Schnagl H Y, Boyle W
J Immunol Methods. 1978;24(1-2):79-88. doi: 10.1016/0022-1759(78)90089-3.
A micro-version of the 51Cr release assay for cytotoxic lymphocytes has been devised, which is conducted in Terasaki plates, in a total reaction volume of 8 microliter. The conditions necessary to make the microassay equivalent in sensitivity and reproducibility to the standard macroassay are described. In comparison with the standard macroassay, the microassay provides a 10-fold reduction in the number of effector cells employed and represents a 50-fold reduction in reaction volume. The assay has been particularly valuable in the saving of antisera when these are employed to block target cell lysis, or to selectively inactivate cells of a particular phenotype in the effector cell population.
已设计出一种用于细胞毒性淋巴细胞的51Cr释放测定法的微量版本,该方法在特拉萨基板中进行,总反应体积为8微升。描述了使微量测定法在灵敏度和可重复性方面与标准宏观测定法相当所需的条件。与标准宏观测定法相比,微量测定法使用的效应细胞数量减少了10倍,反应体积减少了50倍。当使用抗血清阻断靶细胞裂解或选择性灭活效应细胞群体中特定表型的细胞时,该测定法在节省抗血清方面特别有价值。