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Prostates from transgenic mice were dissected using a dissection microscope, fixed in 10% buffered formalin and embedded in paraffin.
Sporulation cultures were digested with Zymolyase 20T in sorbitol buffer and tetrads were dissected on YPD plates using a dissection microscope; 10 cells of freshly dissected spores were allowed to grow for 24 hr in YPD media at 30°.
Brains were placed in cold Hybernate E/A medium (BrainBits, Springfield, IL), and cortices containing the hippocampus were dissected out using a dissection microscope.
The nature of stigma, style and the position of ovaries were identified by using a dissection microscope.
Each filter paper was spread on petri dish and spores were counted using a dissection microscope at 40 × magnification.
Dissection was done using a dissection microscope (×3.5), delineating meticulously the arcuate artery, dorsal metatarsal arteries and the small branches arising from the metatarsal arteries.
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We used a dissection microscope to classify arthropods to order.
Worm dissections were performed using a dissecting microscope on either live or frozen adult D. immitis by mounting them on a wax pad and making a long head-to-tail incision using iridectomy scissors.
After drying the number of spots was scored by use of a dissection microscope.
The fibrous capsule that surrounds each parasite was carefully separated with the use of a dissection microscope.
The brain was dissected by a trained neurophysiologist using a binocular dissection microscope on an ice-chilled surface.
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