Cell Phone Microscopy

Cell phone microscopy is the use of a smartphone camera, often paired with a compact optical attachment, to magnify and record specimens, making microscopy more portable and accessible for bioengineering research. In a typical system, lenses or other optical elements enlarge light from a sample and project the image onto the phone’s camera sensor, while software can support image capture, measurement, and analysis. These low-cost, portable platforms can support cell and tissue imaging, point-of-care diagnostics, environmental monitoring, and education, particularly where conventional microscopes are unavailable. Integration with computation and wireless communication also enables rapid data sharing and decentralized biological measurements.

Cell Phone Microscopy - Related Videos

Research

JoVE Journal - Bioengineering

Wide-field Fluorescent Microscopy and Fluorescent Imaging Flow Cytometry on a Cell-phone

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Cited by 32 •

2013

We review our recent results on the integration of fluorescent microscopy and imaging flow cytometry tools on a cell-phone using compact and cost-effective opto-fluidic attachments. These cell-phone based micro-analysis devices might be useful for cytometric analysis, such as performing various cell counting tasks as well as for high-throughput screening of e.g., water samples in resource limited settings.

Preparation of Drosophila S2 cells for Light Microscopy

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Cited by 24 •

2010

Drosophila Schneider (S2) cells are an increasingly popular system for the discovery and functional analysis of genes. Our goal is to describe some of the microscopic techniques that make S2 cells such an increasingly important experimental system.

In vivo Clonal Tracking of Hematopoietic Stem and Progenitor Cells Marked by Five Fluorescent Proteins using Confocal and Multiphoton Microscopy

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Cited by 11 •

2014

Combinatorial 5 fluorescent proteins marking of hematopoietic stem and progenitor cells allows in vivo clonal tracking via confocal and two-photon microscopy, providing insights into bone marrow hematopoietic architecture during regeneration. This method allows non-invasive fate mapping of spectrally-coded HSPCs-derived cells in intact tissues for extensive periods of time following transplantation.

Live Cell Imaging of F-actin Dynamics via Fluorescent Speckle Microscopy (FSM)

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Cited by 8 •

2009

Selection, microinjection, and imaging of fluorescently-labeled F-actin via fluorescent speckle microscopy (FSM).

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