Hanging Drop Method

The Hanging Drop Method is a microscopy technique that places a liquid specimen in a suspended drop beneath a coverslip, allowing microorganisms to be observed without immediate drying or compression. A small drop is mounted on a coverslip and sealed over a concave slide, creating a stable chamber in which cells can remain suspended and move freely; directional movement can be distinguished from Brownian motion. In biology, the method is especially useful for assessing bacterial motility, observing cell behavior, and examining living microorganisms over time. It provides a simple, low-cost alternative to fixed preparations when studying characteristics that depend on viable, actively moving cells.

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Hanging Drop Method: A Technique to Generate 3D Melanoma Spheroids

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2023

This video describes the technique of generating three-dimensional spheroids via the hanging drop method using melanoma cells. The generated in vitro three-dimensional (3D) organotypic melanoma spheroid model can portray the in vivo architecture of malignant melanoma and may give insights into intra-tumoral...

In vitro Differentiation of Mouse Embryonic Stem (mES) Cells Using the Hanging Drop Method

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Cited by 96 •

2008

This video demonstrates how to conduct in vitro differentiation of mouse embryonic stem cells to embryoid bodies using the hanging drop method.

Developing Neuron Balls Using a Hanging Drop Culture Technique

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2025

This video demonstrates the process of generating neuron balls using a hanging drop culture technique. Within the hanging drops, cells move towards the bottom, self-assembled into three-dimensional structures forming neuron balls, which can be used for neurobiological studies.

Generating Neural Progenitors from Mouse Embryonic Stem Cells by the Hanging Drop Method

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2025

The video demonstrates the differentiation of mouse embryonic stem cells (mESCs) to embryoid bodies (EBs) by the hanging drop method. Upon suspending the mESCs in hanging drops and incubating, the cells aggregate to form EBs, which are further differentiated into neuronal progenitor cells (NPCs) using a differentiation medium supplemented with retinoic acid (RA).

The Preparation of Drosophila Embryos for Live-Imaging Using the Hanging Drop Protocol

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Cited by 34 •

2009

A simple, inexpensive, and effective method of preparing Drosophila embryos for live-imaging analysis is presented. Our protocol provides humidity and gas exchange and does not compress the Drosophila embryo. This method is suitable for GFP-based live imaging of Drosophila embryos using a stereomicroscope or upright compound microscope.

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