[国家卫生科学研究所人类绝经期促性腺激素参考标准(对照961)]。

M Ema, A Harazono, E Miyawaki, H Amano, Y Ogawa, S Okada
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引用次数: 0

摘要

对人绝经期促性腺激素(HMG)原料进行检测,制备“人绝经期促性腺激素参考标准(对照961)”。分别采用增强卵巢增重法和精囊增重法对照第三版尿促卵泡激素(FSH)和黄体生成素(LH)国际标准(71/264)测定候选材料的促卵泡激素(FSH)活性和促黄体生成素(LH)活性。新标准的效力被定义为每毫克56个国际单位的卵泡刺激素活性和每毫克61个国际单位的LH活性,这是四个合作实验室分别进行13次和5次测定的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The Human Menopausal Gonadotrophin Reference Standard (Control 961) of the National Institute of Health Sciences].

Raw human menopausal gonadotrophin (HMG) material was examined for preparation of the "Human Menopausal Gonadotrophin Reference Standard (Control 961)". The candidate material was assayed its follicle stimulating hormone (FSH) activity and luteinizing hormone (LH) activity against the 3rd International Standard for FSH and LH, urinary (71/264) by the augmented ovarian weight gain assay and the seminal vesicle weight gain test, respectively. The potency of the new standard was defined as 56 international units of FSH activity per mg and 61 international units of LH activity per mg as the result of 13 and 5 assays, respectively, in four collaborative laboratories.

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