哺乳动物细胞培养系统中基因定位和比较分析的细胞遗传学方法

William S. Modi , William G. Nash , Anna C. Ferrari , Stephen J. O'Brien
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引用次数: 48

摘要

这里介绍了我们实验室用于人类、家猫和其他哺乳动物的基因定位和细胞遗传学分析的详细方法。程序包括:1)建立原代成纤维细胞和淋巴样细胞培养;2)异种细胞融合制备快速增殖的细胞杂种;3)利用致癌逆转录病毒对原代成纤维细胞进行细胞转化;4)前中期染色体高分辨率带的细胞同步;5)染色体显带程序,包括g显带、碱性G-11和q显带;6)放射性标记分子克隆与中期染色体原位杂交,进行区域基因定位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytogenetic methodologies for gene mapping and comparative analyses in mammalian cell culture systems

Presented here are the detailed methods employed in our laboratory for gene mapping and cytogenetic analyses in human beings, in the domestic cat, and in other mammalian species. Included in the procedures are: 1) establishment of primary fibroblast and lymphoid cell cultures; 2) heterologous cell fusion for production of rapidly proliferating cell hybrids; 3) cellular transformation of primary fibroblasts using an oncogenic retrovirus; 4) cell synchronization for high-resolution banding of prometaphase chromosomes; 5) chromosome-banding procedures, including G-banding, alkaline G-11, and Q-banding; and 6) in situ hybridization of radiolabeled molecular clones to metaphase chromosomes for regional gene localization.

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