Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI

Live Cell Imaging and Analysis Image Acquisition Live cell imaging and Image acquisition set up were exactly followed as per our previously published protocols (Fuseler and Valarmathi, 2012). “Following creation of the wound area in the MSCs monolayer cultures, the MatTek dishes were immediately mou...

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Main Author: Fuseler, John W.
Format: Article in Journal/Newspaper
Language:unknown
Published: figshare 2016
Subjects:
Online Access:https://dx.doi.org/10.6084/m9.figshare.4012428.v1
https://figshare.com/articles/media/Valarmathi_-_Video_-_3_-_MSCs-200_uM_SNAP-SN-2-24_Hours-10X_Ph_AVI/4012428/1
id ftdatacite:10.6084/m9.figshare.4012428.v1
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spelling ftdatacite:10.6084/m9.figshare.4012428.v1 2023-05-15T17:53:58+02:00 Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI Fuseler, John W. 2016 https://dx.doi.org/10.6084/m9.figshare.4012428.v1 https://figshare.com/articles/media/Valarmathi_-_Video_-_3_-_MSCs-200_uM_SNAP-SN-2-24_Hours-10X_Ph_AVI/4012428/1 unknown figshare https://dx.doi.org/10.6084/m9.figshare.4012428 Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode cc-by-4.0 CC-BY Stem Cells article MediaObject Media Audiovisual 2016 ftdatacite https://doi.org/10.6084/m9.figshare.4012428.v1 https://doi.org/10.6084/m9.figshare.4012428 2021-11-05T12:55:41Z Live Cell Imaging and Analysis Image Acquisition Live cell imaging and Image acquisition set up were exactly followed as per our previously published protocols (Fuseler and Valarmathi, 2012). “Following creation of the wound area in the MSCs monolayer cultures, the MatTek dishes were immediately mounted on the stage of a Zeiss Axiovert 200M inverted microscope in a Zeiss M200 humidified incubator chamber, and maintained at 37 o C and 5% CO 2 during the course of observations and the collection of images. An appropriate area of the margin of the wound was selected for imaging. Images were collected by time-lapse microscopy using phase contrast optics (10X, N.A. 0.25 PH-1 Achroplan objective) and a CCD camera (Hamamatsu ORCA-ER) controlled by Kinetic Imaging Image Acquisition Software (AQM Advance-6) software at a rate of 10 frames per hour for a total period of 24 hours. The incident light during exposure of the image was filtered with 546 nm green interference filter, and exposure times were maintained constant at 23.15 ms for all kinetic cell migration experiments,” (Fuseler and Valarmathi, 2012). Measurement of MSCs Cellular Movements and Displacements The effect of exogenous NO on directed cellular movement was determined by measurement of the displacement of individual MSCs into the wound region. The changes in the displacement of individual MSCs were determined by frame-by-frame analysis with the AQM Advance-6 software, and were expressed as the mean of the final displacement of the MSCs from the wound margin at 24 hours. On an average, 50 cells were measured for each experimental group treated with SNAP (SN-1 and SN-2) and their corresponding control groups. Article in Journal/Newspaper Orca DataCite Metadata Store (German National Library of Science and Technology)
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Stem Cells
spellingShingle Stem Cells
Fuseler, John W.
Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI
topic_facet Stem Cells
description Live Cell Imaging and Analysis Image Acquisition Live cell imaging and Image acquisition set up were exactly followed as per our previously published protocols (Fuseler and Valarmathi, 2012). “Following creation of the wound area in the MSCs monolayer cultures, the MatTek dishes were immediately mounted on the stage of a Zeiss Axiovert 200M inverted microscope in a Zeiss M200 humidified incubator chamber, and maintained at 37 o C and 5% CO 2 during the course of observations and the collection of images. An appropriate area of the margin of the wound was selected for imaging. Images were collected by time-lapse microscopy using phase contrast optics (10X, N.A. 0.25 PH-1 Achroplan objective) and a CCD camera (Hamamatsu ORCA-ER) controlled by Kinetic Imaging Image Acquisition Software (AQM Advance-6) software at a rate of 10 frames per hour for a total period of 24 hours. The incident light during exposure of the image was filtered with 546 nm green interference filter, and exposure times were maintained constant at 23.15 ms for all kinetic cell migration experiments,” (Fuseler and Valarmathi, 2012). Measurement of MSCs Cellular Movements and Displacements The effect of exogenous NO on directed cellular movement was determined by measurement of the displacement of individual MSCs into the wound region. The changes in the displacement of individual MSCs were determined by frame-by-frame analysis with the AQM Advance-6 software, and were expressed as the mean of the final displacement of the MSCs from the wound margin at 24 hours. On an average, 50 cells were measured for each experimental group treated with SNAP (SN-1 and SN-2) and their corresponding control groups.
format Article in Journal/Newspaper
author Fuseler, John W.
author_facet Fuseler, John W.
author_sort Fuseler, John W.
title Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI
title_short Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI
title_full Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI
title_fullStr Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI
title_full_unstemmed Valarmathi - Video - 3 - MSCs-200 uM SNAP-SN-2-24 Hours-10X Ph.AVI
title_sort valarmathi - video - 3 - mscs-200 um snap-sn-2-24 hours-10x ph.avi
publisher figshare
publishDate 2016
url https://dx.doi.org/10.6084/m9.figshare.4012428.v1
https://figshare.com/articles/media/Valarmathi_-_Video_-_3_-_MSCs-200_uM_SNAP-SN-2-24_Hours-10X_Ph_AVI/4012428/1
genre Orca
genre_facet Orca
op_relation https://dx.doi.org/10.6084/m9.figshare.4012428
op_rights Creative Commons Attribution 4.0 International
https://creativecommons.org/licenses/by/4.0/legalcode
cc-by-4.0
op_rightsnorm CC-BY
op_doi https://doi.org/10.6084/m9.figshare.4012428.v1
https://doi.org/10.6084/m9.figshare.4012428
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