供应WHO09/264可溯源血浆纤维蛋白原国际标准物质

供应WHO09/264可溯源血浆纤维蛋白原国际标准物质

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The WHO 3rd International Standard for Fibrinogen Plasma, consists of glass ampoules, coded 09/264, containing 1ml aliquots of a freeze-dried solvent-detergent treated pooled normal human plasma. This preparation was established by the Expert Committee on Biological Standardization of the World Health Organization in October 2011 and details of the preparation and value assignment are available in document WHO/BS/2011.2168. This standard is intended to be used in the measurement of fibrinogen in plasma and is primariliy intended for calibration of secondary and/or in-house working standards of fibrinogen plasma. WHO09/264

This preparation is not for administration to humans or animals in the human food chain.

The preparation contains material of human origin, and either the final product or the source materials, from which it is derived, have been tested and found negative for HBsAg, anti-HIV and HCV RNA. As with all materials of biological origin, this preparation should be regarded as potentially hazardous to health. It should be used and discarded according to your own laboratory’s safety procedures. Such safety procedures should include the wearing of protective gloves and avoiding the generation of aerosols. Care should be exercised in opening ampoules or vials, to avoid cuts. 可溯源血浆纤维蛋白原国际标准物质

世界卫生组织第三份纤维蛋白原血浆国际标准由玻璃安瓿组成,编号为09/264,含有1ml等分的冻干溶剂洗涤剂处理的正常人血浆。该制剂由世界卫生组织生物标准化专家委员会于2011年10月建立,制剂和价值分配的详细信息见世界卫生组织/英国标准2011.2168号文件。本标准旨在用于测量血浆中的纤维蛋白原,主要用于校准纤维蛋白原血浆的二级和/或内部工作标准。

该制剂不适用于人类或人类食物链中的动物。

该制剂含有人类来源的材料,其最终产物或来源材料经过测试,发现HBsAg、抗HIV和HCV RNA呈阴性。与所有生物来源的材料一样,这种制剂应被视为对健康有潜在危害。应根据您自己实验室的安全程序使用和丢弃它。此类安全程序应包括佩戴防护手套和避免产生气溶胶。打开安瓿或小瓶时应小心,以避免割伤。