Assessment of Murine Neuroblastoma (N1E-115) Resting Membrane Potential by Confocal Microscopy
dc.contributor.author | Hernandez, Miguel | |
dc.contributor.author | Kisaalita, William S. | |
dc.contributor.author | Farmer, Mark A. | |
dc.date.accessioned | 2025-04-15T09:26:42Z | |
dc.date.available | 2025-04-15T09:26:42Z | |
dc.date.issued | 1996 | |
dc.description.abstract | Digital imaging (confocal microscopy) and a slow potentiometric dye (tetramethylrhodamine methyl ester) were used to assess the resting membrane potential (V m) of murine neuroblastoma cells (N1E-115). The averageV m was found to be −64.0±2.0 mV. The difference between this and the previously reported higher values was attributed to the use of glass microelectrode techniques that probably caused mechanical injury to the cell membranes: Digital imaging of N1E-115V m was found to be sensitive, reproducible, fast, and simple. | |
dc.identifier.citation | Hernandez, M., Kisaalita, W. S., & Farmer, M. A. (1996). Assessment of murine neuroblastoma (N1E-115) resting membrane potential by confocal microscopy. Journal of Fluorescence, 6, 77-82. | |
dc.identifier.uri | https://link.springer.com/article/10.1007/BF00732046 | |
dc.identifier.uri | https://nru.uncst.go.ug/handle/123456789/10667 | |
dc.language.iso | en | |
dc.publisher | Journal of Fluorescence | |
dc.title | Assessment of Murine Neuroblastoma (N1E-115) Resting Membrane Potential by Confocal Microscopy | |
dc.type | Article |
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