Dissecting Microscope Observation

Dissecting microscope observation is the examination of whole, relatively large specimens with a stereomicroscope, allowing their external structures and spatial relationships to be viewed without sectioning. The instrument uses separate optical paths for each eye to produce a three-dimensional image, typically at low magnification with reflected or transmitted illumination, while maintaining enough working distance for handling the specimen. In biology, this approach supports the study of plants, insects, embryos, tissues, and small organisms, including their morphology, movement, and developmental features. It is also valuable for sorting samples, performing microdissections, and guiding precise manipulation during research and teaching.

Dissecting Microscope Observation - Related Videos

Research

JoVE Journal - Bioengineering

Continuous High-resolution Microscopic Observation of Replicative Aging in Budding Yeast

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Cited by 10 •

2013

We describe here the operation of a microfluidic device that allows continuous and high-resolution microscopic imaging of single budding yeast cells during their complete replicative and/or chronological lifespan.

Heart Dissection: A Method to Observe Zebrafish Cardiac Development

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2023

This video describes a technique of isolating the heart from a zebrafish at multiple developmental stages to study cardiac development, maturation, and ageing.

Drosophila Larva Imaginal Disc Dissection: A Method to Observe Developing Epithelia

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2023

When staining Drosophila imaginal discs, often a rough dissection is performed where the discs are exposed but remain attached to the body. Once stained, the discs of interest are isolated and mounted. The example protocol demonstrates a procedure for wing imaginal disc dissection and mounting.

Microscopic Observation of Lymphocyte Dynamics in Rat Peyer's Patches

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Cited by 3 •

2020

Here, we describe a precise method for collecting thoracic duct lymphocytes and observing the migration of gut-tropic lymphocytes in rat Peyer’s patches for 3 hours using time-lapse photography. This technique can clarify how the dynamics of lymphocytes are affected under inflammatory conditions.

Multiphoton Microscopic Observation of Vessels in Mouse Liver Tissue

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2021

In this experiment, a mouse is injected in its tail vein with Rhodamine B isothiocyanate–dextran that can stain blood vessels. After the liver is exposed and fixed, a specific part of the liver can be selected to observe the deep tissue in the living body using multiphoton microscopy.

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