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培养的人胚肾细胞产物的生物测定问题:纤溶酶原激活剂

Problems in the bioassay of products from cultured HEK cells: plasminogen activator.

作者信息

Lewis M L, Morrison D R, Mieszkuc B J, Fessler D L

出版信息

Adv Exp Med Biol. 1984;172:241-67. doi: 10.1007/978-1-4615-9376-8_15.

Abstract

For research and commercial purposes, the production of materials from cultured cells is progressively becoming routine. Measuring products in cell culture medium, however, is not always straight-forward even when the most appropriate product assays are utilized. A researcher interested in a particular cell product does not intend to spend time developing or refining existing assays. Instead, he would prefer using techniques and standards reported in the literature. Evaluations of enzyme activity using purified standards or control products may inadvertently lead to the assumption that the same procedures will give reproducible results when cell culture medium is assayed for the product. This report describes the selection of commercially available lots of human embryonic kidney cells and the activity of the plasminogen activator (PA) produced by these cells. PA activity was measured by the fibrin plate assay. The problems of comparing activity in conditioned culture medium with that of purified standard preparations are presented. Factors contributing to non-linearity in dose response curves, inconsistencies in activity in replicate flask cultures, and variations in repeated assays after sample storage are considered. Sample handling procedures and alternate assay systems are discussed.

摘要

出于研究和商业目的,利用培养细胞生产材料正逐渐成为常规操作。然而,即便使用了最合适的产物分析方法,在细胞培养基中测量产物也并非总是简单直接的。对特定细胞产物感兴趣的研究人员并不打算花费时间去开发或完善现有的分析方法。相反,他更倾向于使用文献中报道的技术和标准。使用纯化标准品或对照产物对酶活性进行评估可能会无意中导致这样一种假设,即当对细胞培养基中的产物进行分析时,相同的程序会给出可重复的结果。本报告描述了市售人胚肾细胞批次的选择以及这些细胞产生的纤溶酶原激活剂(PA)的活性。通过纤维蛋白平板法测量PA活性。文中提出了比较条件培养基中的活性与纯化标准制剂活性时存在的问题。还考虑了导致剂量反应曲线非线性、重复培养瓶培养中活性不一致以及样品储存后重复分析结果存在差异的因素。讨论了样品处理程序和替代分析系统。

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