Adzemovic Milena Z, Zeitelhofer Manuel, Leisser Marianne, Köck Ulricke, Kury Angela, Olsson Tomas
Department of Clinical Neuroscience, Neuroimmunology Unit, Center for Molecular Medicine, Karolinska Institutet; Department of Neuroimmunology, Center for Brain Research, Medical University of Vienna;
Department of Clinical Neuroscience, Neuroimmunology Unit, Center for Molecular Medicine, Karolinska Institutet; Department of Medical Biochemistry and Biophysics, Vascular Biology Unit, Karolinska Institutet.
J Vis Exp. 2016 Nov 14(117):50425. doi: 10.3791/50425.
Immunohistochemistry (IHC) provides highly specific, reliable and attractive protein visualization. Correct performance and interpretation of an IHC-based multicolor labeling is challenging, especially when utilized for assessing interrelations between target proteins in the tissue with a high fat content such as the central nervous system (CNS). Our protocol represents a refinement of the standard immunolabeling technique particularly adjusted for detection of both structural and soluble proteins in the rat CNS and peripheral lymph nodes (LN) affected by neuroinflammation. Nonetheless, with or without further modifications, our protocol could likely be used for detection of other related protein targets, even in other organs and species than here presented.
免疫组织化学(IHC)可提供高度特异性、可靠且吸引人的蛋白质可视化。基于IHC的多色标记的正确操作和解读具有挑战性,尤其是当用于评估高脂肪含量组织(如中枢神经系统(CNS))中靶蛋白之间的相互关系时。我们的方案是对标准免疫标记技术的改进,特别针对受神经炎症影响的大鼠中枢神经系统和外周淋巴结(LN)中结构蛋白和可溶性蛋白的检测进行了调整。尽管如此,无论是否进一步修改,我们的方案可能都可用于检测其他相关蛋白靶点,甚至适用于本文未提及的其他器官和物种。