Greenfield Edward A
Cold Spring Harb Protoc. 2020 Oct 1;2020(10):2020/10/pdb.prot103317. doi: 10.1101/pdb.prot103317.
For most immunochemical methods, tissue culture supernatants will be the most useful source of monoclonal antibodies. The supernatants are not contaminated with high levels of other antibodies, and the concentration is high enough for most assays if used undiluted. This protocol describes the procedure of collecting tissue culture supernatants. When collecting supernatants for antibodies, allow the individual cultures to grow until the hybridomas die. This will allow collection of higher-titer supernatants. In general, antibodies are resistant to the proteases that are released from dying cells, so allowing the cells to die should not affect the quality of the antibodies. If extraneous IgG molecules will alter any of the assays for which the supernatants are being prepared, use medium with fetal bovine serum or use serum-free medium. The yield of this method is ∼20-50 µg of antibody/mL of supernatant. The most common problem encountered in storage of tissue culture supernatants after collection is contamination with bacteria or fungi. This can be prevented by the addition of sodium azide as described.
对于大多数免疫化学方法而言,组织培养上清液将是单克隆抗体最有用的来源。上清液不会被高水平的其他抗体污染,并且如果不稀释使用,其浓度对于大多数检测来说足够高。本方案描述了收集组织培养上清液的步骤。当收集抗体的上清液时,让各个培养物生长至杂交瘤细胞死亡。这将使得能够收集到效价更高的上清液。一般来说,抗体对垂死细胞释放的蛋白酶具有抗性,因此让细胞死亡不应影响抗体的质量。如果制备上清液所用于的任何检测会受到外来IgG分子的影响,可以使用含有胎牛血清的培养基或无血清培养基。该方法的产量约为每毫升上清液20 - 50微克抗体。收集后组织培养上清液储存过程中最常见的问题是被细菌或真菌污染。如所述,添加叠氮化钠可防止这种情况发生。