Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Distribution Reliability and Automation01:25

Distribution Reliability and Automation

503
Distribution reliability in electrical power systems is critical for ensuring an uninterrupted power supply to consumers at minimal cost. According to IEEE Standard Terms, reliability is the probability that a device will function without failure over a specified time period or amount of usage. For electric power distribution, this translates to maintaining continuous power supply and addressing customer concerns over power outages. Several indices, as defined by IEEE Standard 1366-2012, are...
503
Immunofluorescence Microscopy01:12

Immunofluorescence Microscopy

13.4K
A fluorescence microscope uses fluorescent chromophores called fluorochromes, which can absorb energy from a light source and then emit this energy as visible light. Fluorochromes include naturally fluorescent substances (such as chlorophylls) and fluorescent stains that are added to the specimen to create contrast. Dyes such as Texas red and FITC are examples of fluorochromes. Other examples include the nucleic acid dyes 4’,6’-diamidino-2-phenylindole (DAPI), and acridine orange.
13.4K
Atomic Force Microscopy01:08

Atomic Force Microscopy

4.5K
Atomic force microscopy (AFM) is a type of scanning probe microscopy that can analyze topographic details of various specimens like ceramics, glass, polymers, and biological samples. AFM offers over 1000 times more resolution than the optical imaging system. Images generated from AFM are three-dimensional surface profiles, offering an advantage over the flat, two-dimensional images from other imaging techniques.
The AFM Probe
The probe is regarded as the heart of any AFM setup and comprises the...
4.5K
Overview of Microscopy Techniques01:22

Overview of Microscopy Techniques

16.2K
The early pioneers of microscopy opened a window into the invisible world of microorganisms. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes that leveraged nonvisible light, such as fluorescence microscopy that uses an ultraviolet light source and electron microscopy that uses short-wavelength electron beams. These advances significantly improved magnification, image resolution, and contrast. By comparison, the...
16.2K
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

1.3K
Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...
1.3K
Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

800
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...
800

You might also read

Related Articles

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

Sort by
Same author

Emergent Intercellular Junction Stability during Cyclic Tissue Loading.

Biophysical journal·2026
Same author

Boundary constraints can determine pattern emergence.

Development (Cambridge, England)·2026
Same author

Spatiotemporal mapping of the contractile and adhesive forces sculpting early C. elegans embryos.

Developmental cell·2026
Same author

3D epithelial cell topology tunes signaling range to promote precise patterning.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

The cytoplasm of living cells can sustain transient and steady intracellular pressure gradients.

eLife·2026
Same author

Deciphering the Nanoscale Architecture of Presynaptic Actin Using a Micropatterned Presynapse-on-Glass Model.

The Journal of neuroscience : the official journal of the Society for Neuroscience·2026
Same journal

PCSK5 promotes angiogenesis and cardiac repair after myocardial infarction.

Nature communications·2026
Same journal

PfApiAT2 is a proline transporter essential for the transmission of Plasmodium falciparum by the mosquito vector.

Nature communications·2026
Same journal

Transient distortions of the South Atlantic Anomaly radiation environments driven by electric fields.

Nature communications·2026
Same journal

Structural basis of the regulation by CDK11 kinase of early spliceosome activation and evidence for its proofreading by DHX15 helicase.

Nature communications·2026
Same journal

Structural and mechanistic insights into primer synthesis initiation by DNA primase.

Nature communications·2026
Same journal

Changes in heritability and shared environmentality of educational attainment across twentieth-century Norway.

Nature communications·2026
See all related articles

Related Experiment Video

Updated: Jan 27, 2026

Automated Multimodal Stimulation and Simultaneous Neuronal Recording from Multiple Small Organisms
08:28

Automated Multimodal Stimulation and Simultaneous Neuronal Recording from Multiple Small Organisms

Published on: March 3, 2023

1.6K

Automating multimodal microscopy with NanoJ-Fluidics.

Pedro Almada1,2, Pedro M Pereira1,2,3, Siân Culley1,2,3

  • 1MRC-Laboratory for Molecular Cell Biology, University College London, London, WC1E 6BT, UK.

Nature Communications
|March 16, 2019
PubMed
Summary
This summary is machine-generated.

We developed NanoJ-Fluidics, an automated, open-source system using low-cost hardware and software for complex microscopy workflows. This approach simplifies multimodal imaging for reproducible, high-content cellular studies.

More Related Videos

Combining Fluidic Devices with Microscopy and Flow Cytometry to Study Microbial Transport in Porous Media Across Spatial Scales
12:32

Combining Fluidic Devices with Microscopy and Flow Cytometry to Study Microbial Transport in Porous Media Across Spatial Scales

Published on: November 25, 2020

7.0K
Multimodal Hierarchical Imaging of Serial Sections for Finding Specific Cellular Targets within Large Volumes
11:19

Multimodal Hierarchical Imaging of Serial Sections for Finding Specific Cellular Targets within Large Volumes

Published on: March 20, 2018

10.9K

Related Experiment Videos

Last Updated: Jan 27, 2026

Automated Multimodal Stimulation and Simultaneous Neuronal Recording from Multiple Small Organisms
08:28

Automated Multimodal Stimulation and Simultaneous Neuronal Recording from Multiple Small Organisms

Published on: March 3, 2023

1.6K
Combining Fluidic Devices with Microscopy and Flow Cytometry to Study Microbial Transport in Porous Media Across Spatial Scales
12:32

Combining Fluidic Devices with Microscopy and Flow Cytometry to Study Microbial Transport in Porous Media Across Spatial Scales

Published on: November 25, 2020

7.0K
Multimodal Hierarchical Imaging of Serial Sections for Finding Specific Cellular Targets within Large Volumes
11:19

Multimodal Hierarchical Imaging of Serial Sections for Finding Specific Cellular Targets within Large Volumes

Published on: March 20, 2018

10.9K

Area of Science:

  • Cellular biology
  • Microscopy techniques
  • Biotechnology

Background:

  • Advanced microscopy is essential for understanding cellular events.
  • Current workflows for combining and multiplexing microscopy are often complex and elaborate.
  • Need for accessible, reproducible, and automated solutions in high-content imaging.

Purpose of the Study:

  • To present a robust, open-source approach for automated, sequential treatment, labeling, and imaging of cells.
  • To simplify the implementation of high-content, multimodal imaging on various microscopes.
  • To demonstrate the system's capability in advanced microscopy applications.

Main Methods:

  • Development of NanoJ-Fluidics, an integrated system using affordable Lego hardware and ImageJ-based software.
  • Automation of cell treatment, labeling, and imaging sequences.
  • Application of the system to live-to-fixed and multiplexed super-resolution microscopy.

Main Results:

  • NanoJ-Fluidics enables reproducible, high-content, multimodal imaging with ease of implementation.
  • Demonstrated successful application in event-driven, super-resolved live-to-fixed experiments.
  • Validated multiplexed STORM/DNA-PAINT experiments using the automated system.

Conclusions:

  • NanoJ-Fluidics offers a cost-effective and reproducible solution for complex microscopy workflows.
  • The system enhances accessibility to advanced imaging techniques for cellular studies.
  • Facilitates high-content, multimodal imaging, advancing cellular event analysis.