[Validation of the radioimmunoassay for rat luteinizing hormone (LH) (author's transl)].

Reproduccion Pub Date : 1980-04-01
A M Aranda Iriarte
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Abstract

A rat LH radioimmunoassay (RIA) using the immunoreactants provided by Dr Parlow on behalf of the Rat Pituitary Hormone Program of the NIAMDD of the NIH is described. The instructions suggested by the NIH have been modified in order to reach a higher sensitivity. It is possible to use prepipetted frozen standards and the same labelled antigen over a period of 1 month, or longer, after labelling, provided the preparation is purified immediately prior to its use. These procedures, as well as the addition of antibody and buffer simultaneously, shorten considerably the time spent on a given RIA and decrease the inter- and intra-assay variability. The specificity of the method is also described. There is good parallelism between the standard curve and serial dilutions of plasmas and hypophyses of rats. The RIA was validated physiologically by LH determination on plasmas obtained from animals submitted to different experimental situations in which a decrease (hypophysectomy) or increase (ovariectomy, LH-RH treatment, etc.) of this hormone is expected.

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[大鼠黄体生成素(LH)放射免疫测定法的验证[作者译]。
本文描述了使用Parlow博士代表美国国立卫生研究院NIAMDD大鼠垂体激素项目提供的免疫反应物进行大鼠LH放射免疫测定(RIA)。为了达到更高的灵敏度,美国国立卫生研究院建议的说明已经进行了修改。如果在使用前立即纯化,则可以在标记后1个月或更长时间内使用预吸的冷冻标准物和相同的标记抗原。这些程序,以及同时添加抗体和缓冲液,大大缩短了在给定RIA上花费的时间,并减少了测定间和测定内的可变性。还描述了该方法的特异性。标准曲线与大鼠血浆和垂体的连续稀释有很好的平行性。通过对不同实验条件下的动物血浆LH测定,从生理学上验证了RIA,在不同的实验条件下,预期该激素的减少(垂体切除)或增加(卵巢切除,LH- rh治疗等)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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