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Radioimmunoassay for ovine, caprine and bovine prolactin in plasma and tissue extracts

机译:血浆和组织提取物中绵羊,山羊和牛催乳激素的放射免疫分析

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摘要

1. A radioimmunoassay for ovine prolactin is described based on the inhibition of the reaction between 131I-labelled ovine prolactin and guinea-pig or rabbit antiserum to ovine prolactin. The extent of the reaction after a 4-day incubation period is determined by chromatoelectrophoresis or by adsorption of unchanged 131I-labelled ovine prolactin on charcoal. The sensitivity is equal to 5·9ng. of prolactin/ml. of plasma with chromatoelectrophoresis, or 0·2ng. of prolactin/ml. of tissue extracts with the charcoal separation. 2. A complete cross-reaction demonstrated between ovine prolactin and caprine pituitary extracts allows the assay to be used to measure caprine prolactin. The partial cross-reactions between ovine prolactin and bovine prolactin and between ovine prolactin and bovine pituitary extract differ, and an alteration in the immunological activity of bovine prolactin during its isolation is suggested. Bovine prolactin in plasma may be measured against a bovine pituitary extract as standard. No cross-reactions were demonstrated with pituitary extracts from a number of other species. The extent of the contamination of ovine and bovine growth hormone preparations by their respective prolactins is shown. 3. Dilutions of ovine and caprine plasma inhibit the reaction between 131I-labelled ovine prolactin and antiserum with the same characteristics as ovine prolactin. 4. The immunoreactive material in plasma fractionates on Sephadex G-200 and in sucrose density gradients as a single peak similar to that shown by freshly dissolved ovine prolactin. There is no evidence that ovine prolactin is bound to a plasma protein. 5. By suppressing prolactin secretion and assaying serial samples of plasma thereafter it is shown that the immunological activity of the surviving hormone becomes progressively altered with time. It is suggested that this alteration is usually not detected but introduces an element of uncertainty into the quantitative but not the qualitative value of the measurements obtained by reference to standard ovine prolactin.
机译:1.基于抑制131I标记的绵羊催乳素与豚鼠或兔子的血清对绵羊催乳素的反应,对绵羊催乳素进行了放射免疫测定。孵育4天后,反应程度通过色谱电泳或未改变的131I标记的绵羊催乳素在木炭上的吸附来确定。灵敏度等于5·9ng。催乳素/毫升。色谱电泳法测定血浆浓度,或0·2ng。催乳素/毫升。用木炭分离组织提取物。 2.绵羊催乳素与山羊垂体提取物之间的完全交叉反应证明该测定法可用于测量山羊催乳素。绵羊催乳素和牛催乳素之间以及绵羊催乳素和牛垂体提取物之间的部分交叉反应是不同的,并且建议在分离过程中改变牛催乳素的免疫活性。血浆中的牛催乳素可以针对牛垂体提取物作为标准进行测量。从许多其他物种的垂体提取物中未发现交叉反应。显示了它们各自的催乳激素对绵羊和牛生长激素制剂的污染程度。 3.绵羊和山羊血浆的稀释会抑制131I标记的绵羊催乳素和抗血清之间的反应,抗血清的作用与绵羊催乳素相同。 4.血浆中的免疫反应性物质在Sephadex G-200上进行分馏,在蔗糖密度梯度中作为单个峰,类似于新鲜溶解的绵羊催乳素所显示的峰。没有证据表明绵羊催乳素与血浆蛋白结合。 5.通过抑制催乳激素分泌并随后测定血浆系列样品,表明存活激素的免疫活性随时间逐渐改变。建议通常不会检测到这种变化,但会引入不确定性,这是参考标准催乳素获得的测量值的定量值而非定性值。

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