Electron Multiplying Camera

An electron multiplying camera is a highly sensitive digital imaging device that detects and amplifies weak light signals, making it valuable when biological samples produce only a few photons. It uses a charge-coupled device to convert incoming photons into electrons, then passes those electrons through a multiplication register where repeated impact ionization creates additional charge before readout, reducing the effect of electronic noise. In biology, electron multiplying cameras support low-light fluorescence imaging, live-cell microscopy, and measurements of rapid or faint cellular events. Their sensitivity can improve image quality while enabling shorter exposures and reduced illumination of light-sensitive specimens.

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Research

JoVE Journal - Bioengineering

Microfluidic Platform with Multiplexed Electronic Detection for Spatial Tracking of Particles

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Cited by 8 •

2017

We demonstrate a microfluidic platform with an integrated surface electrode network that combines resistive pulse sensing (RPS) with code division multiple access (CDMA), to multiplex detection and sizing of particles in multiple microfluidic channels.

Research

JoVE Journal - Biochemistry

RGBradford: Protein Quantitation with a Smartphone Camera

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Cited by 1 •

2023

This paper provides a protocol for protein quantification using the Bradford assay and a smartphone as an analytical device. Protein levels in samples can be quantified using color data extracted from a picture of a microplate taken with a smartphone.

Correlative Light- and Electron Microscopy Using Quantum Dot Nanoparticles

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Cited by 12 •

2016

A method is described whereby quantum dot (QD) nanoparticles can be used for correlative immunocytochemical studies of epoxy embedded human pathology tissue. We employ commercial antibody fragment conjugated QDs that are visualized by widefield fluorescence light microscopy and transmission electron microscopy.

Research

JoVE Journal - Biochemistry
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Micropatterning Transmission Electron Microscopy Grids to Direct Cell Positioning within Whole-Cell Cryo-Electron Tomography Workflows

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Cited by 29 •

2021

The goal of this protocol is to direct cell adhesion and growth to targeted areas of grids for cryo-electron microscopy. This is achieved by applying an anti-fouling layer that is ablated in user-specified patterns followed by deposition of extra-cellular matrix proteins in the patterned areas prior to cell seeding.

Multiplex Cyclic Fluorescent Immunohistochemistry

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Cited by 1 •

2024

Multiplex cyclic immunohistochemistry allows in situ detection of multiple markers simultaneously using repeated antigen-antibody incubation, image scanning, and image alignment and integration. Here, we present the operating protocol for identifying immune cell substrates with this technology in lung cancer and paired brain metastasis samples.

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