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通过旋转粘附双免疫吸附试验(SADIST)快速筛选单克隆抗体。

Rapid screening of monoclonal antibodies by spin adherence double immunosorbent test (SADIST).

作者信息

Wyatt D M, Rylatt D B, Bundesen P G, Parish C R, Street G D

出版信息

J Immunol Methods. 1985 Feb 11;76(2):273-82. doi: 10.1016/0022-1759(85)90304-7.

Abstract

The spin adherence double immunosorbent test (SADIST) is a simple, rapid immunoassay with sensitivity similar to the enzyme-linked immunosorbent assay (ELISA). A 1-step SADIST has been found suitable for rapid screening of hybridomas for antigen-specific monoclonal antibodies (MAb). In this procedure hybridoma supernatants are added to antigen coated microplates followed by commercially available antiglobulin beads. The microplate is immediately centrifuged. Wells containing antigen-specific MAb produce a mat of beads whilst wells without antigen-specific MAb produce a button of beads. No washing or incubation steps are necessary and results are read within minutes of adding beads to test supernatants. By comparison, ELISA tests require several hours to perform with multiple wash steps and further reagent additions. A 2-step SADIST was also assessed. Supernatants are incubated in the microplate as for an ELISA and a wash step precedes the addition of antiglobulin beads. A panel of 117 hybridoma supernatants was selected to assess the suitability of the SADIST techniques for hybridoma screening. The supernatants were added to antigen-coated microplates and SADIST and ELISA tests performed. The SADIST correctly discriminated most hybridoma supernatants that were clearly positive or negative by ELISA. It was also found possible to perform SADIST followed by ELISA tests on the same microplate well without significantly affecting ELISA values.

摘要

自旋粘附双免疫吸附试验(SADIST)是一种简单、快速的免疫测定方法,其灵敏度与酶联免疫吸附测定(ELISA)相似。已发现一步法SADIST适用于快速筛选产生抗原特异性单克隆抗体(MAb)的杂交瘤。在此过程中,将杂交瘤上清液加入包被有抗原的微孔板中,随后加入市售的抗球蛋白珠。立即对微孔板进行离心。含有抗原特异性单克隆抗体的孔会产生一层珠状物,而不含抗原特异性单克隆抗体的孔会产生一团珠状物。无需洗涤或孵育步骤,在向测试上清液中加入珠子后的几分钟内即可读取结果。相比之下,ELISA检测需要几个小时才能完成,且有多个洗涤步骤并需添加更多试剂。还评估了两步法SADIST。上清液在微孔板中孵育,方式与ELISA相同,在加入抗球蛋白珠之前有一个洗涤步骤。选择了一组117种杂交瘤上清液来评估SADIST技术用于杂交瘤筛选的适用性。将上清液加入包被有抗原的微孔板中,并进行SADIST和ELISA检测。SADIST正确地区分了大多数通过ELISA明显呈阳性或阴性的杂交瘤上清液。还发现可以在同一微孔板孔中先进行SADIST,然后进行ELISA检测,而不会显著影响ELISA值。

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