dc.contributor.author |
Agiamarnioti, K |
en |
dc.contributor.author |
Triantis, T |
en |
dc.contributor.author |
Papadopoulos, K |
en |
dc.contributor.author |
Dimotikali, D |
en |
dc.date.accessioned |
2014-03-01T01:54:04Z |
|
dc.date.available |
2014-03-01T01:54:04Z |
|
dc.date.issued |
2004 |
en |
dc.identifier.issn |
1318-0207 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/27177 |
|
dc.subject |
chemiluminescence |
en |
dc.subject |
acridinium salts |
en |
dc.subject |
biotin |
en |
dc.subject.classification |
Chemistry, Multidisciplinary |
en |
dc.subject.other |
IMMUNOASSAY |
en |
dc.subject.other |
ASSAY |
en |
dc.subject.other |
STABILITY |
en |
dc.subject.other |
HORMONE |
en |
dc.subject.other |
LABELS |
en |
dc.subject.other |
PROBES |
en |
dc.title |
Synthesis and chemiluminescent properties of novel biotinylated acridinium esters |
en |
heal.type |
journalArticle |
en |
heal.language |
English |
en |
heal.publicationDate |
2004 |
en |
heal.abstract |
Biotinylated acridinium ester, 9-(3-biotinyloxypropyl)-10-methylacridinium-9-carboxylate trifluoromethane sulphonate, 5 and its precursors, 9-(3-hydroxypropyl)-acridine-9-carboxylate 3 and 9-(3-biotinyloxypropyl)-acridine-9-carboxylate 4 were synthesized from acridine-9-carboxylic acid and were tested for their chemiluminescent properties. In contrast to aqueous solutions, in which the chemiluminescence is very low, in polar aprotic solvents such as N, N-dimethylformamide, it increases by a few orders of magnitude. The acridinium ester 5 as well as the precursors 3 and 4 could be detected down to few picomoles. |
en |
heal.publisher |
SLOVENSKO KEMIJSKO DRUSTVO |
en |
heal.journalName |
ACTA CHIMICA SLOVENICA |
en |
dc.identifier.isi |
ISI:000220368800008 |
en |
dc.identifier.volume |
51 |
en |
dc.identifier.issue |
1 |
en |
dc.identifier.spage |
67 |
en |
dc.identifier.epage |
76 |
en |