File:Distinct-External-Signals-Trigger-Sequential-Release-of-Apical-Organelles-during-Erythrocyte-ppat.1000746.s015.ogv
Distinct-External-Signals-Trigger-Sequential-Release-of-Apical-Organelles-during-Erythrocyte-ppat.1000746.s015.ogv (Ogg Theora video file, length 12 s, 99 × 99 pixels, 66 kbps, file size: 93 KB)
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editDescriptionDistinct-External-Signals-Trigger-Sequential-Release-of-Apical-Organelles-during-Erythrocyte-ppat.1000746.s015.ogv |
English: Calcium levels during schizont rupture and erythrocyte invasion by P. falciparum merozoites. P. falciparum late stage schizonts were labeled with Fluo-4AM and added to erythrocytes to allow reinvasion. Both DIC and fluorescence images were acquired simultaneously on a Zeiss LSM510 confocal microscope at 2 second intervals with a 63×, 1.4 NA lens, using 488 nm excitation at low power to minimize bleaching and cell damage. Fluorescence images are shown. |
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Source | Video S2 from Singh S, Alam M, Pal-Bhowmick I, Brzostowski J, Chitnis C (2010). "Distinct External Signals Trigger Sequential Release of Apical Organelles during Erythrocyte Invasion by Malaria Parasites". PLOS Pathogens. DOI:10.1371/journal.ppat.1000746. PMID 20140184. PMC: 2816683. | |||
Author | Singh S, Alam M, Pal-Bhowmick I, Brzostowski J, Chitnis C | |||
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 19:38, 12 October 2016 | 12 s, 99 × 99 (93 KB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Author | Singh S, Alam M, Pal-Bhowmick I, Brzostowski J, Chitnis C |
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Usage terms | http://creativecommons.org/publicdomain/zero/1.0/ |
Image title | Calcium levels during schizont rupture and erythrocyte invasion by P. falciparum merozoites. P. falciparum late stage schizonts were labeled with Fluo-4AM and added to erythrocytes to allow reinvasion. Both DIC and fluorescence images were acquired simultaneously on a Zeiss LSM510 confocal microscope at 2 second intervals with a 63×, 1.4 NA lens, using 488 nm excitation at low power to minimize bleaching and cell damage. Fluorescence images are shown. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2010-02 |