Examples of microscope

Example from the Hansard archive. Contains Parliamentary information licensed under the Open Parliament Licence v3.0
Other fungi and psoriasis can produce similar changes, but the diagnosis can be established by looking at nail clippings under a microscope.
The germinated and nongerminated seeds were counted using a binocular microscope.
With pieces of tape, pollen was sampled from forehead, throat and cheeks and studied in a scanning electron microscope.
The number of stomata was counted at each point, using a microscope with a lattice micrometer.
Fifty segments per seedling were examined using a light microscope under 400 x magnification.
The depth of focus within the tissue was determined from the micrometer on the focus mechanism of the microscope, which was recorded for each photograph.
Densities in each region were counted using a reticule placed in the optics of the microscope (110 mm 110 mm area).
The oocytes were then examined under a phase-contrast microscope.
Isolated follicles were measured with an eyepiece micrometer in a stereoscopic microscope.
The retinas were removed from the eyes, and after making several radial cuts at its edge, flat-mounted onto a microscope slide.
Fertilisation was determined under a phase-contrast microscope, recording pronuclear formation and 2-cell formation at 5 and 24 h after insemination, respectively.
They were easily distinguishable under the dissection microscope.
Exocytoses start as early as the first minute after fertilisation and can be observed continuously for more than 20 min on the microscope stage.
Sections were examined at the light microscope level, and those with substantial filling of isthmotectal or retinotectal axons were selected for processing for electron microscopy.
At 12 h intervals eggs were morphologically evaluated for 9 days at x 200 and x 400 with an inverted microscope.
The status of the acrosomes of bound spermatozoa was also examined under the high power of a phase-contrast microscope.
Ten to twelve hours after insemination, the number of pronuclei was counted under a dissection microscope to determine the ploidy of fertilised ova.
Next, a microcapillary was fixed to the instrument holder of the micromanipulator and the tip was focused under the microscope.
At the light microscope level no differences in testicular histology were observed in comparison with the controls.
Evaluations were performed in an inverted microscope at x400.
The confocal microscope scanned both fluorochromes simultaneously and multiple images from each rat retina were collected and subsequently analyzed.
The lenses were later replaced by microscopes, which enhanced their observations.
From
Wikipedia