| dc.contributor.author |
Hernandez, M |
en |
| dc.contributor.author |
Kisaalita, WS |
en |
| dc.contributor.author |
Farmer, MA |
en |
| dc.date.accessioned |
2014-06-06T06:43:01Z |
|
| dc.date.available |
2014-06-06T06:43:01Z |
|
| dc.date.issued |
1996 |
en |
| dc.identifier.issn |
10530509 |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/954 |
|
| dc.relation.uri |
http://www.scopus.com/inward/record.url?eid=2-s2.0-0012245404&partnerID=40&md5=e08a35dbc609b7c4ee60cfc619c24471 |
en |
| dc.subject |
Confocal microscopy |
en |
| dc.subject |
N1E-115 |
en |
| dc.subject |
Neuroblastoma |
en |
| dc.subject |
Resting membrane potential |
en |
| dc.subject |
Tetramethylrhodamine methyl ester |
en |
| dc.title |
Assessment of murine neuroblastoma (N1E-115) resting membrane potential by confocal microscopy |
en |
| heal.type |
journalArticle |
en |
| heal.publicationDate |
1996 |
en |
| heal.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 average V 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-115 V m was found to be sensitive, reproducible, fast, and simple. © 1996 Plenum Publishing Corporation. |
en |
| heal.journalName |
Journal of Fluorescence |
en |
| dc.identifier.issue |
2 |
en |
| dc.identifier.volume |
6 |
en |
| dc.identifier.spage |
77 |
en |
| dc.identifier.epage |
82 |
en |