Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Related Concept Videos

Three-Dimensional Microscopy in Microbiology

Three-Dimensional Microscopy in Microbiology

Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...

Confocal Fluorescence Microscopy

Confocal Fluorescence Microscopy

Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by

Same author

Extracellular vesicles from wild-type Epstein-Barr virus-transformed B-cells export host DNA and EBV EBER1.

bioRxiv : the preprint server for biology·2026

Same author

Extracellular Vesicles from Glioblastoma Cells Reflect 2D vs. 3D Culture Adaptation and Resistance to Temozolomide.

Molecular & cellular proteomics : MCP·2026

Same author

Analysis of plasma extracellular vesicles in normal-weight and overweight type 2 diabetes mellitus using multimodal SERS and RNA-Seq.

Diabetes research and clinical practice·2026

Same author

<i>Isoquercetin treatment of mouse sickled red blood cells shows a</i> discernible deformability and sickling phenotype.

bioRxiv : the preprint server for biology·2026

Same author

Selective capture and digital counting of intact HIV pseudovirus using designer DNA nets, tethered motion, and photonic resonator interferometric scattering microscopy.

APL bioengineering·2026

Same author

Analysis of Plasma Extracellular Vesicles in Normal-Weight and Overweight Type 2 Diabetes Mellitus Using Multimodal SERS and RNA-Seq.

bioRxiv : the preprint server for biology·2026

Same journal

Design Principles for Fluid Molecular Ferroelectrics.

Advanced materials (Deerfield Beach, Fla.)·2026

Same journal

Generating Unconventional Spin-Orbit Torques With Patterned Phase Gradients in Tungsten Thin Films.

Advanced materials (Deerfield Beach, Fla.)·2026

Same journal

An In Situ H<sub>2</sub>S-Activated Plasmonic Nanozyme for Near-Infrared II Photo-Thermoelectric Catalytic Therapy.

Advanced materials (Deerfield Beach, Fla.)·2026

Same journal

A Recyclable and Sustainable Hydroxypropyl Methylcellulose Electrolyte for Electrochromic Devices.

Advanced materials (Deerfield Beach, Fla.)·2026

Same journal

Perovskite Heterostructures for Optoelectronic Applications.

Advanced materials (Deerfield Beach, Fla.)·2026

Same journal

Light-Written Nonvolatile Polarization via Defect-Engineered Charge Trapping.

Advanced materials (Deerfield Beach, Fla.)·2026

See all related articles

Search research articles

Related Experiment Video

Updated: Apr 11, 2026

Microfluidic Imaging Flow Cytometry by Asymmetric-detection Time-stretch Optical Microscopy ATOM

Microfluidic Imaging Flow Cytometry by Asymmetric-detection Time-stretch Optical Microscopy ATOM

Published on: June 28, 2017

Levitational Image Cytometry with Temporal Resolution.

Savas Tasoglu^1,2, Joseph A Khoory³, Huseyin C Tekin^1,2

¹Department of Radiology, Stanford School of Medicine, Demirci Bio-acoustic MEMS in Medicine (BAMM) Labs, Canary Center at Stanford for Cancer Early Detection, Palo Alto, CA, 94304, USA.

Advanced Materials (Deerfield Beach, Fla.)

|June 11, 2015

Summary

This summary is machine-generated.

A novel magnetic levitation device enables real-time, label-free separation and monitoring of cells. This technology analyzes cellular changes based on magnetic and density properties for biological studies.

Keywords:

biological materials cell screening cell separation cells magnetic levitation

More Related Videos

Cortical Actin Flow in T Cells Quantified by Spatio-temporal Image Correlation Spectroscopy of Structured Illumination Microscopy Data

Cortical Actin Flow in T Cells Quantified by Spatio-temporal Image Correlation Spectroscopy of Structured Illumination Microscopy Data

Published on: December 17, 2015

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

Published on: January 30, 2020

Related Experiment Videos

Last Updated: Apr 11, 2026

Microfluidic Imaging Flow Cytometry by Asymmetric-detection Time-stretch Optical Microscopy ATOM

Microfluidic Imaging Flow Cytometry by Asymmetric-detection Time-stretch Optical Microscopy ATOM

Published on: June 28, 2017

Cortical Actin Flow in T Cells Quantified by Spatio-temporal Image Correlation Spectroscopy of Structured Illumination Microscopy Data

Cortical Actin Flow in T Cells Quantified by Spatio-temporal Image Correlation Spectroscopy of Structured Illumination Microscopy Data

Published on: December 17, 2015

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

Published on: January 30, 2020

Area of Science:

Biophysics
Cell Biology
Biotechnology

Background:

Cell separation and monitoring are crucial for biological research.
Existing methods often require labels or lack real-time analysis capabilities.
Understanding cellular changes requires precise measurement of their physical properties.

Purpose of the Study:

To develop a novel magnetic levitation device for cell analysis.
To enable real-time, label-free separation and monitoring of cell populations.
To investigate cellular processes by tracking changes in magnetic and density signatures.

Main Methods:

Utilized magnetic levitation principles for device construction.
Developed a system for label-free, real-time cell population analysis.
Measured cell populations based on their intrinsic magnetic and density characteristics.

Main Results:

Demonstrated a simple yet powerful magnetic levitation device.
Achieved real-time, label-free separation and high-resolution monitoring of cells.
Showcased the ability to study cellular processes via changes in magnetic and density signatures.

Conclusions:

The magnetic levitation device offers a versatile tool for cell analysis.
This label-free, real-time method facilitates the study of dynamic cellular changes.
The technology has broad applications in understanding cell biology and material science.