.
A drop of cell culture is placed in the space between the chamber and the glass cover, filling it via capillary action. [1] Looking at the sample under the microscope, the researcher uses the grid to manually count the number of cells in a certain area of known size. The separating distance between the chamber and the cover is predefined, thus ...
Live-cell imaging is the study of living cells using time-lapse microscopy. It is used by scientists to obtain a better understanding of biological function through the study of cellular dynamics. [1] Live-cell imaging was pioneered in the first decade of the 21st century.