pubmed-article:663956 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:663956 | lifeskim:mentions | umls-concept:C0021585 | lld:lifeskim |
pubmed-article:663956 | lifeskim:mentions | umls-concept:C0013494 | lld:lifeskim |
pubmed-article:663956 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:663956 | lifeskim:mentions | umls-concept:C0444498 | lld:lifeskim |
pubmed-article:663956 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:663956 | pubmed:dateCreated | 1978-9-1 | lld:pubmed |
pubmed-article:663956 | pubmed:abstractText | The possibility of quantitating insect ecdysones in situ on thin-layer chromatographic plates was examined. Two approaches were evaluated: 1) the induction of ecdysone fluorescence by sulfuric acid treatments and 2) the fluorescence-quenching of fluorescent thin-layer chromatographic plates by ecdysones. The fluorescence-quenching method was found to be most suitable and had a linear response range from 0.5 to 3 microgram for alpha-ecdysone and 20-hydroxyecdysone. Fluorescence-quenching and high pressure liquid chromatographic analyses obtained from extracts of alpha-ecdysone 20-hydroxylase incubations gave similar results. New data concerning the acid-induced fluorescence of ecdysones showed alpha-ecdysone to be twice as fluorescent as 20-hydroxyecdysone. | lld:pubmed |
pubmed-article:663956 | pubmed:language | eng | lld:pubmed |
pubmed-article:663956 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:663956 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:663956 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:663956 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:663956 | pubmed:month | Jan | lld:pubmed |
pubmed-article:663956 | pubmed:issn | 0039-128X | lld:pubmed |
pubmed-article:663956 | pubmed:author | pubmed-author:SvobodaJ AJA | lld:pubmed |
pubmed-article:663956 | pubmed:author | pubmed-author:MayerR TRT | lld:pubmed |
pubmed-article:663956 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:663956 | pubmed:volume | 31 | lld:pubmed |
pubmed-article:663956 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:663956 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:663956 | pubmed:pagination | 139-50 | lld:pubmed |
pubmed-article:663956 | pubmed:dateRevised | 2003-11-14 | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-A... | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-M... | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-M... | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-C... | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-E... | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-S... | lld:pubmed |
pubmed-article:663956 | pubmed:meshHeading | pubmed-meshheading:663956-S... | lld:pubmed |
pubmed-article:663956 | pubmed:year | 1978 | lld:pubmed |
pubmed-article:663956 | pubmed:articleTitle | Thin-layer chromatographic in situ analysis of insect ecdysones via fluorescence-quenching. | lld:pubmed |
pubmed-article:663956 | pubmed:publicationType | Journal Article | lld:pubmed |