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一种用于建立B淋巴母细胞系的简单红细胞裂解方法。

A Simple Red Blood Cell Lysis Method for the Establishment of B Lymphoblastoid Cell Lines.

作者信息

Liu Xi, Xu Chongfeng, Duan Ziyuan

机构信息

Wuhan Institute of Virology, Chinese Academy of Sciences; Genetic Resources Center, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences.

Genetic Resources Center, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences.

出版信息

J Vis Exp. 2017 Jan 14(119):55191. doi: 10.3791/55191.

Abstract

A number of methods exist for the transformation of B lymphocytes by the Epstein Barr virus in vitro into immortalized cell lines. We have developed a new method with a powerful and simple strategy for the establishment of B-LCLs, the red blood cell lysis method. This method simplified the PBMC separation procedure with red blood cell removal, and used as little as 0.5 mL of whole blood for establishing EBV-immortalized cell lines, which can proliferate to large cell numbers in a relatively short amount time with a 100% success rate. The method is simple, reliable, time saving, and applicable to treating a large number of the clinical samples.

摘要

有多种方法可在体外通过爱泼斯坦-巴尔病毒将B淋巴细胞转化为永生化细胞系。我们开发了一种新方法,即红细胞裂解法,它具有强大且简单的策略来建立B淋巴母细胞系(B-LCLs)。该方法简化了去除红细胞的外周血单个核细胞(PBMC)分离程序,并且建立EBV永生化细胞系时仅需0.5 mL全血,能在相对较短的时间内增殖到大量细胞,成功率达100%。该方法简单、可靠、省时,适用于处理大量临床样本。

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Generation of lymphoblastoid cell lines (LCLs).淋巴母细胞系(LCLs)的生成。
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Isolation and immortalization of lymphocytes.淋巴细胞的分离与永生化
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本文引用的文献

3
Generation of Epstein-Barr Virus (EBV)-immortalized B cell lines.爱泼斯坦-巴尔病毒(EBV)永生化B细胞系的产生。
Curr Protoc Immunol. 2007 Feb;Chapter 7:7.22.1-7.22.4. doi: 10.1002/0471142735.im0722s76.
4
EBV Immortalization of human B lymphocytes separated from small volumes of cryo-preserved whole blood.
Int J Epidemiol. 2008 Apr;37 Suppl 1:i41-5. doi: 10.1093/ije/dym285.
10
Proteome analysis of Epstein-Barr virus-transformed B-lymphoblasts and the proteome database.
J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Apr 5;787(1):197-206. doi: 10.1016/s1570-0232(02)00495-6.

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