Microscopic Dissection

Microscopic dissection is a precision technique for separating and examining small biological structures under magnification, allowing researchers to study tissues, organs, embryos, or individual anatomical features that cannot be resolved by unaided vision. Using a stereomicroscope or similar instrument, the operator stabilizes the specimen and manipulates fine needles, forceps, or blades to isolate structures while preserving their spatial relationships and minimizing damage. In biology, microscopic dissection supports developmental studies, comparative anatomy, histological preparation, and targeted tissue collection for molecular analysis. The technique links visible anatomy with cellular and molecular investigations, providing detailed evidence about structure, organization, and function.

Microscopic Dissection - Related Videos

Research

JoVE Journal - Developmental Biology
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Analysis of Zebrafish Kidney Development with Time-lapse Imaging Using a Dissecting Microscope Equipped for Optical Sectioning

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Cited by 2 •

2016

The method described here allows time-lapse analysis of organ development in zebrafish embryos by using a fluorescence dissecting microscope capable of performing optical sectioning and simple strategies of readjustment to correct focal and planar drift.

Research

JoVE EoE - Urinary Tract Cancer

Kidney Flat Mount Preparation: A Procedure to Dissect and Prepare a Flat Mount for Microscopic Analysis of Adult Zebrafish Kidney

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2023

This video demonstrates the dissection and preparation of a flat mount of the adult zebrafish kidney. The prepared flat mount can be visualized under the microscope for specimen analysis.

Research

JoVE Journal - Biology
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Dissection of Organs from the Adult Zebrafish

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Cited by 167 •

2010

This protocol describes a procedure for identifying and dissecting organs from the adult zebrafish.

Dissection of Saccharomyces Cerevisiae Asci

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Cited by 8 •

2009

Micromanipulation of yeast cells is needed for meiotic genetic analysis or to select diploid zygotes. These micromanipulations are carried out using the microneedle of a dissection microscope. The microneedle is used to relocate cells and is controlled by a micromanipulator which are available with various degrees of automation.

Immunostaining of Dissected Zebrafish Embryonic Heart

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Cited by 35 •

2012

A rapid way to conduct immunostaining of zebrafish embryonic heart is described. Compared to the whole mount immunostaining approach, this method dramatically increases the penetration of the antibodies, which allows obtaining high resolution images that reveal cellular/subcellular structures in the heart within a much reduced processing time.

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