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使用原代细胞培养物或组织切片的快速免疫荧光筛选程序。

Rapid immunofluorescent screening procedure using primary cell cultures or tissue sections.

作者信息

Furst A, Mahowald A P

出版信息

J Immunol Methods. 1984 May 11;70(1):101-9. doi: 10.1016/0022-1759(84)90394-6.

DOI:10.1016/0022-1759(84)90394-6
PMID:6201560
Abstract

We describe a rapid procedure for immunofluorescent screening of hybridoma supernatants. Use of primary cell cultures as substrates allows immediate detection and partial characterization of antibodies binding selectively to specific cell types. Sulfonated tissue culture cluster lids are used as a single substrate upon which cells are cultured and all stages of the antibody binding assay are performed, including microscopic observation. They may also be used for mounting cryostat sections of tissues. Condensation rings on the lids isolate individual groups of cells for each assay. Cells may be live or fixed, as desired. Very small volumes of culture supernatant are required for each assay, and nearly all steps are performed in bulk.

摘要

我们描述了一种用于杂交瘤上清液免疫荧光筛选的快速方法。使用原代细胞培养物作为底物可立即检测并部分鉴定选择性结合特定细胞类型的抗体。磺化组织培养板盖用作单个底物,在其上培养细胞并进行抗体结合测定的所有阶段,包括显微镜观察。它们还可用于固定组织切片的封片。盖子上的冷凝环可为每次测定分离单个细胞组。细胞可根据需要为活细胞或固定细胞。每次测定所需的培养上清液体积非常小,几乎所有步骤都可批量进行。

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High-throughput screening of hybridoma supernatants using multiplexed fluorescent cell barcoding on live cells.利用活细胞上的多重荧光细胞条形码技术对杂交瘤上清液进行高通量筛选。
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Immunoperoxidase slide assay (IPSA)--a new screening method for hybridoma supernatants directed against cell surface antigens compared to other binding assays.免疫过氧化物酶玻片检测法(IPSA)——一种针对杂交瘤细胞上清液中针对细胞表面抗原的新型筛选方法,并与其他结合检测法进行比较。
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