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Procedure for selection of cell clones to submerged cultures.

机译:选择细胞克隆至深层培养的程序。

摘要

In this process, a range of individual devices which are known per se are employed jointly to increase the number of cell clones to be tested per unit of time, in which process a) sterile microtitre plates are charged automatically with nutrient solutions under sterile conditions; b) each well of the microtitre plate is automatically inoculated with one cell; c) the inoculated microtitre plates are stacked and, in a shaker incubator incubated under submerged-culture conditions; d) a filtrate of the nutrient solution or an extract of the cell culture is prepared, and, in this filtrate or extract, the amount of the desired metabolic product is measured by a method known per se.
机译:在该方法中,联合使用一系列本身已知的单独设备以增加每单位时间要测试的细胞克隆的数量,其中a)在无菌条件下自动向无菌微量滴定板中加入营养液; b)微量滴定板的每个孔自动接种一个细胞; c)将接种的微量滴定板叠放,并在振动培养箱中于深层培养条件下孵育; d)制备营养液的滤液或细胞培养物的提取物,并且在该滤液或提取物中,通过本身已知的方法测量所需代谢产物的量。

著录项

  • 公开/公告号ES517112A0

    专利类型

  • 公开/公告日1983-08-01

    原文格式PDF

  • 申请/专利权人 HOECHST AKTIENGESELLSCHAFT;

    申请/专利号ES19820517112

  • 发明设计人

    申请日1982-11-04

  • 分类号C12Q1/04;C12Q1/24;C12N1/00;G01N33/54;

  • 国家 ES

  • 入库时间 2022-08-22 10:46:49

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