File:From-Dynamic-Live-Cell-Imaging-to-3D-Ultrastructure-Novel-Integrated-Methods-for-High-Pressure-pone.0009014.s012.ogv
From Wikimedia Commons, the free media repository
Jump to navigation
Jump to search
No higher resolution available.
From-Dynamic-Live-Cell-Imaging-to-3D-Ultrastructure-Novel-Integrated-Methods-for-High-Pressure-pone.0009014.s012.ogv (Ogg Theora video file, length 28 s, 758 × 462 pixels, 1.58 Mbps, file size: 5.33 MB)
File information
Structured data
Captions
Summary
[edit]DescriptionFrom-Dynamic-Live-Cell-Imaging-to-3D-Ultrastructure-Novel-Integrated-Methods-for-High-Pressure-pone.0009014.s012.ogv |
English: Model of the GFP-BIN1 fluorescent signal. The fluorescent signal has been thresholded to modelize the GFP-BIN1 tubules induced by overexpression in COS-1 cells. Rotation of the model, superimposed with the fluorescent signal, shows the organization of the tubular network inside the cell. Snapshots of this movie are shown in figure 5 for correlation with immuno-EM. |
||
Date | |||
Source | Video S6 from Spiegelhalter C, Tosch V, Hentsch D, Koch M, Kessler P, Schwab Y, Laporte J (2010). "From Dynamic Live Cell Imaging to 3D Ultrastructure: Novel Integrated Methods for High Pressure Freezing and Correlative Light-Electron Microscopy". PLOS ONE. DOI:10.1371/journal.pone.0009014. PMID 20140253. PMC: 2815783. | ||
Author | Spiegelhalter C, Tosch V, Hentsch D, Koch M, Kessler P, Schwab Y, Laporte J | ||
Permission (Reusing this file) |
|
||
Provenance InfoField |
|
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 09:28, 31 October 2012 | 28 s, 758 × 462 (5.33 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
You cannot overwrite this file.
File usage on Commons
There are no pages that use this file.
Transcode status
Update transcode statusMetadata
This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file. The timestamp is only as accurate as the clock in the camera, and it may be completely wrong.
Author | Spiegelhalter C, Tosch V, Hentsch D, Koch M, Kessler P, Schwab Y, Laporte J |
---|---|
Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Model of the GFP-BIN1 fluorescent signal. The fluorescent signal has been thresholded to modelize the GFP-BIN1 tubules induced by overexpression in COS-1 cells. Rotation of the model, superimposed with the fluorescent signal, shows the organization of the tubular network inside the cell. Snapshots of this movie are shown in figure 5 for correlation with immuno-EM. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2010 |
Categories:
- Videos of research methods
- COS cells
- Electron microscope tomography
- Videos of green fluorescent proteins
- Luminescent proteins
- Confocal microscopic movies from Open Access Journals
- Scanning electron microscopy
- Molecular dynamics simulation
- Non-receptor protein tyrosine phosphatases
- Recombinant fusion proteins
- Media from PLOS ONE