Non-competitive time-resolved immunofluorometric assays for determination of human insulin-like growth factor I and II.

Growth regulation Pub Date : 1995-12-01
J Frystyk, B Dinesen, H Orskov
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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%.

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测定人胰岛素样生长因子I和II的非竞争时间分辨免疫荧光测定法。
我们提出了基于单克隆抗体的IGF-I和IGF-II的非竞争性时间分辨免疫荧光测定法(TR-IFMAs)。实验在微孔板中进行:第一抗体固定在固体基质上,第二抗体用铕(Eu3+)的螯合衍生物标记。所获得的IGF-I和IGF-II在异源检测中的交叉反应性低于0.0002%。IGF-I和IGF-II的检出限分别为0.0025微克/l和0.010微克/l。工作范围为2.5微克/升(IGF-I)和10.0微克/升(IGF-II)。这意味着在酸乙醇提取后,所有临床相关的血清浓度都可以在一次最终稀释(IGF-I为1:10 . 66,IGF-II为1:2 . 132)中测量。缓冲液对样品的高度稀释使得血清酸性乙醇提取物无需进一步中和或蒸发。测定结果的测定间变异小于10%。
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