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磷酸钙转染

Calcium phosphate transfection.

作者信息

Kingston R E, Chen C A, Okayama H

机构信息

Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Curr Protoc Immunol. 2001 May;Chapter 10:Unit 10.13. doi: 10.1002/0471142735.im1013s31.

Abstract

This unit contains two methods of calcium phosphate-based eukaryotic cell transfection, protocols that can be used for both transient and stable transfections. In the protocols, plasmid DNA is introduced to monolayer cell cultures via a precipitate that adheres to the cell surface. The Basic Protocol uses a HEPES-buffered solution to form a calcium phosphate precipitate that is directly layered onto the cells. In the alternate high-efficiency method, a BES-buffered system is used that allows the precipitate to form gradually in the medium and is then dropped onto the cells. The alternate method is particularly efficient for stable transformation of cells with circular plasmid DNA, and may be helpful with linear or genomic DNA. Both methods of transfection require very high-quality plasmid DNA, which can be prepared as described in the second Support Protocol. Transfection efficiency in some cell lines can be increased by shocking the cells with glycerol or dimethyl sulfoxide (DMSO) as described in the first Support Protocol.

摘要

本单元包含两种基于磷酸钙的真核细胞转染方法,这些方案可用于瞬时转染和稳定转染。在这些方案中,质粒DNA通过附着在细胞表面的沉淀物被引入单层细胞培养物中。基本方案使用HEPES缓冲溶液形成磷酸钙沉淀物,该沉淀物直接铺在细胞上。在另一种高效方法中,使用BES缓冲系统,使沉淀物在培养基中逐渐形成,然后滴加到细胞上。另一种方法对于用环状质粒DNA稳定转化细胞特别有效,对线性或基因组DNA可能也有帮助。两种转染方法都需要非常高质量的质粒DNA,可按照第二个支持方案所述进行制备。如第一个支持方案所述,用甘油或二甲基亚砜(DMSO)对细胞进行电击可提高某些细胞系的转染效率。

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