van der Laak Jeroen A W M, Dijkman Henry B P M, Pahlplatz Martin M M
Department of Pathology 846, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.
Ultramicroscopy. 2006 Mar;106(4-5):255-60. doi: 10.1016/j.ultramic.2005.08.001. Epub 2005 Nov 2.
The magnification factor in transmission electron microscopy is not very precise, hampering for instance quantitative analysis of specimens. Calibration of the magnification is usually performed interactively using replica specimens, containing line or grating patterns with known spacing. In the present study, a procedure is described for automated magnification calibration using digital images of a line replica. This procedure is based on analysis of the power spectrum of Fourier transformed replica images, and is compared to interactive measurement in the same images. Images were used with magnification ranging from 1,000 x to 200,000 x. The automated procedure deviated on average 0.10% from interactive measurements. Especially for catalase replicas, the coefficient of variation of automated measurement was considerably smaller (average 0.28%) compared to that of interactive measurement (average 3.5%). In conclusion, calibration of the magnification in digital images from transmission electron microscopy may be performed automatically, using the procedure presented here, with high precision and accuracy.
透射电子显微镜中的放大倍数并不十分精确,例如这会妨碍对标本进行定量分析。放大倍数的校准通常使用包含已知间距的线条或光栅图案的复型标本以交互方式进行。在本研究中,描述了一种使用线条复型的数字图像进行自动放大倍数校准的程序。该程序基于对傅里叶变换后的复型图像功率谱的分析,并与同一图像中的交互测量进行了比较。使用了放大倍数范围从1000倍到200000倍的图像。自动程序与交互测量的平均偏差为0.10%。特别是对于过氧化氢酶复型,自动测量的变异系数相比交互测量(平均3.5%)要小得多(平均0.28%)。总之,使用此处介绍的程序,可以高精度和准确性地自动对透射电子显微镜数字图像中的放大倍数进行校准。