Microdissection Scissors

Microdissection scissors are precision instruments used to cut, separate, and manipulate small biological specimens during laboratory procedures. Their fine, sharp blades and compact design enable controlled dissection under magnification, allowing researchers to isolate tissues, organs, vessels, or other microscopic structures while minimizing surrounding damage. In biology, these scissors support anatomical studies, tissue sampling, embryo and model-organism dissection, and preparation of specimens for microscopy, molecular analysis, or cell culture. Their performance depends on blade sharpness, tip geometry, and careful handling, making them valuable for reproducible sample preparation and precise experimental work.

Microdissection Scissors - Related Videos

Research

JoVE Journal - Neuroscience

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 ...

Multilevel Microdissection and Functional-Structural Profiling of Human Renal Arterial Branches

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2025

This article presents a step-by-step protocol for the isolation and functional evaluation of human renal arterial branches, facilitating preclinical studies for pharmaceutical development.

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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