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双标荧光免疫细胞化学

Double Labeling Fluorescent Immunocytochemistry.

作者信息

Rak Monika, Reiss Krzysztof

机构信息

Department of Cell Biology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University in Kraków, Kraków, Poland.

Departments of Medicine & Neurological Cancer Research, Louisiana Cancer Research Center, Louisiana State University Health Sciences Center, New Orleans, LA, USA.

出版信息

Methods Mol Biol. 2022;2422:147-161. doi: 10.1007/978-1-0716-1948-3_10.

Abstract

Fluorescent immunocytochemistry is a powerful technique based on detecting antigens. It leads to discoveries in cell composition and structure as well as its functioning by expanding knowledge on colocalization between its components. The potency of this method is based on findings in the areas of specific antibodies production, fluorescent labels, and microscopy. Since it merges different fields, it requires basic knowledge on all the steps that are needed in the procedure planning and implementation to be used properly and produce reliable results. Here we describe a protocol of LN-229 human glioblastoma cells double labeling of LC3 and IRS-1 proteins, highlighting the importance of some steps of the procedure and possible variables.

摘要

荧光免疫细胞化学是一种基于检测抗原的强大技术。通过扩展对其组成成分之间共定位的认识,它在细胞组成、结构及其功能方面带来了诸多发现。该方法的有效性基于在特异性抗体生产、荧光标记和显微镜检查等领域的研究成果。由于它融合了不同领域,因此在正确使用并产生可靠结果的程序规划和实施过程中,需要具备所有步骤的基础知识。在此,我们描述了一种对LN - 229人胶质母细胞瘤细胞中LC3和IRS - 1蛋白进行双重标记的方案,强调了该程序某些步骤的重要性以及可能的变量。

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