Tolivia Jorge, Navarro Ana, del Valle Eva, Perez Cristina, Ordoñez Cristina, Martínez Eva
Departamento de Morfología y Biología Celular, Facultad de Biología y Medicina, Universidad de Oviedo, Spain.
Anal Quant Cytol Histol. 2006 Feb;28(1):43-53.
To describe a simple method to achieve the differential selection and subsequent quantification of the strength signal using only one section.
Several methods for performing quantitative histochemistry, immunocytochemistry or hybridocytochemistry, without use of specific commercial image analysis systems, rely on pixel-counting algorithms, which do not provide information on the amount of chromogen present in the section. Other techniques use complex algorithms to calculate the cumulative signal strength using two consecutive sections. To separate the chromogen signal we used the "Color range" option of the Adobe Photoshop program, which provides a specific file for a particular chromogen selection that could be applied on similar sections. The measurement of the chromogen signal strength of the specific staining is achieved with the Scion Image software program.
The method described in this paper can also be applied to simultaneous detection of different signals on the same section or different parameters (area of particles, number of particles, etc.) when the "Analyze particles" tool of the Scion program is used.
描述一种仅使用一个切片实现强度信号差异选择及后续定量的简单方法。
几种不使用特定商业图像分析系统进行定量组织化学、免疫细胞化学或杂交细胞化学的方法依赖于像素计数算法,该算法无法提供切片中显色剂含量的信息。其他技术使用复杂算法通过两个连续切片计算累积信号强度。为分离显色剂信号,我们使用了Adobe Photoshop程序的“颜色范围”选项,它为特定显色剂选择提供一个特定文件,该文件可应用于相似切片。特定染色的显色剂信号强度测量通过Scion Image软件程序实现。
当使用Scion程序的“分析颗粒”工具时,本文所述方法也可应用于在同一切片上同时检测不同信号或不同参数(颗粒面积、颗粒数量等)。