Microdissection Procedure

Microdissection is a procedure that isolates small, defined regions of tissue or individual cells from a larger biological specimen for focused analysis. Using a microscope and specialized tools, researchers identify the target area and separate it mechanically or with laser-guided cutting while preserving its anatomical context and molecular material. The recovered samples can support DNA, RNA, protein, or histological studies, linking cellular composition to tissue structure and function. In biology, microdissection helps investigate heterogeneous tissues, compare normal and diseased regions, and obtain cell populations for applications such as gene-expression profiling, pathology, developmental research, and disease mechanism studies.

Microdissection Procedure - Related Videos

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JoVE EoE - Cancers of the Nervous System

Cryopreserved Tissue Section Fixation and Staining: A Procedure to Process Frozen Brain Tissue Sections for Laser Microdissection

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2023

This video presents the fixation and staining method to process frozen mouse brain tumor tissue. The processed tissue helps differentiate and obtain a specific population of cells during subsequent laser capture microdissection.

Laser Capture Microdissection of Drosophila Peripheral Neurons

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Cited by 25 •

2010

In this video-article we present a method for isolating single or multiple Drosophila da neurons from third instar larvae using the infrared capture (IR) class of Laser Capture Microdissection (LCM). RNA obtained from the isolated neurons can be readily used for downstream applications including qRT-PCR or microarray analyses.

Laser Capture Microdissection of Mammalian Tissue

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Cited by 25 •

2007

Laser capture microscopy, also known as laser microdissection (LMD), enables the user to isolate small numbers of cells or tissues from frozen or ...

Microdissection of Zebrafish Embryonic Eye Tissues

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Cited by 15 •

2010

This article describes an approach to microdissect zebrafish retinas with and without retinal pigment epithelium attached, from one to three days postfertilization embryos.

Laser Capture Microdissection of Neurons from Differentiated Human Neuroprogenitor Cells in Culture

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Cited by 3 •

2013

Human neuroprogenitor cells (NPCs) were expanded under proliferating conditions. NPCs were differentiated into neuron-rich cultures in the presence of a combination of neurotrophins. Neuronal markers were detected by immunofluorescence staining. To isolate a pure population of neurons, NPCs were differentiated on PEN membrane slides and laser capture microdissection was performed.

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