Mosedale D E, Metcalfe J C, Grainger D J
Department of Biochemistry, University of Cambridge, United Kingdom.
J Histochem Cytochem. 1996 Sep;44(9):1043-50. doi: 10.1177/44.9.8773570.
There is a growing trend towards the objective quantification of immunohistochemical staining. However, quantification has not been used previously to optimize the original published immunohistochemical methods. We present a quantitative method for analyzing immunofluorescence staining employing the Applied Imaging MAGISCAN image analysis system, which has then been used to optimize major aspects of the standard immunofluorescent staining protocols. The optimization process resulted in a method that increased specific staining up to fivefold over typical published protocols, with no increase in nonspecific staining. The method is extremely reproducible. For slides stained by a single experimenter in one batch on one day, the coefficient of variation between replicate means is 1.2%. The image analysis protocol gave a linear response with increasing antigen concentration, as determined by using purified antigen dried onto slides. The revisions to the standard protocol presented here can also be applied to nonquantitative staining. It will help users of immunofluorescence to maximize their staining and may enable the detection of previously undetected antigens.
免疫组织化学染色的客观定量分析趋势日益明显。然而,此前定量分析尚未用于优化最初发表的免疫组织化学方法。我们介绍一种使用Applied Imaging MAGISCAN图像分析系统分析免疫荧光染色的定量方法,该方法随后被用于优化标准免疫荧光染色方案的主要方面。优化过程产生了一种方法,其特异性染色比典型发表方案提高了五倍,非特异性染色没有增加。该方法具有极高的可重复性。对于由一名实验人员在一天内一批染色的玻片,重复平均值之间的变异系数为1.2%。通过使用干燥在玻片上的纯化抗原确定,图像分析方案随抗原浓度增加呈线性反应。此处介绍的对标准方案的修订也可应用于非定量染色。它将帮助免疫荧光使用者最大化染色效果,并可能使检测到以前未检测到的抗原成为可能。