{"title":"Non-competitive time-resolved immunofluorometric assays for determination of human insulin-like growth factor I and II.","authors":"J Frystyk, B Dinesen, H Orskov","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We present sensitive non-competitive time-resolved immunofluorometric assays (TR-IFMAs) for IGF-I and IGF-II based on monoclonal antibodies. Assays were performed in microtest-plate wells: the first antibodies were immobilized on the solid matrix, the second labelled with the chelate derivative of Europium (Eu3+). The obtained specificities and sensitivities were high: IGF-I and IGF-II cross-reactivity in heterologous assay was below 0.0002%. The detection limits were 0.0025 micrograms/l and 0.010 micrograms/l for the IGF-I and IGF-II assay, respectively. The operating range included upwards: 2.5 micrograms/l (IGF-I) and 10.0 micrograms/l (IGF-II). This implies that all clinically relevant serum concentrations could be measured in one final dilution (1:1066 for IGF-I and 1:2132 for IGF-II) after acid ethanol extraction. The high sample dilution with buffer made further neutralization or evaporation of serum acid ethanol extracts unnecessary. Interassay variation of the assays was below 10%.</p>","PeriodicalId":77148,"journal":{"name":"Growth regulation","volume":"5 4","pages":"169-76"},"PeriodicalIF":0.0000,"publicationDate":"1995-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Growth regulation","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We present sensitive non-competitive time-resolved immunofluorometric assays (TR-IFMAs) for IGF-I and IGF-II based on monoclonal antibodies. Assays were performed in microtest-plate wells: the first antibodies were immobilized on the solid matrix, the second labelled with the chelate derivative of Europium (Eu3+). The obtained specificities and sensitivities were high: IGF-I and IGF-II cross-reactivity in heterologous assay was below 0.0002%. The detection limits were 0.0025 micrograms/l and 0.010 micrograms/l for the IGF-I and IGF-II assay, respectively. The operating range included upwards: 2.5 micrograms/l (IGF-I) and 10.0 micrograms/l (IGF-II). This implies that all clinically relevant serum concentrations could be measured in one final dilution (1:1066 for IGF-I and 1:2132 for IGF-II) after acid ethanol extraction. The high sample dilution with buffer made further neutralization or evaporation of serum acid ethanol extracts unnecessary. Interassay variation of the assays was below 10%.