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一种用于哺乳动物细胞影印培养的改良程序,可基于基因表达筛选克隆。

A modified procedure for replica plating of mammalian cells allowing selection of clones based on gene expression.

作者信息

Hornsby P J, Yang L, Lala D S, Cheng C Y, Salmons B

机构信息

Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta 30912.

出版信息

Biotechniques. 1992 Feb;12(2):244-51.

PMID:1616718
Abstract

The polyester cloth replica-plating technique for selection of mammalian cell clones was modified by growing cells in colonies on a flexible polytetrafluoroethylene membrane and then transferring them completely to polyester cloth (27-microns mesh), from which a replica was made by allowing cells to transfer to a cloth of smaller pore size (17-microns mesh). Using this technique, two phenotype selection methods are demonstrated here: in situ hybridization for detection of a specific mRNA and a photographic film assay for detection of luciferase expression. Cells were transfected with pSV2AL-A delta 5' in which firefly luciferase cDNA is under the control of the simian virus 40 promoter. The luciferase assay was adapted for colonies on polyester cloth; cells were permeabilized with digitonin to allow access of ATP and luciferin to the cell without disruption of colonies. Clones selected for expression or nonexpression of luciferase by the photographic film assay were positive or negative for expression after isolation from the cloth replica and subsequent growth under conventional culture conditions. The replica-plating procedure described here should be generally applicable to most mammalian cell types. The ability to produce replicas of colonies, combined with in situ hybridization or assays that can be adapted to in situ detection, provides phenotype selection for clones based on gene expression independent of growth characteristics.

摘要

用于选择哺乳动物细胞克隆的聚酯布影印培养技术进行了改进,具体方法是让细胞在柔性聚四氟乙烯膜上形成集落生长,然后将它们完整转移到聚酯布(27微米筛孔)上,通过使细胞转移到孔径更小的布(17微米筛孔)上从聚酯布制作影印。利用该技术,本文展示了两种表型选择方法:用于检测特定mRNA的原位杂交和用于检测荧光素酶表达的感光胶片检测法。用pSV2AL-Aδ5'转染细胞,其中萤火虫荧光素酶cDNA受猴病毒40启动子控制。荧光素酶检测适用于聚酯布上的集落;用洋地黄皂苷使细胞透化,以便ATP和荧光素进入细胞而不破坏集落。通过感光胶片检测法选择的荧光素酶表达或不表达的克隆,在从布影印上分离并在常规培养条件下后续生长后,表达呈阳性或阴性。本文所述的影印培养程序通常应适用于大多数哺乳动物细胞类型。产生集落影印的能力,结合原位杂交或可适用于原位检测的检测方法,为基于基因表达而与生长特性无关的克隆提供了表型选择。

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